- Présentations
- Documents
- Infographies
Drug receptors in pharmacology
Bindu Pulugurtha
•
il y a 12 ans
Impurities in Drug Substance & in Drug Product
Kamal Ambalia
•
il y a 10 ans
Dissolution-method Development-PPT
Bhanu Prakash N
•
il y a 8 ans
EU Clinical Trials Regulation.. Summarised
Manish Kainth B.Sc. (Eng), MCIM
•
il y a 11 ans
US and EU Submission – Comparative
Girish Swami
•
il y a 11 ans
C5 eCTD Summit: Electronic submissions and the new Variations Regulation
seront
•
il y a 13 ans
FDA PRO Guidance
Chris Teel Hall
•
il y a 12 ans
Dossier Management and Regulatory Affairs.
Naila Kanwal
•
il y a 8 ans
General dossier requirements for OTC medicines
TGA Australia
•
il y a 9 ans
Comparative Study of Dossier Compilation & Submission Process of Drug Product in USA, Europe & India.
DeveshDRA
•
il y a 12 ans
Common technical document (CTD – ICH)
Mosub Al-Dirdiry
•
il y a 7 ans
Common Technical Document : A Regulatory Document
Turacoz Skill Development Program
•
il y a 7 ans
Introduction to ctd (common technical document)
Ayesha Khursheed
•
il y a 7 ans
Pharmacovigilance
Dr Sukanta sen
•
il y a 8 ans
Common Technical Document
Dr Sukanta sen
•
il y a 10 ans
Marketing Authorization In The Eu
clarityeye
•
il y a 14 ans
USFDA NDA Vs BLA
Girish Swami
•
il y a 10 ans
eCTD Submissions of 2253's
Pyxa Solutions, LLC
•
il y a 7 ans
The Electronic Regulatory Submission
Dr.RAJEEV KASHYAP
•
il y a 14 ans
eCTD in Australia and Experience in the Pilot Programme
TGA Australia
•
il y a 8 ans