Your Team Uses AI. You're Worried About Your Reputation.
Your team discovered ChatGPT. They're using it for regulatory docs, clinical reports, client deliverables. You're auditing everything because you can't afford AI slop embarrassing you in front of FDA, clients, or investors.
I train biotech teams to create AI-assisted work you can trust - without you auditing every word.
Why biotech teams trust me:
You Can't Audit Everything
Your team is using AI for regulatory docs, clinical reports, and client deliverables. You know it. They know you know it. The problem: you're now spending hours auditing everything because you can't afford AI-generated errors embarrassing you.
That defeats the entire purpose of AI. You didn't approve these tools so you could work more.
You need a team that produces AI-assisted work you can trust—without you auditing every word.
Why Biotech Is Different
Generic AI training teaches "10 ChatGPT prompts" that work fine for marketing emails. Biotech teams need something different:
The Real Cost of AI Slop
When AI-generated work goes wrong in biotech, the consequences aren't just embarrassing—they're expensive:
FDA Rejection
Hallucinated references or inaccurate claims in regulatory submissions
Lost Partnerships
Generic AI output that signals lack of scientific rigor to pharma partners
Failed Grants
Boilerplate language that reviewers immediately recognize as AI-generated
Bad Decisions
AI-summarized data with subtle errors that compound into strategic mistakes
How This Works
This isn't a generic AI course. We work with your actual artifacts and build quality control frameworks specific to your environment.
Understand Your Artifacts
We analyze the specific documents your team produces—regulatory submissions, clinical reports, grant proposals—to identify where AI can help and where it introduces risk.
Identify Quality Risks
We map the failure modes specific to biotech: hallucinated citations, incorrect terminology, regulatory non-compliance, and generic output that undermines credibility.
Build Verification Frameworks
We create quality control checkpoints tailored to your workflow—so your team knows exactly how to verify AI output before it leaves the building.
Train on Real Work
We practice with your actual documents, not generic examples. Your team leaves with workflows they can use Monday morning.
Services
VP Assessment
On-site or virtual assessment for leadership:
- Analyze current AI usage and quality risks across your team
- Identify regulatory and reputational vulnerabilities
- Written recommendations specific to your environment
You leave knowing exactly where AI helps, where it hurts, and what to do next.
Schedule AssessmentTeam Training Program
Two-day intensive using YOUR actual artifacts:
- Work with real regulatory submissions, reports, proposals
- Build quality control frameworks for your specific document types
- Hands-on practice with verification workflows
- 60 days implementation support included
Your team leaves with documented workflows they can use immediately.
Discuss Training ProgramRetained Quality Partnership
AI quality control on retainer:
- Monthly training updates as AI tools evolve
- Unlimited artifact review and quality checks
- On-call support for high-stakes deliverables
For teams with ongoing high-stakes document production.
Discuss PartnershipWho This Is For
If your team's output reaches regulators, clients, or investors, you need quality control for AI-assisted work.
Regulatory Affairs VPs
Submissions that go to FDA, EMA, or other agencies
Clinical Operations VPs
Study reports, protocols, and site communications
R&D Directors
Scientific publications and internal research documents
Medical Affairs Leads
Medical communications and KOL materials
Business Development
Partnership materials and investor presentations
Quality Assurance
SOPs, audit documentation, and compliance records
Why Biotech Teams Trust Me
BS in Biotechnology
I speak your language. I understand GxP, regulatory frameworks, and why "close enough" isn't acceptable in your world.
Published Research
Peer-reviewed research on antibacterial nanostructures. I understand scientific rigor and what it takes to produce work that survives peer review.
200+ Professionals Trained
I know how to teach complex technical concepts to teams in regulated industries. Not theory—practical skills they use the next day.
Ready to trust your team's AI output?
Schedule Confidential AssessmentOr email dydavidyoussef@gmail.com with "Biotech AI Training" in the subject.
What People Say
Feedback from workshop participants and professional connections
"Just had a prompt engineering workshop with David and it was a pretty jam packed one hour. David knows his stuff and has kept up to date with the state of the art. He also shared templates and strategies generously but more importantly sets up the *way* to think about approaching LLM's as well as larger meta questions around breaking down problems. Highly recommend!"
Sagar Dubey
Workshop Participant
"David is an autodidact and an exceptional communicator. He is consistently fascinated by both the sales process as a whole and the details of interpersonal communication and decision making. I highly recommend him for any sales or marketing position."
Michael House
Professional Connection
Technical Background
I build AI systems and tools - the same technical depth I bring to understanding how AI works in practice.
Ready to Trust Your Team's AI Output?
Let's discuss how to build quality control frameworks for your biotech team:
- Quality control frameworks for AI-assisted biotech artifacts
- Training that lets you trust your team's output
- Regulatory-aware AI workflows for your specific documents
Or email me at dydavidyoussef@gmail.com with "Biotech AI Training" in the subject.