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DESCRIPTION:Are you up to date with the regulatory requirements for clinic
 al research?\n\nDo you understand the impact and new requirements of the 
 EU Clinical Trial Regulation?\n\nThis course will take you through the ke
 y regulatory and guideline requirements for clinical research in Europe\,
  including the new EU Clinical Trial Regulation and existing Directive re
 quirements. Key US requirements which impact on trials being carried out 
 in Europe will also be briefly covered.\n\nThe interactive programme will
  highlight the most important of these key requirements and changes and h
 ow these are likely to impact on trials now and in the future for pharmac
 eutical and biotechnology companies and study sites.\n\nKey topics to be 
 covered include:\n\n\nThe current requirements of the EU Clinical Trials 
 Directive\nThe EU Clinical Trial Regulation (536/2014)\nThe impact of Bre
 xit\nClinical trial authorisations\nComplexities for running paediatric t
 rials\nRequirements for managing investigational medicinal products\nLega
 l aspects of clinical trials\nRequirements of pharmacovigilance\nICH upda
 te\nRegulatory inspections\n
DTEND:20210129T163000
DTSTAMP:20260512T213552Z
DTSTART:20210128T093000
LOCATION:\,
SEQUENCE:0
SUMMARY:Are you up to date with the regulatory requirements for clinical r
 esearch?\nDo you understand the impact and new requirements of the EU Cli
 nical Tr...
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