Friday, February 24, 2017 —
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?
- European Pharmacopoeia
- Definition of medical grade
MEETING DATE, TIME & VENUE
Wednesday & Thursday, 28 - 29 June 2017
We are looking forward to welcoming you to our joint event!
About MedPharmPlast Europe
MedPharmPlast Europe is a sector group of EuPC created in 2014 by and for companies involved in the whole supply 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. MedPharmPlast Europe also represents the interests of the industry to the European legislators and tries to arrive at regulations that are both workable and protect the patient.
About Toxikon Europe
Toxikon Europe, an FDA registered and ISO 17025 accredited CRO, contracts and partners with Pharmaceutical, Biotech and Medical Device industries to deliver worldwide analytical and microbiological compliances and release testing.
Toxikon has great expertise in:
- Extractables and Leachables testing
- (Bio)Pharmaceutical services
- Microbiology services
- Medical Devices testing
It provides services with state-of-the-art equipment and the technical expertise of its people to generate timely reports with high quality data.