A two-day course that will ensure you to comply with new regulatory requirements
14-15 Nov 2019
Also on: 18 May 2020
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.
30-31 Jan 2020
Also on: 6 Jul 2020
Data Integrity is a critical issue in document governance. It increasingly becoming a focus for regulatory inspections globally. This course will equip you with knowledge necessary to identify and avoid potential Data Integrity issues before auditors do.
5 Mar 2020
Also on: 5 Oct 2020
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
27 Mar 2020
Also on: 25 Sep 2020
This one hour webinar will help you understand what has the impact of GDPR 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
27-28 Apr 2020
Also on: 8 Oct 2020
Ensure your clinical trials comply with the latest focus on GCP inspections and develop your own quality risk management principles and procedures
23-24 Mar 2020
Also on: 28 Sep 2020
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
23-24 Apr 2020
Also on: 19 Oct 2020