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Irb Research

Center for Clinical Research Practice - ccrp.com Aggregated information-based resources for clinical trials aimed at practitioners, sponsors, and foundations. Affiliated with the Thomson publishing firm hippa privacy rule sop standard operating procedures foundations of clinical research irb neirb clinical research clinical education clinical training clinical ethical review   CenterWatch: Clinical Trials Listing Service - centerwatch.com Listing of clinical research trials, information about physicians and medical centers performing clinical research and drug therapies newly approved by the FDA centerwatch jobwatch cwprofessional-com new medical therapies clinical studies clinical research clinical trials clinical testing drug testing fda approvals drug pipeline disease drug therapies medical health patients fda clinicaltrials clinicalstudies illness   Clinimetrics - clinimetrics.com An international company providing consultation and management services to the pharmaceutical, biotechnology and medical device industries. Includes company news, careers information and details of global network. San Jose, California, USA clinimetrics research associates cra cro clinical research associate clinical research organization clinical research assistant trial management project site monitoring protocol development case report form design site selection training data statistical analysis data statistical processing report writing compliance auditing audit sponsor site irb institutional review board   Global Regulatory - globalregulatory.com Pharmaceutical, medical device, biotechnology, food, and nutraceutical consulting for the international markets qa quality assurance gmp audits gmp auditing glp audits glp auditing gmp training glp training fda usfda health canada cro irb pharmaceutical consultants biotech consultants part 11 electronic signatures process validation regulatory consultants medical device consultants food consultants   Institutional Review Board Software from ProIRB Plus, Inc. - proirb.com MS Access Software application designed to assist with compliance and to increase productivity in the IRB administration process. From initial submission, record Study data, meeting agenda preparation, renewals, adverse events, revisions, consent form checklist, IND, and Medwatch numbers, IRB action letters, and letter followup through audit trail reporting irb irb software clinical trial software clinical computer applications drug trial compliance institutional review board irb workflow fda compliance software pharmaceutical development clinical trials regulatory affairs fda hpb standards cro gmp glp administration tracking research institutional review board   RegSource, Inc. - regsource.com Has regulatory affairs data, related federal register notices and links to clinical trials. Regulations and guidelines to NDA, ICH and GCP compliances offered cder cber cdrh cfr fda ind nda irb generic drugs pharmaceutical otc over-the-counter clinical investigator clinical trial gmp good manufacturing practice glp goodlaboratory practice gcp good clinical practice drug approval   Stephens & Associates - stephens-associates.com Offers clinical tests for assessing the safety and efficacy of products, research guidance tests, consumer use studies, microbiological tests, and in vitro tests including non-animal alternative procedures clinical trials cro contract research organization contract clinical research clinical research clinical research management clinical research development global research organization in vitro in vitro manufacture in vitro supplies drug studies institutional review board irb expert reports regualtory consultants scientific writing medical devices personal products prescription drugs data management

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