Duration: (22:27) ?Subscribe5835 2025-02-14T23:06:33+00:00
Regulatory Submissions and Applications
(2:51)
Preparing for Review: Regulatory Submission
(2:45)
U S FDA Medical Device Pre Market Regulatory Submissions
(14:46)
Role of the Regulatory Affairs in Pharmacovigilance
(16:34)
Short course on the Medical Device Regulation (EU) 2017/745
(14:55)
Electronic Submissions (7of27) Generic Drugs Forum 2018
(18:22)
Regulatory Submission and Documentation: Path, Pitfalls and the Use of AI from May 2024
(22:27)
Regulatory Affairs in Pharmaceutical industry I RA department l Interview questions and answers
(10:49)
Making good clinical trials easier \u0026 more equitable: Updated ICH GCP guidelines
(57:56)
What is Regulatory Affairs Management in Clinical Research?
(5:41)
Vol 24 - Insider Tips for CMC Regulatory Submissions: Avoiding Common Pitfalls
(9:9)
How to Register an Investigational New Drug (IND) to the US FDA
(3:25)
What is Regulatory Affairs? | A PharmD in the Pharmaceutical Industry
(10:19)
EPISODE 9: Providing Regulatory Submissions for Medical Devices in Electronic Format
(16:27)
Regulatory Affairs Explained Episode 1: FDA, Application Types, Regulatory Pathways \u0026 More
(10:24)
Division of Filing Review: Helpful Tips for Submission of an ANDA or Controlled Correspondence
(23:35)
eCTD Submission Challenges
(23:45)
Regulatory Affairs
(1:6:5)
Life of Regulatory Affairs Associate | Clinical Research Institute in India | Clinical Research
(3:33)