The importance of inspection readiness for your organization and clinical trial


In the last couple of years, regulatory authorities worldwide have been placing more emphasis on the inspection of how computerized systems are used in clinical trials. The regulatory authorities expect you to be able to present and explain relevant documentation about those systems on demand.

By attending you will learn:

  • Why inspection readiness is important for your organization and your trial * How to become inspection ready
  • About the advantages of using Viedoc to prepare for inspection

Discover how others have prepared for regulatory inspection and how you, too, can be fully prepared for your next inspection. Sign up now.

Meet the speakers

Mark Williams
Vice President
WCG-ACI Clinical

Mark brings the customer perspective to the webinar. He will be speaking of the pitfalls to avoid and regulatory requirements to meet when preparing for inspection.

Alan Yeomans
Quality Manager
Viedoc Technologies

Alan has years of experience within Life Sciences and has worked with Quality and Regulatory Compliance. He will be speaking on how to best prepare for inspection.

Robert McGrath
VP BD North America
Viedoc Technologies

Robert is responsible for Viedoc in North America and has a long history of building strong client relations. He will moderate the webinar.

Sverre Bengtsson
Strategic Relations
Viedoc Technologies

Sverre Bengtsson, as a Co-Founder has a long history within the company building strong client relations. He will introduce Viedoc Technologies and the participants.

Would you like to know more but have a scheduling conflict?

No need to miss out.

Register anyway and you’ll get access to the webcast on-demand following the event.