Pharmers Academy

27/09/2026

Regulatory Affairs Series:
Day 22
T for Timelines and skills
Everything in Regulatory Affairs is rime sensitive and so should you be too.

25/09/2026

Regulatory Affairs Series:
Day 21
S - Scientif integrity
All drugs which have claims need to have corresponding science (evidence-based therapy). Anything else is guess work.

25/09/2026

23/09/2026

Regulatory Affairs Series:
Day 19

R - Risk

Risk in Regulatory Affairs has potentially devastating consequences. For this reason, it's important to look out for it before hand.
Doing a risk assessment can help your manufacturing company avoid many risks.

series

21/09/2026

Regulatory Affairs Series:
Day 17
P - Post Market Activities are a huge part of health product lifecycle.
Can you name 5 of these activities?

21/09/2026

Regulatory Affairs Series:
Day 16
O - overstate RA Responsibilities
When your CV reads as retail, hospital or anything other than Regulatory, you will 100% not be the preference candidate.

Customize your cv to the role at hand and even with no prior experience, pull out your Regulatory responsibilities from elsewhere.

18/09/2026

Regulatory Affairs Series:
Day 15
N - NCEs

These are originators that are being developed, compiled, registered, marketed and surveilled in a country or region.

16/09/2026

Day 12
L - for Labels
What does it take?
What's the big deal?
Why does the SAHPRA fuss about your label?

15/09/2026

Regulatory Affairs Series:
Day 11
K - Knowledge Management

To be efficient in a sector that's very expensive, uou have to be knowledgeable and manage information well.

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