Zielgruppe

• pharmacists and other scientists
• engineers and technicians
• everyone working in: pharmaceutical development, manufacturing,
   regulatory affairs, quality control or business development

Zielsetzung

The workshop is designed for professionals working in the pharmaceutical and medical device industry in the following areas: drug development, medical device development, manufacturing, quality control, quality assurance and regulatory affairs who are actively engaged with the development, manufacture and quality control of drug-device combination products.

This workshop which is organized by APV’s MedTech Task Force addresses the regulatory requirements and technological challenges of drug-device combinations and related primary packaging components both for Europe and North America and goes along practica examples for different routes of administration and manufacturing technologies.

For the first 15 registered participants, a guided tour through a modern manufacturing facility for medical devices (Boehringer Ingelheim microParts, Dortmund) will be provided as additional value based on availability and approval.
Please note that the participation of each person to the facility tour has to be approved by Boehringer Ingelheim micropParts in regards to competitor protection rules. Each approved participant will get a separate confirmation. There is no legal right to participate in the guided tour.