New Microsoft Word Document
Drug Regulation History Present Future
Gcp 2013
Instructional Design: A Forgotten Art?
ICH GCP
ICH 20 Anniversary Value Benefits of ICH for Regulators
Structure of Dossier of Medicinal Product- Q part Gabriel K. Kaddu Head, Drug Assessment and Registration National Drug Authority Training workshop: Training.
Slide 1 of 72D.K. Mubangizi, Dar Es Salaam Sept. 2007 Training Workshop for Evaluators from National Medicines Regulatory Authorities in East African Community.
General Overview to the CTD and Module 1 Gudrun Dora Gisladottir Director Regulatory Affairs.
Reference documentation and drugs production according GMP. Material balance. Lecture 1.
What is ICH? ICH is a joint initiative involving both regulators and research-based industry representatives of the EU, Japan and the US in scientific.
What is ICH?