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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 Webinars:
Reference Safety Information – how to avoid problems
Wednesday 10 March 2021 @ 1 pm GMT (UK), 2pm CET (Copenhagen) 8am EST(Boston) lasting approx. 90 mins


Webinar cost is based on number of connections, given below in GBP ex VAT

  • Individual connections (single participant): £75
  • Single connection with up to 5 people taking part – note one connection only): £150
  • Single connection with 5+ people taking part – note one connection only): £300
  • Special rates available for organisations needing multiple connections - please contact us for details

 

Virtual Introduction to Clinical Research& GCP
March 27-28, 2021 @ 3pm – 5 pm GMT (UK), 4 pm – 6 pm CET (Copenhagen), 10am-12pm EST (Boston), 7am-9am PCT (SanDiego).

Early bird Price £375 +VAT if booked before 28th February 2021, normal price of £425+VAT thereafter
Group rates available - contact us for details


Comments from our last course …

"I really enjoyed it! David & Colin were really charismatic and interesting to listen to. As a complete novice, it was the right amount of information spoken in the right way.”

“It was one of the most interesting, good, useful and nice trainings which I ever had!”

“Great course, excellent speakers, I enjoyed it, Thank you very much!”

“Excellent.  Will be recommending to colleagues for sure!  a great wealth of information and resources with context to bring it all together.”

A virtual course delivered as two x 2-hour webinars with workbook and fun interactive tasks looking at the basics of drug development, clinical trial terminology and methodology, GCP, participant protection, data collection and management, IMP, safety reporting and Trial Master Files.

No previous experience necessary … all is explained! Ideal for new staff, those needing a basic introduction to clinical research and GCP.

Normal webinar cost is based on connections, given below in GBP ex VAT:

  • Individual connections (single participant): £75
  • Single connection with up to 5 people taking part – note one connection only): £150
  • Single connection with 5+ people taking part – note one connection only): £300
  • 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:

  • Real World Studies.... an insiders guide
  • ICH GCP is changing!
  • ​Practical Advice on how to handle data colection and management in the global pandemic
  • Does your Trial Master File meet the key requirements?
  • Inspection Findings: know what they are and how to avoid common issues
  • 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

I did very much enjoy the webinar, thank you. It gave good thoughts, also on how to move forward and be prepared if another pandemic or similar will hit again. - NBT

Thank you so much for a great presentation - FCDA

The webinar was very good; I enjoyed it a lot - PM

Information was very relevant and definitely lessons to take back to my organisation. Presentation also very professional and audiovisual was excellent - Y Z

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Reference Safety Information – how to avoid problems
Reference Safety Information – how to avoid problems             ..
£75.00
Virtual Introduction to Clinical Research & GCP
Virtual “Introduction to Clinical Research & GCP"             ..
£375.00
Based on 6 reviews.
ICH GCP is changing!
Webinar Recording - ICH GCP is changing!               ..
£50.00
Based on 8 reviews.
Practical advice on how to handle data collection and management in the global pandemic
Webinar recording -  Practical advice on how to handle data collection and management in t..
£75.00
Based on 3 reviews.
Real World Studies ... an insiders guide
Webinar Recording -  Real World Studies ... an insiders guide        &..
£75.00
Does your Trial Master File meet the key requirements?
Recorded Webinar - Does your Trial Master File meet the key requirements?   A reco..
£50.00
Based on 17 reviews.
Inspection Findings: know what they are and how to avoid common issues
Recorded Webinar - Inspection Findings: know what they are and how to avoid common issues - an overv..
£50.00
Based on 7 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.
Current Data Integrity Challenges in Clinical Trials
Recorded Webinar - Data Integrity Challenges A recording of the webinar held live on 13 May 2..
£50.00
Based on 10 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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