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:
Overview of the content and impact of the new EMA and FDA guidance on computerised systems and electronic data in clinical trials.
Thursday 15 June 2023, 1pm BST (UK), 2pm (CEST, Copenhagen), 8am EST (Boston). Expected duration 90 mins with additional time for your questions.Delivered by GCP and regulation specialists Prof Dr David Hutchinson and Dr Colin Wilsher, with expert data management input from Mr Mark Elsley.
This event is not to be missed for anyone who undertakes clinical trials utilizing computerised systems, electronic clinical outcome assessments eCOA), interactive response technology (IRT), electronic case report forms (eCRFs), electronic informed consent, electronic signatures, artificial intelligence or uses clinical systems.The EMA guideline replaces the important 2010 reflection paper on e-source data and comes into effect on 7 September 2023. Compliance will be critical to avoid findings during inspections.This webinar will focus on the EMA guideline and its impact on the principles, key concepts and requirements relating to the use of computerised systems and electronic data collection in clinical trials.The guideline raises some new requirements as well as reinforcing existing requirements. Where appropriate we will highlight the differences brought about by the FDA’s draft new Q&A guidance on Electronic Systems, Electronic Records, and Electronic Signatures in Clinical Investigations.

Individual connections (single participant): £200
Single connection with up to 5 people taking part – note one connection only): £350
Single connection with 5+ people taking part – note one connection only): £500
Special rates available for organisations needing multiple connections - please contact us for details

Virtual Introduction to Clinical Research & GCP
This course will be delivered in two x 2-hour webinars.
Ideal for those new to clinical research, the non-technical and those in supporting roles and departments, interns, study nurses and administrators, and anyone needing basic training.
We assume no prior knowledge and explain everything. The course will consist of presentations, poll questions, interactive tasks and discussion, and followed by an online quiz.
Group Rates available - contact us for details

The EU Clinical Trial Regulation Virtual Course
Day 1 overviews the current status and summarizes the content of the CTR.
Day 2 looks at the guidelines, related Regulations, CTIS, Q&A document and implementation considerations.
This virtual course consists of two 2-hour webinars.
It will be interactive and involve presentations, workbook tasks, discussion, poll questions and participants Q&A.

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:

Overview and impact of ICH E8(R1) on clinical trials
How to avoid Trial Master File-related inspection findings - TMF guidance explained
Getting to grips with serious breach reporting: a new CTR requirement
Patent Involvement........ making it happen
The Nuts and Bolts of a remote Inspection
Update in Clinical Research & GCP
Reference Safety Information – how to avoid problems
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

Normal webinar pricing:

Individual connections (single participant): £100
Single connection with up to 5 people taking part – note one connection only): £250
Single connection with 5+ people taking part – note one connection only): £400
Special rates available for organisations needing multiple connections - please contact us for details

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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Overview of the content and impact of the new EMA and FDA guidance on computerised systems and electronic data in clinical trials.

Overview of the content and impact of the new EMA and FDA guidance on computerised systems and elect..

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Webinars