Browsing Tag
M. Pharm
85 posts
DEVELOPING CLINICAL TRIAL PROTOCOLS, INSTITUTIONAL REVIEW BOARD, INDEPENDENT ETHICS
DEVELOPING CLINICAL TRIAL PROTOCOLS, INSTITUTIONAL REVIEW BOARD, INDEPENDENT ETHICS COMMITTEESubmitted to: Submitted by: PROF. JAVED ALI Saniya Takkar…
INVESTIGATOR BROCHURE PDF/PPT
INVESTIGATOR BROCHURE PRESENTED BY:SADAF SALEEM M.PHARM (PHARMACEUTICS) SEM ISPER,JAMIA HAMDARD CONTENTS Introduction Why are investigator’s…
Investigation of medicinal products dossier(IMPD) PDF/PPT
Investigation of medicinal products dossier(IMPD) Submitted by: Submitted to:SADAF SALEEM DR. SANJULA BABOOTAM.Pharm (Pharmaceutics) Dept. of PharmaceuticsSemester-ISPER, JAMIA…
Drug Approval In United States, Europe, India PDF/PPT
1 Contents: 2 Introduction Drug Approval In United States Drug Approval In Europe …
Dossier, Impd and Ib (PDF/PPT)
Dossier, Impd and Ib Deepak GuptaM.PharmJamia Hamdard 1 Introduction• Dossier is a collection or file of documents…
Regulatory requirements of EU, MHRA,TGA AND ROW COUNTRIES PPT/PDF
Regulatory requirements of EU, MHRA,TGA AND ROW COUNTRIES PRESENTED TO :- DR. SANJULA BABOOTA DR. JAVED ALI PRESENTED…
ICH GUIDELINES M.PHARM (PHARMACEUTICS) PDF / PPT
ICH GUIDELINES PRSENTED BY: SUKHMEET TANGRI M.PHARM (PHARMACEUTICS) MENTORED BY:Dr. JAVED ALI Dr. SANJULA BABOOTA INTRODUCTION The…
E-CTD (ELECTRONIC COMMON PDF / PPT
E-CTD(ELECTRONIC COMMON TECHNICAL DOCUMENT) 1 The ELECTRONIC version of ctd is known as E-Common Technical Document.…
CTD (COMMON TECHNICAL) PDF/PPT
CTD(COMMON TECHNICAL DOCUMENT) Deepak GuptaM.Pharm (pharmaceutics) Jamia hamdard1 CONTENTSo Validationo Submitting the e-CTD • CTD o Benefits…
SCALE UP AND POST APPROVAL PDF/PPT
SCALE UP AND POST APPROVAL CHANGES (SUPAC)Submitted by: Gaurav (M.pharma pharmaceutics) Jamia hamdard Submitted to:- Dr.Sanjula Baboota &…