Question 1

What is pharma AI literacy?

Accepted Answer

Pharma AI literacy is the skills and judgment to deploy, review, and govern AI in regulated life-sciences work — from understanding model limits and the jagged frontier to applying FDA credibility expectations and EU AI Act Article 4 obligations in GMP settings.

Question 2

Who is the Pharma AI Literacy Center for?

Accepted Answer

Quality, manufacturing, validation, IT, data science, and leadership roles in pharma and biotech — anyone who needs to speak credibly about AI with regulators, auditors, or cross-functional teams in the US and EU.

Question 3

How long does the assessment take?

Accepted Answer

The benchmark assessment has 20 multiple-choice questions across five domains and typically takes about six minutes. You receive instant scoring with domain breakdowns and module recommendations.

Question 4

Does the tool cover FDA and EU requirements?

Accepted Answer

Yes. Five assessment domains and eight learning modules span AI fundamentals, pharma use cases, FDA's risk-based AI credibility framework, and EU AI Act / GMP Annex 22 expectations — with a 71-term glossary aligned to both rulebooks.

Question 5

Is the Pharma AI Literacy Center free?

Accepted Answer

Yes. The assessment, all eight modules, glossary, score readout PDF, and Article 4 completion certificate are free with no login required.

Question 6

Is this legal or regulatory advice?

Accepted Answer

No. Content is educational only. Draft guidance cited (FDA AI credibility; EU GMP Annex 22) should be verified against final texts before use in submissions or audits.