Each module contains topics, knowledge checks, decision-tree scenarios, an interactive quiz, podcast, intro video, and downloadable resources.
The promotional regulation framework — principles, scope, enforcement.
What counts as promotion. High-risk traps from PMCPA rulings.
Hierarchy of evidence, drafting defensible claims, comparative-claim pitfalls.
Sign-off authority, certification, regulatory standing of the signatory.
Detailing aids, off-licence interactions, hospitality boundaries.
Slide decks, reactive content, scientific exchange vs promotion.
Fees, sponsorship, transparency, EFPIA disclosure.
Web, email, social media, AI tools — the new high-risk surface.
MSL boundaries, congress activity, advisory boards.
Brand-neutral campaigns, named-patient access, patient organisations.
SOPs, complaint handling, MHRA inspection readiness.
Live case-rulings drill. Sign-off readiness assessment.
Build sign-off judgement from real PMCPA case rulings. Defensible decisions, fewer cycles, audit-ready.
Scientific exchange vs promotion, congress activity, advisory boards, KOL engagement — without the compliance landmines.
Get fluent in what will and won't pass sign-off — before drafting. Materials approved faster.
“The AQP Path is the programme I wish had existed when I qualified as a Final Signatory. 26 years of pharmaceutical compliance, 1,900+ PMCPA rulings, distilled into 12 weeks of structured progression. Every lesson is one I've learned the hard way — so you don't have to.”
One real case. One key lesson. Every week — free.