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
CPE Credit Courses
Enhance your expertise and stay ahead in the biotech industry with our accredited courses designed for professionals like you.
On-Demand Microcourses
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 Microcourses
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 Microcourses
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 Microcourses
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 Microcourses
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 Microcourses
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 Microcourses
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
On-Demand Microcourses
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