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 forthcomingWebinar events

Next Webinars:
Contact us now for details of upcoming webinars or if you have any ideas for a webinar subject


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:

  • Focus on the things that matter ... a risk proportionate approach to clinical trial management
  • Key points on the revision of the Declaration of Helsinki, and introducing the Declaration of Taipei
  • Trial Master File Key Requirements and the Essentiality of Documents
  • The Draft E6(R3) Guidance - what's new and Different
  • Overview of the content & impact of the new EMA & FDA guidance on computerised systems and electronic data in clinical trials
  • 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): £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

 

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


Focus on the things that matter … a risk proportionate approach to clinical trial management

Focus on the things that matter … a risk proportionate approach to clinical trial management

Focus on the things that matter … a risk proportionate approach to clinical trial managementA record..

£200.00

Key points on the revision of the Declaration of Helsinki, and introducing the Declaration of Taipei

Key points on the revision of the Declaration of Helsinki, and introducing the Declaration of Taipei

Key points on the revision of the Declaration of Helsinki, and introducing the Declaration of Taip..

£200.00

Trial Master File key requirements and the essentiality of documents

Trial Master File key requirements and the essentiality of documents

Trial Master File key requirements and the essentiality of documents A recording of the webinar..

£200.00

The draft E6(R3) GCP guideline – what’s new and different

The draft E6(R3) GCP guideline – what’s new and different

The draft E6(R3) GCP guideline – what’s new and different  A recording from Wednesday 5 July..

£200.00

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 electronic data in clinical trials.

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

£200.00

Overview and impact of ICH E8(R1) on clinical trials

Overview and impact of ICH E8(R1) on clinical trials

Overview and impact of ICH E8(R1) on clinical trials A recording of the webinar held  on Tuesd..

£75.00

How to avoid Trial Master File-related inspection findings - TMF guidance explained

How to avoid Trial Master File-related inspection findings - TMF guidance explained

How to avoid Trial Master File-related inspection findings - TMF guidance explained Recordin..

£75.00

Getting to grips with serious breach reporting: a new CTR requirement

Getting to grips with serious breach reporting: a new CTR requirement

Getting to grips with serious breach reporting: a new CTR requirement  A recording of the we..

£75.00

Patient involvement … making it happen

Patient involvement … making it happen

Involving patients in clinical trial development Patient involvement … making it happen A record..

£75.00

The Nuts and Bolts of a Remote Inspection - sharing experiences

The Nuts and Bolts of a Remote Inspection - sharing experiences

The Nuts and Bolts of a Remote Inspection - sharing experiences A recording of the webinar held o..

£75.00

Reference Safety Information – how to avoid problems

Reference Safety Information – how to avoid problems

Reference Safety Information – how to avoid problems             ..

£75.00

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