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All-Access Subscription Bundle

Non-CPE

This subscription includes all non-CPE Microcourses and Recorded Signature Courses in the following certificate programs with an additional $400 discount and unlimited access to over one hundred 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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THE BIOLOGY OF BIOTECH

Provides an overview of biotechnology’s most important biological molecules and systems to make novel therapies and diagnostics.

85 minutes

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GENETIC ENGINEERING PRIMER

Defines the process of genetic engineering DNA and its uses. Genetic engineering is the deliberate modification of genetic material (DNA).

50 minutes

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IMMUNOLOGY PRIMER 101

Explains how the human immune system fights infectious diseases and cancer. Learn how pathogens cause disease and distinguish between immune systems.

40 minutes

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IMMUNOLOGY 201

Builds on the Immunology 101 class to describe the two types of immune systems, the nonspecific immune system, and the specific immune system.

55 minutes

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ANTIBODY PRIMER

Examines the versatile role of antibodies, including how they are used in research and the clinic. Increase your fluency in the science of antibodies.

70 minutes

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BIOSIMILARS PRIMER

Explains the science, manufacturing technology, and regulatory requirements for receiving approval to market. Don’t miss out, secure your spot!

65 minutes

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GENE THERAPY PRIMER

Provides a foundational understanding of this versatile therapeutic’s science and regulatory process. Learn how gene therapy works—the type of vectors used.

90 minutes

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CELL THERAPY PRIMER

Offers a comprehensive introduction to cell therapy development, manufacturing, and commercialization. Level up your knowledge!

45 minutes

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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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SMALL MOLECULE DRUG DISCOVERY PRIMER 101

Showcases the essential steps to finding and bringing new compounds to market. Don’t miss this opportunity! Enroll today!

55 minutes

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SMALL MOLECULE DRUG DISCOVERY PRIMER 201

Examines early screening techniques and breaks down lead optimization and drug design methodology and approaches. Grab your seat now!

55 minutes

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DRUG DISCOVERY OF BIOLOGICS PRIMER 101

Showcases the 5-step discovery process, spanning target ID and verification to candidate ID, validation, and optimization. Join us today!

45 minutes

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DRUG DISCOVERY OF BIOLOGICS PRIMER 201

Provides insights into antibody discovery, including the significance of screening, structure-based affinity maturation, and CMC liabilities.

45 minutes

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PRECLINICAL DEVELOPMENT PRIMER 101

Guides you through essential steps of early-stage drug development and efficacy/safety standards that must be met prior to beginning clinical trials.

55 minutes

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PRECLINICAL DEVELOPMENT PRIMER 201

Utilizes real-world examples to delve deep into the specific tests and data required to file a successful IND application. Secure your spot today!

55 minutes

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DRUG APPROVAL PRIMER

Offers a comprehensive overview of how small molecule drugs and biologics receive the regulatory green light for human use. Level up your knowledge!

60 minutes

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CLINICAL DEVELOPMENT 101: GENERAL PRINCIPLES

Builds on the Immunology 101 class to describe the two types of immune systems, the nonspecific immune system, and the specific immune system.

55 minutes

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CLINICAL DEVELOPMENT 201: PHASE I

Explains the purpose of Phase I and the regulatory roles of the FDA, IRB, and EMA. Class highlights include how data from bioequivalence, pharmacokinetics, and pharmacodynamics studies are used.

50 minutes

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CLINICAL DEVELOPMENT 301: PHASE II/III

Expertly explains the purpose and critical differences between well-controlled Phase II and III studies and the art of trial design. Join us!

55 minutes

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CLINICAL DEVELOPMENT 401: PHASE IV

Surveys the ongoing post-approval clinical assessments required by regulatory agencies. Learn how drug risk management is accomplished through detecting, assessing, and reporting.

50 minutes

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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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BIOPHARMA BUSINESS ACUMEN PRIMER

Provides a comprehensive understanding of the business considerations needed to develop and bring a life-saving cure to the marketplace. Join today!

45 minutes

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APPLYING FOR A LIFE SCIENCE JOB PRIMER

Demonstrates the power of a well-crafted resume and cover letter and why both are crucial for landing your dream life science job. Unlock your career potential!

36 minutes

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INTERVIEWING FOR A LIFE SCIENCE JOB PRIMER

Explains how the human immune system fights infectious diseases and cancer. Learn how pathogens cause disease and distinguish between immune systems.

36 minutes

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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

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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

Drug Manufacturing

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cGMP PRIMER

Introduces 6 requirements: QMS, Premises and Equipment, Personnel Training, Materials Management, Documents and Records, Validation and Qualification. Register!

50 minutes

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CMC PRIMER

Provides an overview of CMC across every stage of drug development, from discovery to preclinical and clinical development, ending with post-launch considerations. Gain insights!

45 minutes

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BIOMANUFACTURING PRIMER

Provides an overview of biotechnology’s most important biological molecules and systems to make novel therapies and diagnostics.

50 minutes

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PHARMACEUTICAL MANUFACTURING PRIMER

Defines the process of genetic engineering DNA and its uses. Genetic engineering is the deliberate modification of genetic material (DNA).

45 minutes

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GENE THERAPY MANUFACTURING PRIMER 101

Explains how the human immune system fights infectious diseases and cancer. Learn how pathogens cause disease and distinguish between immune systems.

50 minutes

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GENE THERAPY MANUFACTURING PRIMER 201

Explains the science and regulatory controls of 4 AAV platforms’ features, functions, and design, including TT, rBV/Sf9, HSV/BHK, and PCL. Register!

65 minutes

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LABORATORY WORKER BIOSAFETY PRIMER

Provides an initial framework for the practices and principles laboratory workers should consistently use when working with toxins and infectious biological agents.

60 minutes

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IMPLEMENTING A BIOSAFETY PROGRAM PRIMER

Summarizes the effective practices, principles, and controls used to integrate biological safety and security protocols into existing and new laboratory operations.

40 minutes

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OSHA BLOODBORNE PATHOGEN STANDARD PRIMER

Focuses on preventing the spread of infectious diseases by managing the chain of infection and handling biohazardous materials safely. Enroll today!

45 minutes

Medical Device and Diagnostics

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DIAGNOSTICS’ ROLE IN MEDICINE TODAY

Defines the process of genetic engineering DNA and its uses. Genetic engineering is the deliberate modification of genetic material (DNA).

41 minutes

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DIAGNOSTIC DEVELOPMENT PRIMER

Navigates the regulatory requirements for Class I, II, and III diagnostic approval pathways. Become well-versed in the diagnostic approval process!

41 minutes

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DIAGNOSTIC MEASUREMENTS PRIMER

Surveys the measurements used to assess a diagnostic’s accuracy. A test must achieve a certain level of accuracy before receiving regulatory approval. 

47 minutes

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DNA-BASED DIAGNOSTICS PRIMER

Breaks down the critical technology that drives diagnostic advancements, including PCR, microarrays, NGS, and microRNA diagnostics. Keep pace and enroll today!

44 minutes

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PROTEIN-BASED DIAGNOSTICS PRIMER

Focuses on antibodies: what they are, where they come from, and how they work. Covering sandwich and bead immunoassays, multiplexed assays, lateral flow assays, and chromatography.

40 minutes

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MEDICAL DEVICE DEVELOPMENT PRIMER

Explains how the human immune system fights infectious diseases and cancer. Learn how pathogens cause disease and distinguish between immune systems.

57 minutes

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MEDICAL DEVICE APPROVAL PRIMER

Builds on the Immunology 101 class to describe the two types of immune systems, the nonspecific immune system, and the specific immune system.

55 minutes

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MEDICAL DEVICE COMMERCIALIZATION PRIMER

Reveals best practices for preparations, sales, marketing, and reimbursement, ensuring readiness and effective healthcare promotion. Register now!

55 minutes

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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

Features

  • Closed Captioning in English, Spanish, French, French Canadian, Hindi, Japanese, Korean, Mandarin, Russian, Standard Arabic
  • Transcripts in English, Spanish, French, French Canadian, Hindi, Japanese, Korean, Mandarin, Russian, Standard Arabic
  • Course materials
  • Real-time tracking
  • Progress reporting
  • Accessibility features
  • Corporate account upgrades
  • LinkedIn certificate attachment
  • Verified certificates

Ready to get started?

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