Don't miss this opportunity to gain an insight into the most important topics for the medical devices and pharmaceutical packaging industry: Save the Date for the joint event of MedPharmPlast Europe and Toxikon on 28 - 29 June 2017 at Toxikon Europe in Leuven.
What can you expect? Our event will cover among others these topics:
Material Qualification and Characterisation - by Toxikon Europe
Update on Medical Device Regulation
Conformity Assessment - What will change under the new MDR?
Definition of medical grade
MedPharmPlast Europe is a sector group of EuPC created in 2014 by and for companies involved in the complete value chain of plastic medical devices and pharmaceutical packaging in Europe.
It assists companies in these industry sectors by keeping them informed about the latest developments in European regulations and their impact on the medical device and pharmaceutical packaging plastics value chain. As an expert group with other trade bodies, MedPharmPlast Europe furthermore represents the interests of the industry to the European legislators and tries to arrive at regulations that are both workable and protect the patient.
MedPharmPlast Europe believes that this is essential to ensure that patients have access to safe, affordable medical devices and pharmaceutical packaging. That can only be achieved by avoiding increased regulatory complexity and costs that will reduce the competitiveness of the European industry.
MedPharmPlast Europe Communications
MedPharmPlast Europe President
MedPharmPlast Europe Vice President
Regulatory Task Force Chairman
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