Global Serialization 3 of 3: A Closer Look at EU Falsified Medicines Directive
(Thu, Dec 3, 2015, 11 am Eastern Time)
EU Falsified Medicines Directive (FMD) became effective in 2013 bringing in all 28 countries under one unified rule of supply chain security. FMD called for the “Delegated Act” to define the technical specifications of serialization and track-n-trace. The draft of the Delegated Act was published in August 2015 spelling out very detailed rules of implementation for the industry. Join this webinar to learn the EU requirement and its deadlines.
- Manufacturers’ requirement
- Wholesale distributors’ requirement
- EU-Hub and Data reporting
- Exceptions handling
- Verifications and reporting