SFL Regulatory Training Courses on Medtech and on Combination Products
These two training courses provide a comprehensive overview of the EU Medical Device and Combination Products regulations. They can be booked separately, or together.
As part of our holistic approach, SFL provides also specialized training courses where participants can benefit from our team’s cross-functional expertise and learn about the basis and latest developments in Regulatory Affairs, Public Affairs, Legal Services and Medical Communications.
Our training courses have been approved by the SwAPP (Swiss Association of Pharmaceutical Professionals) Commission for Professional Development and SGPM (Swiss Society of Pharmaceutical Medicine). All participants will receive credits upon completion of the SFL training course.
Training Course 1:
EU Medical Device Requirements and Major Changes Ahead
23 April 2013
This course provides an in-depth overview of the EU medical device regulatory framework. As well as learning how to comply with current requirements, attendees will gain insight into forthcoming changes.
Training Course 2:
Regulation of Drug/Device Combination Products, Borderline Products and Companion Diagnostics – Status and Changes Ahead
24 April 2013
This course provides insight into how drug/device combination products and companion diagnostics are regulated in the EU and the US. Attendees will also learn how to prepare for likely upcoming changes to EU device regulations impacting combination products.
(Courtesy of Basel, Switzerland, via switzerland-trips.com)
SFL Regulatory Training Courses on Medtech and on Combination Products
Tue, Apr 23, 2013 - Wed, Apr 24, 2013
SFL Regulatory Affairs & Scientific Communication
Hochstrasse 51, Basel, Switzerland
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