COVID Cure LoRes

Solutions to COVID-19 Business Continuity and Fast Track Trial Challenges – Clinical and Regulatory Aspects



Who should watch: Clinical and Regulatory executives affected with business continuity issues and/or are working on COVID-19 trials

Structure: Presentation and Q&A Roundtable – 45 min

What you will learn:

  • Status on COVID-19 guidelines from major health authorities (FDA, EMA, MHRA etc.)
  • Fast track implications for IND and CTA filings to start trials without delay
  • Impact for clinical trials – rapid deployment of teams, accelerated document processing, maintaining required quality
  • Chances and potential of automation tools to reduce trial time
  • Planning ahead for NDA and MAA filings to ensure quality submissions and a speedy start to the review process

Major Webinar Highlights:

  • Presentation of current COVID-19 projects Phlexglobal is working on. Sharing of best practices, key metrics, learnings and results.

Complete this short form to watch the webinar and access the slides.


Karen Roy Circle

Karen Roy
Chief Strategy Officer

Jim Nichols 02

Jim Nichols
Vice President
Product Management,  Business Applications

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