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