Ways to Manage Clinical Trial Challenges in a Pandemic Period

Ways to Manage Clinical Trial Challenges in a Pandemic Period
Product Code: Ways to Manage Clinical Trial Challenges in a Pandemic Period
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Furter to the very successful webinar please find here links to the presentation and supporting documantation
Webinar notes:

Regulatory documents (as of 12:00 25 March 2020):

You can view again the presentation only by visiting …

Don’t forget our range of online training and new electronic books – you will be amazed! Look at our e-brochure by clicking …

Wednesday 25 March at 2.00pm GMT (3.00pm CET)

Part webinar, part discussion …. Prof Dr David Hutchinson and Dr Colin Wilsher will present relevant guidance and recommendations and will discuss how to deal with the challenges of the current virus pandemic and its impact on clinical trials.

Topics include:

• Risk assessment and mitigations
• Protocol amendment (including urgent safety measures) and violations
• SOP impact
• Consent: including e and remote consent, consent to continue
• Monitoring: alternatives to face to face visits
• Investigator replacement strategy
• Supply of IMP including home delivery
• Documentation of actions
• Rules for suspension and termination (ICH, EU UK Regs)


Please send your questions for discussion in advance, if possible, to

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