Fälschungssicherheit in der Pharmaproduktion 2013
June 10 - 12, 2013
Implementation of the Directive in the company Falsified Medicine
The conference bridges the gap from the comparatively basic aspects of international anti-counterfeiting measures to the detailed requirements that shape the daily work: implementation of encoding and serialization of drugs in the company, the tamper
Evident features dos and don'ts during official GMP inspections or the implementation of QRD recommendations to name a few. The dialogue between authorities and relevant institutions and industry will not only uncover any remaining weaknesses, but also to emphasize successes.
The Top 5 of this event
National and international requirements for protection against counterfeiting
Tamper Verification features for pharmaceutical packaging
Serialization in the international environment
Parallel importing in new Serialisierungssystem
Preparing for GMP Inspections
The conference bridges the gap from the comparatively basic aspects of international anti-counterfeiting measures to the detailed requirements that shape the daily work: implementation of encoding and serialization of drugs in the company, the tamper
Evident features dos and don'ts during official GMP inspections or the implementation of QRD recommendations to name a few. The dialogue between authorities and relevant institutions and industry will not only uncover any remaining weaknesses, but also to emphasize successes.
The Top 5 of this event
National and international requirements for protection against counterfeiting
Tamper Verification features for pharmaceutical packaging
Serialization in the international environment
Parallel importing in new Serialisierungssystem
Preparing for GMP Inspections
Venue
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Fälschungssicherheit in der Pharmaproduktion June 10 - 12, 2013
