Objectives

During this conference, speakers from European authorities, industry, sciences and donation service provide you information about the current developments of the regulatory requirements, strategies to accomplish the goal of a European standard. Furthermore, the developments on microbial safety – requirements and methods – will be introduced. With their presentations, these experts will present their practical experiences and knowledge in the field of quality and safety of blood, blood products and plasma.

Information is also given on the contribution of the manufacturing process of plasma derived medicinal products with respect to viral safety and reduction of thrombosis generating agents. For plasma derived final products Directive 2001/83/EC requires an official control authority batch release. This aspect is as well matter of discussion at this conference.

Target Audience

This conference is designed for people from

• Donation services
• Authorities
• Plasma Fractionation
• Control Laboratories

who are involved in regulatory affairs, quality assurance, quality control and manufacturing of blood , blood products or plasma.

Registration

To register for this course please see the Registration Options.