All-Access Subscription Bundle

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

85 minutes

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

50 minutes

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

40 minutes

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

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

65 minutes

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

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

8 Hours

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

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

55 minutes

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

55 minutes

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

45 minutes

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

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

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

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

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

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

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

8 Hours

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

4 Hours

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

45 minutes

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

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

8 Hours

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

7 Hours

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

4.5 Hours

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

50 minutes

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

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

50 minutes

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

50 minutes

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

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

60 minutes

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

45 minutes

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

41 minutes

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

41 minutes

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

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

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

57 minutes

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

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

10 Hours