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How to Triage Your Deal Flow: Key Answers You Need
Tuesday, October 28, 2014 and 1:00 pm EST
Sponsored by: Avalere

An early read on the magnitude of risk is essential for effectively triaging deal flow. Join Avalere and industry experts as we discuss two of the most significant questions that companies face when making an acquisition: will the acquired product navigate the regulatory system, and, if so, will it be reimbursed.

Automated Corporate Governance and Compliant Collaboration with Digital Signatures

OnDemand Webcast
Recorded: July 16, 2014
Sponsored by: CoSign by ARX

Get an inside look at the ways global life sciences leaders are applying digital signatures in order to cut costs, enhance collaboration, eliminate non-compliance risks and more. You’ll hear from Rodd Schlerf, FDA Markets Manager at ARX, who has assisted hundreds of life sciences organizations in deploying digital signatures and achieving these benefits and others.


Top 10 Ways to Ensure Your eClinical Technology Meets FDA Guidelines

OnDemand Webcast
Recorded: October 24, 2013
Sponsored by: BioClinica

The best eClinical Solutions should not only streamline the clinical trial process, they should also foster compliance with the FDA and shepherd your data through regulatory submission. This webcast presents guidelines regulating the electronic collection of clinical trial data and shares 10 specific ways to ensure your EDC solution meets the necessary requirements for FDA submission.

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