A two-day course that will ensure you comply with new regulatory requirements.
19-20 Nov 2020
Also on: 17 May 2021
This course will take you through the key regulatory and guideline requirements for clinical research in Europe, including the new EU Clinical Trial Regulation and existing Directive requirements.
28-29 Jan 2021
Also on: 5 Jul 2021
Data integrity is a critical issue in document governance and is increasingly becoming a focus for regulatory inspections globally. This course will equip you with the necessary knowledge to identify and avoid potential data integrity issues before auditors do.
5 Oct 2020
Also on: 5 Mar 2021
This course will provide an essential understanding to help with compliance with the new regulation and associated implementing acts and other texts for carrying out clinical trials in the EU
19-20 Oct 2020
Also on: 22 Apr 2021
This course provides an update on recent changes to ICH GCP R2, EU Clinical Trial Regulation and guidance and will discuss how these changes have been implemented
25 Sep 2020
Also on: 23 Mar 2021
This one-hour webinar will help you understand what the impact of GDPR has been on drug development
25 February 2019 – 2pm (GMT)
We can customise this course to meet your requirements.
Learn how to prepare a Request for Proposal (RFP), evaluate and select the right CRO and establish procedures for vendor oversight for R&D projects you need to outsource
8-9 Oct 2020
Also on: 26 Apr 2021
This must-attend new event will provide an essential overview of the opportunities and challenges presented by orphan drug regulation.
23 Sep 2020
Also on: 10 Mar 2021
Ensure your clinical trials comply with the latest focus on GCP inspections and develop your own quality risk management principles and procedures
28 Sep 2020
Also on: 22 Mar 2021