A two-day course that will ensure you to comply with new regulatory requirements

Clinical Quality Management Systems

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.

Clinical Trial Regulatory 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.

Data Integrity and Document Management

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

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

Managing Vendor/CRO/CMO Oversight

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

Risk Management for Clinical Research

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

The New Clinical Trial Regulation: Overview and Impact

23-24 Apr 2020

Also on: 19 Oct 2020