Data Integrity

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.

Introduction to Management of Controlled Drugs, This course covers legislative requirements & GDP guidance in relation to managing and handling Controlled Drugs (CDs) in a wholesale and supply environment. Learn of your obligations and responsibilities as a licence holder and to help you prepare common deficiencies from inspections are also covered.

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.