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Webinars

We facilitate Webinars on a variety of subjects relating to clinical trials.
​Be sure to bookmark this page and check back frequently to view our forthcoming Webinar events.

Next Webinar:
Inspection Findings: know what they are and how to avoid common issues
- an overview of recently published GCP & PV inspection findings.
Thursday 11 June 2020 2:00 pm BST, 3:00pm CET (Brussels), 9:00 am EST (Boston, USA)
Lasts around 75 mins, with panel discussion and Q&A for as long as participants need.

  • A look at the most recent publications of GCP and PV inspection findings from the USA, Europe and UK.
  • Some inspection do’s and don’ts as described by a regulator!
  • ​Are you ready for remote inspections? - A brief look at the changing face of inspections
  • Certificate of attendance will be provided for each participant.

Webinar costs are based on connections, given below in GBP ex VAT:

  • Individual connections (single participant): £50
  • Single connection with up to 5 people taking part – note one connection only): £100
  • Single connection with 5+ people taking part – note one connection only): £200
  • Special rates available for organisations needing multiple connections - please contact us for details

Webinar Recordings
Missed the Webinar, no worry. You can catch up by viewing the recording. All previous webinars are now available to view on demand. Simply choose the course from the list below or contact us at info@brookwood-global.com for more details. 

Brookwood’s series of past webinars include:

  • Ways to Manage Clinical Trial Challenges in a Pandemic Period
  • Data Integrity Challenges
  • Overview and implementation of the EU Clinical Trial Regulation 2014/536
  • GDPR – an executive summary or clinical research and pharmacovigilance professionals
  • The interplay between the Clinical Trials Regulation, Clinical Trial Directive and the General Data Protection Regulation
  • ​Key factors to make your Trial Master File inspection friendly – an overview of the final EMA TMF guideline

Participants' comments
Many thanks for this webinar: timely, clear and comprehensive. The course handouts are very well presented too.  Also I found it helpful to hear the questions and concerns of others in the call. -SH

The webinar was very informative. I appreciate your organizaton making this available. -FP

Great presentation and Q&A session yesterday. I particularly appreciated the discussion topics as we navigate the unknown together. - SB

 

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Inspection Findings: know what they are and how to avoid common issues
Next Live Webinar to be held live on 11 June 2020 Inspection Findings: know what they are an..
£50.00
Data Integrity Challenges
Recorded Webinar - Data Integrity Challenges A recording of the webinar held live on 13 May 2..
£50.00
Based on 10 reviews.
Ways to Manage Clinical Trial Challenges in a Pandemic Period
Recorded webinar - You can watch this free of charge Ways to Manage Clinical Trial Challenges in a ..
£0.00
Based on 5 reviews.
Overview and implementation of the EU Clinical Trial Regulation 2014/536
Recorded webinar - Overview and implementation of the EU Clinical Trial Regulation 2014/536 A rec..
£50.00
General Data Protection Regulation – an executive summary for clinical research and pharmacovigilance professionals
Recorded webinar - General Data Protection Regulation – an executive summary for clinical research a..
£50.00
The interplay between the EU Clinical Trials Regulation, Clinical Trial Directive and  the General Data Protection Regulation
Recorded webinar - The interplay between the EU Clinical Trials Regulation, Clinical Trial Directive..
£50.00
Key factors to make your Trial Master File inspection friendly – an overview of the final EMA TMF guideline
Recorded webinar - Key factors to make your Trial Master File inspection friendly – an overview of t..
£50.00
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