Pharma Packaging Quality Control and Serialization MasterClass - US edition

 This course will deal with Child Resistant packaging, with Smart packaging and will cover tamper evident packaging and the qualification of tamper verification features on healthcare packaging.

26-27 February, 2024, Virtual

Time Zone: Eastern Standard Time (EST) - UTC−05:00

Overview

The training course will support you in collecting, sorting and proper understanding of the requirements of pharma and healthcare packaging. This master class will deal with quality control and quality management requirements and procedures of primary and secondary pharma and healthcare packaging. This course will cover AQL testing in packaging controls and reduced sampling procedures for pharma packaging.

The training course will deal with the global serialization requirements in Europe, in Brazil, in the US and in other markets and the technical implementation at the pharmaceutical manufacturer. The course will cover serialisation and aggregation of medicinal products and will also deal with the implementation of UDI (unique device identification) for medical devices and the medical device regulation in Europe and in the US.
 

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RECOMMENDATION

Who should attend?

This course is designed for executive and operational managers of pharma and healthcare companies and pharmaceutical manufacturers and medical device producers, especially from quality departments and packaging operations, as well as packaging designers, regulatory affairs, IT, artwork operators and engineering staff, responsible for the implementation and the operation of the new systems. Suppliers of packaging materials and manufacturers of pharmaceutical packaging components are also welcome as well as suppliers of authentication technology and services.