Introduction to Management of Controlled Drugs

This online Data Integrity course is aimed at new starters and existing staff as part of their ongoing Data Integrity training. This course provides a practical overview of the challenges and potential areas of non-compliance that are inherit within paper-based, electronic and hybrid data systems.

In this course you will learn the importance of the requirements of Good Distribution Practice and the EU GDP Guidelines 2013/ C 343/01. Above all, you will know how to implement, and maintain, quality and compliance with GDP guidelines within your company.

Discover the elements and requirements of Auditing. This course focuses on the critical elements of the auditing process for global pharmaceutical distributors, and highlights what can be done to prepare for an audit, and how to address concerns identified following an audit.

Outsourced Activities and Responsibilities of the Licence Holder and Responsible Person, Working both as a refresher and as part of your initial training towards qualification for the position of Licence Holder (LH), or Responsible Person (RP), this course focuses on your duties and responsibilities in respect of outsourced activities, and how to ensure GDP compliance throughout.

This online course was created to provide you with information and guidance into post–Brexit legislation and requirements for importing medicines from a European Economic Area (EEA) State (which is on an approved country for import list) and acting as a Responsible Person for import.