Everything that lives behind this site, available to download.
The full curriculum in PDF. The one-page summary. The sector point of view. Case studies as they land. Brand assets where procurement needs them. No gates, no forms.
Click and download. The full biopharma curriculum PDF is the most-used resource on this page. Everything else is supporting material.
Title, description, format. Direct request link.
The page is functional. No marketing copy beyond the brief item descriptions. If the item you need is gated by a request, it usually arrives within a working day.
The full biopharma curriculum pending upload
PDF of the canonical curriculum document. Three modules. Twenty sub-modules. Every learning objective. The same content reproduced verbatim across the curriculum pages of this site, packaged as a single shareable document for offline review and internal circulation.
Programme one-page summary pending upload
A single-page leave-behind covering what the programme is, what it produces and where to read more. Designed for forwarding internally to anyone who needs the headline before they invest time in the detail.
Why Embed, Why Now - biopharma point of view in production
Brightbeam's published view on the regulatory and commercial pressure shaping biopharma AI adoption today, and how organisations should respond. Covers the EU AI Act high-risk classification, the build-over-buy economics, the cost of shadow AI and the case against waiting. The full version of the argument summarised on the Why Embed, Why Now page of this site.
Regulatory landscape briefing new for biopharma
A standalone briefing on the regulatory frameworks the curriculum operates inside - EU AI Act, ICH Q-series (Q2/Q3/Q7/Q9/Q10/Q11/Q12), GAMP 5, EU Annex 11, ICH E6 GCP, ICH E2E pharmacovigilance, FDA AI/ML guidance, MHRA software guidance and EMA reflection papers. Refreshed within thirty days of any material change.
Case studies awaiting authorisation
Anonymised case studies of biopharma engagements published as authorisation lands. Currently in preparation. Named-client conversations are available on request through the contact in the footer.
Security and data handling pack supplied on request
The full security and data posture documentation procurement and IT typically request during evaluation. Includes the standard data processing agreement template, security questionnaire pre-answers, IP terms, sub-processor disclosure, cross-border transfer provisions and vendor qualification responses suited to a biopharma Global Tech review.
Brand assets pending upload
Logos and brand reference for procurement and legal teams that need to attach Brightbeam materials to internal documents.
If a resource you need is not listed here, the contact in the footer can usually produce it within a working day. The list above is the standard set; bespoke material is produced on request as part of an active engagement.
Questions about the curriculum belong in FAQ. Questions about the company belong in About Brightbeam.
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