Medical Device Regulation 2020 MasterClass

Medical Device Regulation 2020 MasterClass is organized by Global Leading Conferences (GLC) Europe and will be held from Feb 13 - 14, 2020 at Novotel Budapest Danube, Budapest, Hungary.

Who should attend:
This course is designed for executive and operational managers of pharmaceutical companies, especially from packaging operations, as well as IT, artwork operators and engineering staff, responsible for the implementation or operation of the new system. Suppliers of packaging and authentication technology and pharmaceutical packaging companies are also welcome.

What are the impacts on packaging and labelling:
The training course will support you in collecting, sorting and proper understanding of the requirements of the serialisation Requirements in Russia, in Europe, the US and other markets and the Medical Device Regulation. This includes the relevant information related to the Russian Crypto Coding, the defined two EU-safety features (unique identifier and tamper evident closure) and the US and International serialisation requirements. Also, this course will deal with the existing and emerging global serialization and track and trace requirements for medicines and their packaging in markets such as China, Korea, US and others. This course will also deal with Artwork Security and Audit Trails of Artworks Management.

Learning Outcomes:
Serialisation in Russia, the EU and other markets
The requirements for Serialisation in Russia, the EU and other markets
Serialisations Effects
The Serialisations effects and consequences
The Medical Device Regulation
The Medical Device Regulation and its effects
Unique Device Identification
The requirements for Unique Device Identification
Artwork Management
Learn more about Artwork Management
Digital Content Management
Gain insight into Digital Content Management

Additional details will be posted as soon as information is available.