Webinars

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