Webinar: Responsibilities at GDP

The globalisation of the pharmaceutical supply chain has created new challenges for the manufacture and supply of medicinal products in various markets. Directives, Guides, Guidelines and initiatives from various regulatory bodies lead the way in this development and define expectations and requirements, where Good Manufacturing Practices (GMP) and Good Distribution Practices (GDP) are closely linked. In 2013 the revised new “Guidelines on Good Distribution Practice of Medicinal Products for Human Use” were published. Chapter 2 “Personnel” defines the qualification requirements, tasks and responsibilities of all staff and the Responsible Person (RP).
The requirements to be met include the following:

For our webinars, we use Cisco WebEx, one of the leading suppliers of online meetings. At http://www.webex.com/test-meeting.html you can check if your system meets the necessary requirements for the participation at a WebEx meeting and at the same time install the necessary plug-in. Please just enter your name and email address for the test. If the installation is not possible because of your rights for the computer system, please contact your IT department. WebEx is a standard nowadays and the necessary installation is fast and easy.