Regulatory Affairs in Pharmaceutical Industry
Description
Course Curriculum
Regulatory Affairs in Pharmaceutical Industry
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Part 1 – Introduction
00:31 -
Part 2 – Understanding R.A
01:08 -
Part 3 – Importance of R.A
00:44 -
Part 4 -Regulatory Agencies
01:26 -
Part 5-Public Health as the Paramount Concern
01:17 -
Part 6 – Ensuring Safety and Efficacy of Drugs and Medical Devices
01:05 -
Part 7- Regulatory Affairs Emphasis
01:54 -
Part 8 – New Drug Approval
01:26 -
Part 9 – Abbreviated New Drug Application (ANDA)
00:46 -
Part 10 – Key Components of ANDA
01:30 -
Part 11 – Steps of ANDA
03:36 -
Part 12 – Standardizing Regulations Globally
01:01 -
Part 13 – Challenges in Regulating Innovative Therapies
00:57 -
Part 14 – Career Opportunities in R.A
00:49 -
Part 15 – Educational Qualifications
00:40 -
Part 16 – Essential Skills to Excel in R.A
01:44 -
Part 17 – Role of R.A
01:47 -
Part 18 – Color Coded Regulatory References
02:24 -
Part 19 – Key Takeaways
01:34
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