GLP vs GMP vs GCP Dominique Pifat, Ph.D., MBA The Biologics Consulting Group [email protected] Common Misconception Good Laboratory Practices 1) A quality system concerned…
Overall CDM Process ICRI Introduction CDM is consistently being recognized as a primary part of clinical development team & in some instances leads this team! Evolution…
1. Presented byPaul Below, CCRA, CCRT P. Below Consulting, Inc. Conducting Studies to theInternational Gold StandardGoing Beyond What the FDA Requires 2. Learning Objectives•…
1. BY SAIDULU& SHIVA DEEPTHI CLINCAL PHARMACOLOGY DEPARTMENT 2. Requirements and guidelines for permission to import and/ or manufacture of new drugs for sale or to undertake…
Slide 1Study Design Jason Rock [email protected] 215-253-7474 [email protected] Slide 2 Table of Contents Goals of the Study Design Message Scope of work…
Slide 1Essential Documentation GCP Training Seminar 12 th October 2011 Anne Thomas Sister, Dermatology Clinical Research Cardiff University Slide 2 Introduction Essential…
Slide 1Food and Drug Administration Center for Biologics Evaluation and Research The Office of Cellular, Tissue, and Gene Therapies Web Seminar Series presents: The Office…
1.Protocol FIL_PTCL13 V. 1.0 18 Nov. 2013 Page 1/60STUDY PROTOCOLROMIDEPSIN IN COMBINATION WITH CHOEP AS FIRST LINE TREATMENT BEFORE HEMATOPOIETIC STEM CELL TRANSPLANTATION…
Electronic Health Records for Clinical Research GLOBAL SHARING FOR GLOBAL HEALTH: TRUSTWORTHY REUSE OF HEALTH DATA Digital Health Assembly, Cardiff Dipak Kalra President…
For more information, please call 855.818.3406 or visit www.impgraphics.com STUDY MATERIALS FULFILLMENT LOGISTICS an Imper ia l Company CASE STUDY GOAL Develop a comprehensive…