Live Webinar: How to fast-track becoming serialization compliant in the face of short timelines and complex implementation steps
Falsified medicines have always been a major concern for the European Union (EU) as they represent a serious threat to public health and safety.
Manufacturers, wholesalers, and contract manufacturing organizations (CMOs) will soon have the obligation to guarantee the authenticity of any prescription drugs by identifying individual packs and checking whether the outer packaging of medicines has been tampered with. The delegated EU Falsified Medicines Directive (FMD) will apply as of February 9, 2019.
This webinar will present quick ways to implement these features and comply with the safety and serialisation regulations that will soon be enforced. These preconfigured solutions were specifically designed for those who haven't yet started their serialisation project or are finding themselves behind schedule.
Benefits of attending this webinar
Product Line Manager
Yanik Beaulieu has been with Optel for a total of 8 years, holding various positions in project management, PMO supervision, solution design and, more recently, product line management. Through this valuable experience, he has gained in-depth knowledge of the pharmaceutical industry and customer needs, as his roles have combined the technical aspect, implementation, as well as the business aspect, allowing him to provide excellent insight into the serialization process. Yanik Beaulieu holds a college diploma in Electrical Engineering Technology as well as PMP certification.
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