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Recorded Signature Course Subscription

Non-CPE

This subscription includes all non-CPE Recorded Signature Courses in the following certificate programs at 75% discount with unlimited access to over sixty hours of life science training.

  • Biotech for Non-Scientists
  • Drug Development
  • Business of Biotech
  • Drug Manufacturing
  • Medical Devices and Diagnostics

Biotech for Non-Scientists

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Recorded BioBasics 101: The Biology of Biotech for the Non-Scientist

Offers a fascinating exploration of the foundational scientific principles that underpin the life sciences. Register for our most popular course!

8 Hours

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Recorded BioBasics 201: Targeted Therapeutics Explained for the Non-Scientist

Highlights the pivotal roles, mechanisms of action, and next-gen innovation of vaccines, antibodies, gene and cell therapies, and RNA medicines. Join us!

9 Hours

Drug Development

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Recorded Drug Development Immersion

Explores the commercial, regulatory, and scientific factors that pave the way for a successful drug launch. Register today and increase your drug development acumen!

9 Hours

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Recorded Biopharmaceutical Commercialization Immersion

Explains the strategic aspects of bringing a drug to market and maximizing its commercial potential. Join us and uncover tactics for success!

8 Hours

Business of Biotech

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Recorded Commercialization Readiness From Preclinical to First Launch

Equips early-stage biotechnology leaders with the knowledge they need to make informed strategic choices for long-term success.

4 Hours

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Recorded Revenue Forecasting and Epidemiology Immersion

Showcases the intersection of epidemiology, revenue forecasting, and drug valuation. Grab your seat today!

7 Hours

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Recorded Drug Pricing, Policy, and Utilization Immersion

Exposes complexities of the US healthcare market by detailing how competing forces determine patients’ access, use, and cost of medications. Join!

4.5 Hours

Medical Device and Diagnostics

man taking an online class

Recorded Medical Device Development Immersion

Navigates the changing regulatory environment and pathways devices undertake for FDA or EMA marketing approval. Learn from an industry expert!

10 Hours

Ready to get started?

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