BIO Professional Development

Through a curated network of education alliance partners, BIO offers industry professionals executive training and development resources for accelerating career growth

Featured Courses
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OSHA Bloodborne Pathogens Regulations details current OSHA Bloodborne Pathogen Regulations, how to determine if your organization is subject to its laws, and how to properly integrate them into existing medical surveillance, health, and safety programs.

Professional Certificate
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What are considered good publication practices for communicating company-sponsored medical research and how do these practices impact publication development and planning?  Learn more in this pub planning module.

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Take your next step to ensure that the field of digital health is worthy of our trust.

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A good regulatory strategy is essential to a good business strategy.

Professional Certificate
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Diagnostic Development and Approval describes the regulatory pathways for different categories of diagnostics, emphasizing the differences between in vitro diagnostics and laboratory-developed tests. Quality system regulations are extensively reviewed. The course ends with a discussion on the economic evaluation of novel diagnostics. Diagnostic Development and Approval helps anyone in the diagnostics industry expand their diagnostics development acumen.

Professional Certificate
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Diagnostics' Role in Medicine Today introduces the ever-expanding molecular diagnostics industry. Diagnostics save lives by helping to pinpoint the exact cause and location of disease. Learn the purpose of each type of diagnostic, the science behind personalized medicine, and how companion diagnostics help doctors prescribe medication and dosage correctly the first time. If you are new to this area of health care, Diagnostics’ Role in Medicine Today will provide a solid foundation on which to build your diagnostic acumen.

Professional Certificate
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Learn how to bring a drug successfully to market.

Professional Certificate
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Do you need to understand the drug development process, including details about a drug's life cycle from its discovery through post-marketing studies?  This is the course for you.

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Drug Discovery of Biologics explains the steps involved in discovering new biologics, with a special...

Professional Certificate
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Explains the steps involved in discovering, validating and optimizing new therapeutics.

Professional Certificate
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Elements of a Biorisk Management Program summarizes the major practices and principles, as well as the tools necessary, for organizations to integrate biological safety and biorisk management techniques into their existing laboratory operations and programs.

Professional Certificate
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Explore life sciences/healthcare innovation from the vantage point of the world’s most successful startup ecosystem – Silicon Valley.

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A digital strategy can no longer lie within a siloed digital or innovation team. It’s critical to integrate digital across the enterprise to maintain a competitive edge.

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Comprehensive review of the Do's and Don'ts for AD/Promo Tactics: covers types of drug and medical device advertising, promotional labeling (booklets, brochures, direct mail, exhibit booths, file cards, monographs, publications, sales aids, videos).

Professional Certificate
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Detailed review of content do's and don'ts including comparative/superiority, charts/graphs, competitor information, “cherry-picking”, disclaimers, references, market research data, quality-of life claims, company spokespeople. 

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Do we correct information about our drug in a company’s sponsored chat room? What types of websites shouldn’t we link to? Learn the FDA regs and more.

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Do we correct information about our drug in a company’s sponsored chat room? What types of websites shouldn’t we link to? Learn the FDA regs and more.

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How do you “frame” risk information for a prescription product?  What are misleading ‘signals’ in audio or visual promotion? Learn the FDA regs and more?

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What are the requirements for posting on Twitter?  What happens if you decide to  correct misinformation on the Internet? Learn the FDA regs and more.

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How should reprints with off-label information be issued once they have appeared in peer-reviewed medical journals? Learn the FDA regs and more?

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What are the three basic requirements for press releases?  How do you know whether a press release  is fairly balanced?    Learn the FDA regs and more.

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What are the FDA requirements for prescription drug advertising versus promotional labeling? Can secondary endpoints be used in product promotion? Learn the FDA regs and more.

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Do we correct information about our drug in a company’s sponsored chat room? What types of websites shouldn’t we link to? Learn the FDA regs and more.

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What are the members of the promotional review team and why are these functional roles important for Medical, Legal and Regulatory (MLR) Review? Learn about MLR and more.