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BW1 - Overview and implementation of the EU Clinical Trial Regulation 2014/536

BW1 - Overview and implementation of the EU Clinical Trial Regulation 2014/536
Product Code: Overview and implementation of the EU Clinical Trial Regulation
Price: £200.00

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PLEASE NOTE: If you are booking for more than one attendee or on behalf of someone else within your organisation you will be required to complete a 'Course Registration' form which can be downloaded by clicking here. Please ensure you click the 'Send to Brookwood Academy by E-mail' button at the bottom left of the form once completed. Failing to complete the form will cause delays in processing your order

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BW1- Webinar
Overview and implementation of the EU Clinical Trial Regulation 2014/536

Monday September 2, 2019, 13.30 CET, 12.30 BST, 08.30 EST
Monday October 28, 2019, 10.00 EST, 15.00 BST, 16.00 CET

•         A 45 minute presentation followed by Q&A.
•         Overview of the new electronic one stop shop to obtain trial authorisation in the EEA.
•         New aspects to obtaining consent.
•         New requirements for trial conduct and notification.
•         Impact for sponsors and investigators.

Single connection for a  maximum 5 of participants:   £200
Single connection for a group of 6+ to unlimited participation using same connection (eg. meeting room with webinar beamed to group):   £400

Discounts are available if multiple connections are required for the webinar, ie if participants need to connect from multiple sites – contact us for details

Webinar packages rates:
Book two webinars, 10 percent discount on total
Book three webinars, 12 percent discount on total
Book four or more webinars, 15 percent discount on total
Book all eight webinars, 20 percent discount on total

Other webinars available are:

BW2 - GDPR – an executive summary or clinical research and pharmacovigilance professionals
Tuesday September 3, 2019, 13.30 CET, 12.30 BST, 08.30 EST
Wednesday  October 30, 2019, 10.00 EST, 15.00 BST, 16.00 CET

BW3 - The interplay between the Clinical Trials Regulation, Clinical Trial Directive and the General Data Protection Regulation
Wednesday September 4, 2019, 13.30 CET, 12.30 BST, 08.30 EST
Thursday October 31, 2019, 10.00 EST, 15.00 BST, 16.00 CET

BW4 - Key factors to make your Trial Master File inspection friendly – an overview of the final EMA TMF guideline
Thursday September 5, 2019, 13.30 CET, 12.30 BST, 08.30 EST
Friday November 1, 2019, 10.00 EST, 15.00 BST, 16.00 CET

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