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Provides clinical research management for the healthcare industry. See lists of services, locations, and upcoming trade shows.

A contract research organization providing analytical services to pharmaceutical companies.
Relationships to a whole new level. ABC offers a broad array of development services from IND-enabling programs to the full range of CMC analytical support. But it isn t what we do that makes us different than other contract service providers, it the way we manage our business with expert consulting services, professional program management, performance metrics and transparency. ABC Laboratories has been helping companies develop highly regulated products for more than 40 years. We ve seen

Full-service, therapeutically-focused CRO conducting phase I-IV trials for the pharmaceutical and biotechnology industries.

A progressive Clinical Trials Management Organization committed to providing superior service and quality data collection to the medical community.
ACR Idaho is now conveniently located west of St. Lukes Meridian Hospital, minutes away from the Boise airport and conveniently close to the I-84 freeway Eagle exit, in one of the most vibrantcommunities in the Rocky Mountain states. Our Boise office provides 3 large exam rooms, 2 monitoring rooms, secure medication area, dedicated laboratory, efficient coordinator and investigator work areas, including a private conference room and comprehensive electronic office support equipment.We appreciate

Operates two independent clinics in Canada for pharmacokinetic, bioequivalence, and pharmacology studies. An analytical laboratory offers clinical sample analysis.
Our reputation is largely due to our employees who have a wealth of scientific experience and through sharing our knowledge within the industry, we grow. See what we have accomplished!.

Group of scientific and medical professionals providing clinical research services to pharmaceutical and biotechnology industries.
Grass and tree pollens, and their circulating levels are maintained according to tight, quality-controlled standards. In order to simulate a heavy, in-season pollen day, subjects are exposed to allergens over a period of several hours. Unlike field studies, EEC studies can be run at any time of the year with little variation in pollen exposure. Studies typically utilize pre-established allergen levels known to induce allergic rhinoconjunctivitis symptoms at the moderate to severe level. The

Full-service contract research organization offering regulatory, clinical, reimbursement and compliance services to the medical device and biologic industries.
Executive, she oversees Alquest growing presence in the San Francisco Bay Area. Jill joined Alquest from Boston Scientific where sheserved as Director of Enteryx Clinical Research. Previously Jill served as Vice President, Clinical and Regulatory Affairs for Enteric Medical Technologies, Senior Manager of Clinical and Regulatory Affairs for Metra Biosystems, Senior Development Scientist for Dade-Behring Diagnostics, and Raw Material Chemist for Monoclonal Antibodies, Inc. Jill earned a B.S. in

Offers a full array of services to the pharmaceutical, biotech, medical device and medical diagnostic development industries. Services include phase I through IV development planning, protocol develo
Capable hands. We are a consultative group of clinical researchers, always ready to go out on the limb and give our own recommendations forsolving the challenges clients face over the course of a clinical development program or single trial. And of course we stand behind our recommendations by putting them into action ourselves through our CRO services. Amarex modest size, flat organizational structure and highly qualified staff assure that every project is guided by very experienced clinical

Strategic planning, clinical trial design and management, monitoring, and regulatory affairs services for emerging technologies in the drug, biopharmaceutical, and medical device industry.
Location. The site may include (but not be restricted to) metrics, timelines, study specific discussions and actual clinical data. This portal was created with the intention to improve project management by enhanced communications and allowing for earlier identification of possible issues..421 S. Lynnhaven Road, Suite 101, Virginia Beach, VA 23452 757-631-2114 757-631-2115 FAX info@arkios.421 S. Lynnhaven Road, Suite 101, Virginia Beach, VA 23452 757-631-2114 757-631-2115 FAX info@arkios.Topic

A specialty CRO focusing exclusively in monitoring clinical trials. Provides project teams as well as individual monitors for client directed projects.

An independent CRO (formerly Boston Biostatistics, Inc.) providing services such as clinical trials program planning and study design, clinical and medical monitoring, medical writing, database develo
Nombreuses societes pharmaceutiques ont commence la production active de divers generiques du Viagra les analogues du Viagra aux prix abordables. Aujourd hui les generiques du Viagra sont beaucoup plus populaires et mieux vendus que leurs homologues de marque. La base de tous les generiques du Viagra est le citrate de sildenafil qui est utilise comme un ingredient actif du Viagra de marque. Aujourd hui il y a beaucoup d hommes qui souffrent de la dysfonction erectile. Les medecins proposent un

A nationally recognized leader in clinical trial patient recruitment. We provide complete, creative marketing communications solutions for the healthcare medical marketplace.
Passages, and more recently with desktop publishing software like Aldus PageMaker including versions of Lorem Ipsum..Lorem Ipsum is simply dummy text of the printing and typesetting industry. Lorem Ipsum has been the industrys standard dummy text ever since the 1500s, when an unknown printer took a galley of type and scrambled it to make a type specimen book. It has survived not only five centuries, but also the leap into electronic typesetting, remaining essentially unchanged. It was

Delivering independent, scientific support to the pharmaceutical, chemical, agrochemical, food, drink, nutraceutical, consumer healthcare industries and government in assessing the health effects of d
Is considered by the registrant using a weight of evidence approach, and that a screening assessment is conducted initially in cases where only limited data are available in the dossier. Commission Regulations (EU) No. 252 2011 and 253 2011, both of 15 March 2011, amending Regulation (EC) No. 1907 2006 of the European Parliament and of the Council on the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH) as regards Annex I and Annex XIII, respectively..2011, L69, 3, 7

An independent health research facility specializing in comprehensive clinical trial management and coordination services for physicians, sponsors, clinical research coordinators and associates.

Dedicated to Phase I clinical trials, including first-in-man, dose-ranging, pharmacokinetic, bioavailability, drug interaction, and bioequivalence studies in healthy volunteers. Facility is located i
689 Warden Avenue, Units 1 2. Park at any available parking spot. The first entrance door (main entrance) is the entrance for volunteers scheduled for medical screening, and for study participants, staff and study sponsors..Biovail Contract Research will be exhibiting in the following conferences. Please visit us at our booth. If you would like to set up meeting with us, please contact our Business Development Teamt at, Sharon.Ramnarine@biovail, Greg.Downs@biovail,or Rick.Luque@biovail. Please

Company conducting routine and research driven analytical projects in support of drug-candidate discovery, pre-clinical, and clinical studies using advanced LC/MS/MS, GC/MS and HPLC methodologies.
Head Office BRI Biopharmaceutical Research Inc. 101 - 8898 Heather Street Vancouver, BC Canada V6P 3S8 Phone 604-432-9237 Fax 604-432-9239 Scientific Enquiry David Kwok, CEO Phone 604-432-9237 x225 Email dkwok@bripharm Business Development Clara Faan, VP Business Development Phone 604-432-9237 x224 Email cfaan@bripharm Sample Logistics Isabella Meng, Coordinator Phone 604-432-9237 x228 Email imeng@bripharm Regulatory Affairs Quality Assurance Rosario Bermudez, Manager Phone 604-432-9237 x233

Clinical trials management organization in Charlotte, North Carolina partners with board-certified local physicians to provide study management and administrative support for study sponsors.
Carolinas Research Associates is currently enrolling people in the following studies. If you qualify to participate, you may be paid for your time and travel expenses. Find out how by contacting us today..Carolinas Research Associates is currently enrolling people in the following studies. If you qualify to participate, you may be paid for your time and travel expenses. Find out how by contacting us today..Carolinas Research Associates is currently enrolling people in the following studies. If

A full-service, privately held contract research organization provides expertise in the development of drugs, biologics, medical devices, and nutrition products across a variety of therapeutic areas.
Full-service contract research and development organization with international resources dedicated to helping pharmaceutical and biotechnology companies efficiently and expeditiously navigate the regulatory approval process in order to bring new drugs, biologics, and medical devices to the people who need them. Cato Research Overview Contact Us.November 2, 2011 - Project Management for Biotech Companies In today& ,s fast paced, high pressure world of drug development there are multiple factors

Full service CRO with expertise in all areas of clinical research and drug development, including preclinical/nonclinical studies, clinical trial management, data management, regulatory services, qual
Technologies that we employ to build our customers optimal solution..All rights reserved. Use of this site indicates you accept the Terms of Use of this Site..If you breach any of these Terms, your authorization to use this Site automatically terminates and you must immediately destroy any downloaded or printed materials..CCS Associates welcomes inquiries and comments from visitors to this Site. However, any material, information or other communication you transmit or post to this Site or to CCS

Undertakes research projects on a contractual basis for industry, organizations, individuals, and governmental agencies.

Global contract central laboratory offering routine safety testing and esoteric method development and validation with full logistical support for local and global trials. Specialist in biomarkers an
Laboratories in Europe, USA and Asia, CentraLabS covers 80% of all clinical trial locations. CentraLabS has also assembled a qualified family of alliance laboratories and clinical service providers that provide an informed alternative choice for the support of global clinical studies in the rest of the world. CentraLabS implements a continual monitoring program to ensure the consistent quality of all our alliance partners. CentraLabS is committed to providing a true global laboratory service to

Global contract research organization based in California, focused on drug discovery. Overview of synthetic chemistry and screening capabilities, custom synthesis options, and related services.
150-250 mg per unit and average purity greater than 90%. ChemDiv is the partner of choice for screening libraries due to its experience in building a library of drug-like compounds that meet the criteria of the pharmaceutical industry& ,s hit-to-lead discovery process. ChemDiv produces both diverse and focused combinatorial libraries, as well as the proprietary building blocks. We permanently support discovery process of our customers with largest renewable pool of new Templates and Compounds.

Provides a full range of services for international and national management of clinical trials in Europe and North America.
Reserved. Registered in England and Wales No. 01636704. Registered Office 171 Bath Road, Slough, Berkshire, SL1 4AA, United Kingdom..SqlException (0x80131904) Conversion failed when converting the varchar value 25?v=xml to data type int. System.Data.SqlClient.SqlConnection.OnError(SqlException exception, Boolean breakConnection) +1953274 System.Data.SqlClient.SqlInternalConnection.OnError(SqlException exception, Boolean breakConnection) +4849707

Offers clinical research, pre-clinical GLP, laboratory assay development and central laboratory services to the biotechnology and pharmaceutical industry.
Development by sharing extensive experience in.Description An unhandled exception occurred during the execution of the current web request. Exception Details Alogient.Cameleon.Sdk.CMException Page doesn& ,t exist NavID=716, CultureCode=en-CA?v=xml Source Error.The following provisions constitute the Terms and Conditions of Use of CIRION Clinical Trial Services Inc. Web site.1. AcceptancePlease read this Legal Notice carefully before using this Web site. CIRION Clinical Trial Services Inc. and

Full service CRO specializing in monitoring and project management services.
Memorial Sloan Kettering Cancer Center in New York City within the Department of Medicine and Department of Psychiatry. She is certified as a Clinical Research Associate (CCRA) through the Association of Clinical Research Professionals and is founder and President of the Eastern Massachusetts Chapter of ACRP. She is a member of the following professional organizations ACRP , DIA, Society for Clinical Trials Inc. and SOCRA. In addition, she is a significant contributor to education within the

A full service clinical supplies CRO which employs a pharmacist's philosophy and comprehensively links the conventional services of logistics, packaging, labeling, distribution, and reconciliation und

An international company providing consultation and management services to the pharmaceutical, biotechnology and medical device industries. Includes company news, careers information and details of gl
Empresa in Buenos Aires, Argentina..

CRO specializing in web-based data management applications (eCRF), clinical monitoring, investigator training, safety reports (eSAE).

Conducting trials into the efficacy of psychiatric medications, with details of staff involved and a description of the process. Garden Grove, California, USA.
Neurobiological illness in which an individual is diagnosed with schizophrenia as well as a mood disorder, either manic elevated moods, or extreme depression. Individuals who suffer with this have periodic episodes of hallucinations, paranoid.

One of the world's largest and most comprehensive drug development services companies.
And most comprehensive drug development services companies with more than 10,000 employees in 60 countries. Through its nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today..Covance is one of the worlds largest and most comprehensive drug development services companies with more than 10,000 employees in 60 countries. Through its nonclinical, clinical and commercialization

Focuses on testing the safety and efficacy of pharmaceutical and consumer dermatologic products. Also has an operating division dedicated to molecular diagnostics, including pharmacogenomics, and prot
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Providing clinical trial monitoring and study management services to pharmaceutical, medical device and biotechnology companies in the US and Europe.
TeamTrials enables easier collaboration among all members of a clinical research team. TeamTrials isn t just an electronic version of a paper-based trial, it is designed to make every step of the clinical trial more efficient, to make every team member job a little easier. Naturally, TeamTrials supports open standards to enable smooth integration throughout the clinical development process..Emissary, TeamTrials,and the Compass Logo are registered trademarks..The first rumblings for US drug

Provides data collection services, computer systems development, and study monitoring. Rockville, Maryland, USA.

Provides biostatistics, epidemiology, data management and clinical trials support services. Atlanta, Georgia, USA.
Sire Records - Reactivated unit of Warner Music, with news and history of the label. Flash required..

A comprehensive contract research organization (CRO) that specializes in the neurosciences. Servicing the pharmaceutical, biotechnology and medical device industries.

Full service CRO that specializes in helping the pharmaceutical, biotech and medical device industry bring new cardiovascular medicines and devices to market. Special services include EKG, echo and H

A full-service CRO dedicated to providing clinical trials management and support to pharmaceutical companies for Phase I - IV clinical trials under FDA review since 1986.
Happening. Our first and foremost intention is for the well being of the patient. To participate in drug trial, an individual must first be diagnosed with the condition for which the trial is being conducted. This is can be done in one of two ways. They can either have their personal physician submit their records to the clinic for review, or have the clinic perform a physical examination and diagnosis. The content of the physical examination is totally dependent on the clinical drug trial. Once

Clinical Site Management Organization specializing in coordinating clinical studies.
Gulf Coast Research LLC has two offices in Louisiana. We contract with pharmaceutical companies (Sponsors) and Contract Research Organizations (CROs) to recruit, coordinate, and manage Phase I through Phase IV clinical trials throughout our vast and diverse network of Clinical Investigators in South Central Louisiana. Our highly efficient Research Center structure allows us to respond quickly to the Sponsor& ,s research needs. Our centralized management and coordination system produces

Offering services in informatics, medicinal chemistry, diagnostics, and clinical trials, with details of research facilities, products and services. Boston, Massachusetts, USA.
Clinical Pharmacology Started in year 2003, our service center is one of the largest in India. With a total of 264 beds spread across 7 clinics, GVK BIO is well.

Provides research, process development, analytical services and manufacturing for the pharmaceutical, dietary supplement and fine chemical industries. Includes details of facilities in Denver, Colorad
Polysaccharides, alkaloids, nucleosides, and saponins Anti-oxidants Plant proteins.The server encountered an internal error or misconfiguration and was unable to complete your request. Please contact the server administrator, no address given and inform them of the time the error occurred, and anything you might have done that may have caused the error..

Management and monitoring of clinical trials, as well as audits and development of standard operating procedures. Calgary, Alberta, Canada.
Voluntary inspections demonstrated the lack of these procedures and processes to be one of the most frequent deficiencies at the site level. The FDA asks to review SOPs when conducting site inspections, and sponsors are more frequently asking to review the sites SOPs prior to placing new clinical trial contracts with the institution, as a demonstration of the sites standards of practice. HRC& ,s SOPs The SOPs developed by the Hegi Research Group are written in compliance with the International

Providing the pharmaceutical & biotechnology industries with exceptional clinical research management & biometric services.
That our people are the most important asset. It is they who have helped to make ICON the success it is. Their commitment to clients, quality and delivery has earned ICON its enviable reputation..There something about the way we work that makes our clients come back for more. What we do, we do better. Our goal is to provide exceptional services to complete our clients clinical trials. These services include clinical research, biometrics, data management, interactive technologies, laboratory,

A therapeutically focused, full service contract research organization specializing in drug development services for drugs used to treat central nervous system (CNS) disorders and cancer.
Improving quality of life for patients around the world..2012 INC Research, LLC. All Rights Reserved.You have big ambitions for your products, so you need a partner that thinks big, too. At INC Research, we forge innovative and flexible strategic alliances that produce actionable data, enabling you to assess the potential of your products quickly and cost effectively while freeing your own resources to think about the next big thing. In fact, such alliances that have helped us contribute to the

Clinical services network which partners with pharmaceutical, device, and biomedical companies to provide innovative clinical operations solutions.
Developing and implementing quality assurance program for auditing clinical data, analyzing and interpreting data, generating final reports, coordinating medical, regulatory, and biostatistical consultant staff, preparing internal and regulatory documents in support of IND and NDA submissions..Senior Clinical Research AssociateClinical Research Associate IIClinical Research Associate IAlcon Laboratories, Inc.Ft. Worth, TX.Scientist, Pharmaceutical DevelopmentAlcon Laboratories, Inc.Ft. Worth,

Offers a wide range of flexible services to match your needs in biostatistical design and analysis, medical writing, data management, clinical operations, centralised databases, interactive voice resp
Since 1991 Hematologist Consultant at Antoine Beclere Hospital and Beaujon Hospital. He also used to be Senior Resident, assistant to Prof. Pierre Boivin (Beaujon Hospital University Paris VII). Dr. Herrera has published and lectured extensively as an invited speaker at national and international meetings on cancers. He has authored numerous manuscripts in addition to contributing to numerous review articles and book chapters. He is an active member of ASCO (American Society of Clinical

One of the largest CRO's, offering full range of R&D services for pharmaceutical, animal health, chemical, and agrochemical products.
Assist us in helping you find the information you need, please provide us with details of the problem in the text box below. We will investigate and correct the problem as soon as possible. Thank you, Charles River Laboratories Back to top of page.We are dedicated to improving the functionality of our site. To assist us in helping you find the information you need, please provide us with details of the problem in the text box below. We will investigate and correct the problem as soon as

Specializing in national and international Phase I-IV clinical studies. KAI supports web based clinical trials, automated patient diaries, product information centers and provides statistical analysis
KAI Research, Inc. An Exceptional Contract Research Organization.KAI Research, Inc. 11300 Rockville Pike, Suite 500 Rockville, MD 20852-4801.KAI Research, Inc.KAI Research, Inc. An Exceptional Contract Research Organization.Selma C. Kunitz, Ph.D. Founder and Senior Research Scientist.Rene Kozloff, Ph.D, R.N. Founder and Senior Research Scientist.KAI Research, Inc.

A global contract research organization, offering a complete spectrum of services in drug discovery and development.
The Biopharmaceutical Development group provides consulting expertise relating to the scientific and regulatory aspects of the development of biopharmaceutical products. Our team has extensive experience from having worked in both regulatory agency and industry positions with a wide variety of products, to include innovative therapeutic proteins, therapeutic vaccines, monoclonal antibodies, somatic cell therapies, tissue-engineered products, and biological generics. In terms of top ten

Offering services in planning, implementing, and managing healthcare research projects. Based in Alexandria, Virginia, USA.

Provides regulatory and monitoring services for clinical trials, as well as data and project management. Features careers information and company profile. Houston, Texas, USA.

Provides comprehensive Phase I-IV clinical trials support in oncology (cancer), AIDS, infectious disease, and other complex, chronic disorders.

Provides a full range of services specializing in project management, monitoring, data management and statistical analysis serving the pharmaceutical, biotech, and medical device industries.
Moncoa Medical Research Inc. 1125 Howe Street Suite 900 Vancouver, B.C. Canada V6Z 2K8.The site map below shows the pages available on the Moncoa website. You may use the links below, or the navigation bar above to browse throughout the site..

Uses Internet technology to link independent monitors directly with interested pharmaceutical, biotechnology companies and CROs.
Thank you for your interest in subscribing to the newsletter. Monitorforhire registrants automatically receive a copy of the newsletter. If you& ,re not registered, sign up today!.All Rights Reserved. U.S. Patent No. 7,647,240..

A mid-size full-service CRO committed to establishing long-term and successful partnerships with their clients. Experienced in trials for therapeutic and diagnostic products.
Investigation, the Journal of Experimental Medicine, Science, Nature, the Journal of Immunology, and the Annals of Internal Medicine. He is certified by the American Board of Internal Medicine, was elected as a Fellow of the American College of Physicians and of the Infectious Diseases Society of America. He is a past President of the American Clinical and Climatological Association. He has been elected to Phi Beta Kappa and Alpha Omega Alpha. He is the recipient of the Sandoz Award for Medical

Provides quantitative anatomical measurements of brain regions using magnetic resonance imaging (MRI) for neuroscience research, drug trials, and clinical medicine.

An independent research facility which specializes in Phase I and Phase II clinical pharmaceutical studies.
We will investigate and correct the problem as soon as possible. Thank you, Charles River Laboratories Back to top of page.We are dedicated to improving the functionality of our site. To assist us in helping you find the information you need, please provide us with details of the problem in the text box below. We will investigate and correct the problem as soon as possible. Thank you, Charles River Laboratories Back to top of page.

Full service CRO providing clinical research, technical writing, and expert medical advice to the pharmaceutical, medical device, nutraceutical, and related industries.
Offered by SQA in April 2007..William Y.W. Au, M.D. (View CV PDF) Medical Director Clinical Pharmacology and Clinical Research Professor of Medicine, Division of Clinical Pharmacology and General Medicine, SUNY Upstate Medical University, Syracuse, N.Y. Dr Au is a specialist in clinical pharmacology and medical monitoring, endocrinology, metabolism and internal medicine. He has 21 years experience in the pharmaceutical and medical device industry. In addition he has 29 years in academia in

Offers phase I confinement study services to generic, pharmaceutical and biotechnology industries. Located in Pittsburgh, Pennsylvania and Houston, Texas.
Facilities with a total of550 beds in three USA locations. Novum is the second largest CRO in the USA as, measured in bed capacity. Novum averages over 200 Phase I studies performed annually. Novum maintains a highly-experienced management team and staff with the capabilities to perform a wide range of Phase I clinical trials. Although most Phase I studies are conducted with oral dosage formulations, Novum has developed expertise in performing studies with non-traditional delivery systems such

Providing complete worldwide contract research services for phase I through IV clinical trials and pharmaceutics services, including formulation development, stability and analytical chemistry.
King of Prussia, PA 31 January 2011 Omnicare Clinical Research is pleased to announce that Michael Burton, Director, eClinical Solutions will present at the 3rd Annual Clinical Trial Investigator Portals meeting to be held in Philadelphia, PA on 20 May. His presentation is entitled From eLearning Management System to Investigator Portal 2.0 and will take place at 9 00 a.m..

Provides research support services, including project management, temporary resourcing and other project based services to the pharmaceutical industry within North American and/or Europe.
Industry. We specialize in customizing our services to your exact needs.Operatrixoffers a wide variety of specialized research support services, including.We can handle the one-offs .or the management of full-time projects. We can also help you by working with a new team or a new Project Leader at the beginning of a project, helping to plan and strategize, ensuring the team and the project get off to an optimal start..

A group of clinical research sites across the eastern United States. Includes membership information and list of sponsors. Wisconsin Rapids, Wisconsin.

Offers product development, including clinical testing, laboratory services, biostatistical analysis, regulatory services, clinical trial and data management. Wilmington, North Carolina, United States
Trial product development and life cycle management to maximize clients& , investments. Therapeutic leadership for more than 20 years. Contact us to learn more..2011 Pharmaceutical Product Development, Inc. All rights reserved..Proven global CRO leader with more than 11,000 professionals and offices in 44 countries offering clinical trial solutions. Strong track record of partnering with pharmaceutical, biotechnology and medical device companies. Expertise in clinical trial product development

Provides global clinical development services. Through Internet-based technology, PharmaLinkFHI provides pharmaceutical and biotechnology companies real-time clinical development solutions.
Transparent, collaborative and proactive approach to clinical trial management allows our clients to move products to market faster and into the hands of people who need them. Interested in learning more about what Novella Clinical can do for you? Contact us..2011 Novella Clinical. All Rights Reserved.303.4966 European Operations Richmond House, Walkern Road, Stevenage, Hertfordshire SG1 3QP Phone +44 (0)1438 221122.Novella Clinical is a full service clinical research organization dedicated to

San Diego based company provides pharmaceutical chemistry services ranging from methods development and stability testing, to formulation development and small-scale manufacturing for clinical studies
Laboratories, Inc., located at 7330 Carroll Road, Suite 200, San Diego, California 92121..There are no confirmed seminars scheduled at this time. Please check back soon for updates, or sign up for the PTEK U mailing list to be notified about future seminars..Pharmatek Laboratories, Inc. ------------------------------------------------------------------.There are no confirmed seminars scheduled at this time. Please check back soon for updates, or sign up for the PTEK U mailing list to be notified

A focused group of clinical trials professionals with services from Phase 1 and 2 planning, clinical trials, and data management/statistics.

Clinical trials multi therapy site management organization.
Clinical Research Professional.Kishin M. Gehi, M.D. Board Certified Nuclear Medicine, Family Practice.Vipul T. Amin, M.D. Pankaj K. Kashyap, M.D. Board Certified Internal Medicine, Gastroenterology.Rohit G. Patel, M.D. Board Certified Internal Medicine, Pulmonology, Critical Care Sleep Medicine.Chandra K. Gehi, M.D. Board Certified Neurology Sleep Medicine.Rohit G. Patel, M.D. Board Certified Internal Medicine, Pulmonology, Critical Care Sleep Medicine Chandra K. Gehi, M.D. Board Certified

Clinical CRO offering product development, trial and drug safety management. Includes information on services, company background, careers and locations. [Nasdaq: PRAI]
Scientific Affairs combines in-house scientific expertise with hands-on pharmaceutical industry experience. PRA provides clients with therapeutic advice, support, and leadership in translational medicine. Scientific Affairs& , services include.PRA Clinical Operations Group provides clients with highly-trained, locally-based, study teams globally. Our local project teams develop rapport with study sites, ensuring quality and on-time receipt of all clinical deliverables. PRA Lead Clinical Research

Offers design, management and reporting of clinical trials on behalf of pharmaceutical and biotechnology companies. Focus is on the fields of oncology, paediatrics, and anti-infectives.
Ronald Kershner, Ph.D. Named Vice President, Biostatistics and Data Operations at Premier Research Group.Ronald Kershner, Ph.D. Named Vice President, Biostatistics and Data Operations at Premier Research Group.

CRO offering product testing, bioanalytical data analysis and chemical analysis in Whitesboro, New York.

A contract research company providing a widerange of clinical research services for biotech and pharmaceutical clients all over the world.
April 14, 2011 - Quintiles will contribute .6 million over four years to support I-SPY 2, a unique adaptive clinical trial designed to develop breast cancer therapies twice as quickly and at one-fifth the cost of current methods. Read more.March 28, 2011 Quintiles announced that its online social community at www.MediGuard has reached 2.5 million members in just three years. Read more.You are looking for ways not just to survive but to thrive in these challenging times. We help to transform

Provides clinical research services to the pharmaceutical, biotech, device, CRO and SMO industries, and to clinical research investigators.

A Canadian contract research organization (CRO) with a long standing track-record and well established SOP's supporting: protocol development, study design, clinical data management, monitoring, bio-s
Comply with regulatory agency guidelines (ICH, TPD, FDA). SAE Management, ISS Databases and Reports Develop and maintain your product safety database integrated across all clinical studies for the preparation of various regulatory safety updates, ISS report and supporting your product development decisions..

A full-service clinical development organization providing a comprehensive menu of clinical research services to pharmaceutical and biotechnology companies, including clinical operations management, d
For more than 30 years, Premier Research has been conducting clinical research studies to evaluate investigational medication in a variety of medical conditions including acute and chronic pain. We have treated more than 90,000 study volunteers in over 350 clinical research studies. More recently, we have expanded our expertise to include the conduct of clinical studies on healthy volunteers. Our surgeons and physicians are experts in their fields, are board-certified, and have their own private

Conducting clinical research and providing drug development services for the pharmaceutical and biotechnology industries.

National site management organization for phase II-IV clinical investigations for the pharmaceutical, biotechnology, and medical device industries.
In the all or none philosophy. You are always free to select only those sites that you want to use. All sites must (and do) demonstrate their own merit for selection and do not expect to be chosen just because they are part of the network. Budgetary and contractual discussions are always centralized, thus minimizing lengthy negotiations for each site. Please contact us to discuss how we may be able to assist you with your project Richard Turner, President SMO-USA, Inc. P.O. Box 1327 Big Timber,

A full service CRO providing clinical research support to the pharmaceutical, biotechnology and medical device industries.

A full-service CRO offering a complete spectrum of product development, clinical research, and regulatory services.
2009, Symbion Research International, Inc. All Rights Reserved.2009, Symbion Research International, Inc. All Rights Reserved.2009, Symbion Research International, Inc. All Rights Reserved.2009, Symbion Research International, Inc. All Rights Reserved.2009, Symbion Research International, Inc. All Rights Reserved.

A full-service CRO, with expertise in all areas of clinical research, including clinical trial management, data management, regulatory affairs, and biostatistics.
Every stage of your product lifecycle presents opportunities to impact performance. So consider our fundamental proposition Better people, better data, and better processes bring better results..

A provider of clinical research services assisting firms in the clinical trials process from patient enrollments to FDA submission.
And some as voluntary. If you do not provide the mandatory data with respect to a particular activity, you will not be able to engage in that activity. Non-Personally Identifiable Information This refers to information that does not by itself identify a specific individual. We gather certain information about you based upon where you visit on our site in several ways. This information is compiled and analyzed on both a personal and an aggregated basis. This information may include the Web site&

Covering all aspects of regulatory affairs, clinical research, biostatistics, data management, strategic planning, and drug & device development, with specialized advisors in toxicology, analytica
Target e*CRF is a web-based, proprietary, data and project management system designed for ease of use and high throughput. Target e*CRF has been used exclusively by Target Health Inc. since 1999. It is 100% accepted by sites and has been used as the source CRF. As a full service CRO representing over 30 companies at the FDA, we understand what it takes to run a trial. Target Health developed this software to streamline the process and optimize results.Target Health Inc. All Rights Reserved..

A drug development service provider, offering a full range of capabilities, from proof of concept through early stage clinical trials.
Your purpose and personality. Friends, family, customers - anyone in the world with Internet access - can type your domain name into their Web browser and visit your Web site..

Clinical research company in the U.S. serving cosmetic, OTC drug and pharmaceutical clients, providing full-service clinical testing, clinical trials.
May include sensitive categories of information, such as information that reveals racial or ethnic origin, political opinions, religious beliefs, trade union membership, health conditions, or sexual orientation (sensitive personal data).This policy applies to The TKL Research Corporation and its subsidiaries, and is effective as of August 28, 2008. All employees are required to abide by this policy.This policy is designed to protect personal data under applicable law as it is currently exists.

Site management organization located in Canada offering accelerated recruitment and trial management support services
Responsible for the company new business development as well as contributing to the day-to-day operational aspects of the organization and helping to define TMG strategic direction. Prior to TMG, Shawn worked as a principal consultant for the pharmaceutical practice of PriceWaterhouseCoopers (since acquired by IBM Consulting). In that role, Shawn successfully worked with multinational pharmaceutical companies to improve processes and help formulate strategic decisions. He also has experience as

A comprehensive testing laboratory for the biotechnology, biopharmaceutical, medical device, integrated health care, pharmaceutical, and chemical germicide industries.

Offers CRAs and Senior CRAs to provide clinical trial monitoring services on a contract basis throughout the country.
.INFO, .NET or .ORG Annual discounts available on NEW purchases only. GoDaddy is the world& ,s No. 1 ICANN-accredited domain name registrar for .COM, .NET, .ORG, .INFO, .BIZ and .US domain extensions. Source RegistrarSTATS.GoDaddy is rated the world& ,s largest hostname provider according to Netcraft. All rights reserved.

A Washington, D.C. based Contract Research Organization (CRO) offering in vivo preclinicals and research, quality control, and regulatory services for United States FDA submissions.
Electro-Nucleonics Pharmacia Diagnostics included Director of Product Development, Director of Manufacturing and Research Development, and General Manager of Immunodiagnostics. Dr. O& ,Neill led the development and licensing of major diagnostic tests for AIDS and hepatitis and has over 100 publications in enzyme catalysis, immunology and immunodiagnostics.., 1999. All Rights Reserved. Built by Biz-Zone., 1999. All Rights Reserved. Built by Biz-Zone.Le Bars D, Gozariu M and Cadden SW (2001).

A management consulting firm supporting early clinical development of drugs, biologicals and devices.
Петербург, считают эксперты.

Provides GLP services and products that deliver information recommended by the US Food & Drug Administration to predict inter-individual variation in safety and drug efficacy, and to explain adver
. Accordingly, it contains a wide variety of Phase1 and Phase2 enzymes including P450 enzymes, flavin-monooxygenases, carboxylesterases, epoxide hydrolase, UDP-glucuronosyltransferases, sulfotransferases, methyltransferases, acetyltransferases, glutathione S-transferases and other drug-metabolizing enzymes.Liver cytosol contains many xenobiotic metabolizing enzymes including carboxylesterases, soluble epoxide hydrolases, alcohol dehydrogenases, aldehydes oxidases, xanthine oxidases, diamine

Provides clinical research services to the pharmaceutical, biotech, device, CRO and SMO industries, and to clinical research investigators.

Provides clinical research management for the healthcare industry. See lists of services, locations, and upcoming trade shows.

A contract research organization providing analytical services to pharmaceutical companies.
ABC Laboratories& , Chemical Services Division Regulatory Support Endocrine Disrupter Screening Program (EDSP). Tier 1 Screening Battery (T1S) consists of a series of studies designed to detect chemicals that can interfere with hormone systems. The screening battery, which includes ecotoxicity tests with fish and amphibians, is due to be implemented shortly by the US EPA under authority granted by the Federal Food, Drug, and Cosmetic Act. Environmental Assessments for Pharmaceuticals. U.S. Food

Full-service, therapeutically-focused CRO conducting phase I-IV trials for the pharmaceutical and biotechnology industries.

A progressive Clinical Trials Management Organization committed to providing superior service and quality data collection to the medical community.
All Rights Reserved.ACR Idaho2950 E. Magic View Dr. Suite 182Boise, Idaho 83642Phone 208-377-8653.Please see our Current and Future Studies section if you want to learn more about the types of studies we conduct and recruit patients for. In addition, you can fill out the registration form below to be contacted by one of our dedicated patient recruiters for further information regarding the therapeutic areas of your choosing..All Rights Reserved.

Group of scientific and medical professionals providing clinical research services to pharmaceutical and biotechnology industries.
.We ll take you beyond bioequivalence and right through your regulatory submission. At Cetero, we specialize in early phase, and that means.Simple. Complex. For pharmaceutical, biopharmaceutical and generics. Across a wide range of indications. With healthy participants and hard-to-find patients. Plus bioanalytical and scientific affairs experience to get your new medicine off to a great start..

Full-service contract research organization offering regulatory, clinical, reimbursement and compliance services to the medical device and biologic industries.
The device industry. Our people typically have worked in three or more medical device firms, and have supported many others during their career with Alquest. We re of the size where every client matters, yet large enough to offer considerable depth and breadth of expertise. Alquest involvement is determined by your need..Alquest& ,s first client in 1993 was a manufacturer of a neuromodulation device. Since then, Alquest staff members have accumulated significant experience across a variety of

Offers a full array of services to the pharmaceutical, biotech, medical device and medical diagnostic development industries. Services include phase I through IV development planning, protocol develo
Amarex is a full service Contract Research Organization (CRO) that provides clinical regulatory strategy and product development services for drug, medical device and diagnostic kit approvals in the U.S. and other countries..Amarex clients come from around the world and range from small start-up companies to some of the world largest Pharmaceutical firms. The majority of Amarex clients are small and mid-sized companies, and all are treated with equal respect and attention..Amarex offers more

Strategic planning, clinical trial design and management, monitoring, and regulatory affairs services for emerging technologies in the drug, biopharmaceutical, and medical device industry.
And ICH guidelines. We are also well versed in International Regulations, and are prepared to assist with global product development as necessary. Our project Management and monitoring staff members are highly trained and certified. We also provide excellence in Medical Writing, Protocol Development, and preparation of other documents..FDA approval is as dependent on the quality of data as it is on results. Arkios delivers quality, clean data through a formal process according to

A specialty CRO focusing exclusively in monitoring clinical trials. Provides project teams as well as individual monitors for client directed projects.

A nationally recognized leader in clinical trial patient recruitment. We provide complete, creative marketing communications solutions for the healthcare medical marketplace.
Incomplete information we receive is promptly deleted. Important information about the clinical study (contained in what is known as an informed consent form) is reviewed with each patient during the enrollment process by a study professional at the study site. Each patient must read and sign this written information describing the study before enrolling. The written information describes possible health risks and possible benefits of participating in the study, as well as what personally

Delivering independent, scientific support to the pharmaceutical, chemical, agrochemical, food, drink, nutraceutical, consumer healthcare industries and government in assessing the health effects of d
Services include nightly backups, regular maintenance checks and the installation of updates and plugins as and when they become available, so there are no hidden costs throughout the year. For further details please Contact Us.

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