University of Tampa Bay (UTB) — Pharmaceutical Education Reimagined · Est. February 2026
University of Tampa Bay University of Tampa Bay4i · Industry Integrated
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Two days. One certificate.

Three executive crash courses, written out in full and taught inside the UTB learning platform. Every module is transcribed from the course handbook, every knowledge check is marked with its reasoning, and every course ends in an examination that issues a numbered certificate the moment you pass it.

$9Every crash course — one flat $9, one-time. No subscriptions, no hidden fees.

3Certificates
25Modules
305Questions written
115Charts & diagrams
70%Pass mark
MFG-401$9 · One-Time

Pharmaceutical Manufacturing & Industry 4.0

Innovate · Automate · Lead

How a medicine moves from formula to finished product — the workflow, the dosage forms, the departments that own each decision, and the EU GMP backbone underneath all of it. Then what Industry 4.0 actually changes on the factory floor: MES, IIoT, real-time release, and where AI genuinely earns its place.

The six modules

  1. Pharmaceutical Manufacturing Fundamentals
  2. Pharmaceutical Production Operations
  3. Industry 4.0 in Pharmaceuticals
  4. AI & Digital Manufacturing
  5. Quality by Design & Process Excellence
  6. Smart Pharma Factory & Future Careers
ANL-401$9 · One-Time

Advanced Pharmaceutical Analytics & Stability

HPLC · ICH Stability · Data Integrity

The laboratory as a regulated instrument: what HPLC, GC, UV-Vis, FTIR and dissolution each answer, how a method is validated under ICH Q2, how stability is designed under ICH Q1, and what an OOS or OOT result obliges you to do next. Data integrity runs through all of it.

The eight modules

  1. Introduction to Pharmaceutical Analysis
  2. Analytical Instrumentation Overview
  3. Analytical Method Validation (ICH Q2)
  4. Stability Studies (ICH Q1)
  5. Data Integrity & Laboratory Documentation
  6. Out of Specification & Out of Trend
  7. Digital Analytics & AI in the Laboratory
  8. Industry Case Studies & Career Development
REG-401$9 · One-Time

Regulatory Affairs & Global Compliance

US FDA · EMA · MHRA

The longest of the three, and the most procedural: how the FDA, EMA and MHRA differ in practice, what the CTD and eCTD actually require of a submission, how change control and regulatory intelligence keep a licence current, and where the career paths run.

The eleven modules

  1. Introduction to Global Regulatory Affairs
  2. Drug Development Lifecycle
  3. US FDA, EMA & MHRA Regulatory Frameworks
  4. CTD & eCTD Fundamentals
  5. Regulatory Submission Process
  6. Global GMP & Compliance Essentials
  7. Regulatory Documentation & Lifecycle Management
  8. Regulatory Intelligence & Change Control
  9. AI Applications in Regulatory Affairs
  10. Real Industry Case Studies
  11. Career Opportunities in Regulatory Affairs
How a crash course runs

Read it, check yourself, sit the paper.

Step 01

Sign in

One student account opens all three crash courses. No application, no waiting on an admissions decision.

Step 02

Read the modules

The handbook in full, with charts, defined terms, worked scenarios and interview questions. Your place is kept as you scroll.

Step 03

Check yourself

Knowledge checks sit inside each module and are marked with the reasoning, so a dropped mark tells you what to read again.

Step 04

Sit the examination

Twenty questions drawn from every module. Pass at 70% and your certificate is issued immediately — numbered, printable, verifiable.

Your first module is already written.

Sign in with your student account and start reading — the platform remembers where you stopped.

Student Login → Compare with normal courses