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On-Demand

CPE Credit Courses

Enhance your expertise and stay ahead in the biotech industry with our accredited courses designed for professionals like you.

On-Demand Micro Classes

Biotech for Non-Scientists

Elevate your communication by acquiring expertise in the foundational science driving the biopharma industry.

The Biology of Biotech

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

85 minutes

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

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

Immunology Primer 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

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

Biosimilars Primer

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

65 minutes

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

Cell Therapy Primer

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

45 minutes

On-Demand Micro Classes

Drug Development for Non-Scientists

Boost your competitive edge by navigating the complex development process and regulatory environment to ensure faster drug approvals.

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

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

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

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

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

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

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

Clinical Development 101: General Principles

Sets the stage for the entire clinical development process. The general principles discussed include who conducts trials and their roles.

55 minutes

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

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

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

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

On-Demand Micro Classes

Drug Manufacturing for Non-Scientists

Enhance your manufacturing expertise by learning the concepts, language, and processes that increase operation efficiency and safety.

Biomanufacturing Primer

Introduces the essentials such as cell lines, cell banks, upstream/downstream bioprocessing, and the latest advancements in this dynamic field. Grab your spot!

50 minutes

Pharmaceutical Manufacturing Primer

Introduces the complex processes of manufacturing, packaging, and transporting small molecule drugs and covers essential aspects of production.

45 minutes

Gene Therapy Manufacturing Primer 101

Ventures into the essential AAV production platforms, comparing four different approaches and dissecting the key elements of the AAV cassette.

50 minutes

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

cGMP Primer

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

50 minutes

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

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

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

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

On-Demand Micro Classes

Medical Device and Diagnostics for Non-Scientists

Increase your fluency in medical device technology and regulations to work more effectively with industry clients, colleagues, and regulators.

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

Diagnostics’ Role In Medicine Today 

Introduces diagnostics used in research and clinical settings, such as immunochemistry, microbiology, and infectious disease. Become diagnostic proficient!

41 minutes

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

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

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

Medical Device Commercialization Primer

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

55 minutes

Medical Device Development Primer

Broadly explores the workflow of the 5 pivotal stages of medical device development, from evaluating market opportunities to scaling manufacturing. Join us!

57 minutes

Medical Device Approval Primer

Identifies the regulatory compliance requirements for different medical device classifications, from Class I to III, that are critical to ensuring patient safety.

55 minutes

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