25-26/9 - Regulatory Affairs and Good Distribution Practice (GDP)
Tuesday-Wednesday September 25-26th
The Regulatory Affairs function in healthcare- and life science industries is vital in making safe and effective healthcare products available all over the world. The demand for academics in Regulatory Affairs has increased steadily the past 2 years.
This course will enhance your chances in getting positions not only within Regulatory Affairs but also as Medical- Scientific Advisor, Medical Scientific Liaison (MSL) Quality Assurance (QA). You as a delegate will be given a certificate after the course. In addition to this you will have advice on how to best visualize the course in your CV.
Comprehensive training on relevant regulations and guidelines to fully understand the requirements in submitting new Market Authorizations as for Human Medicinal Products in Europe and how to maintain the life cycle management through submitting relevant variations and line extensions; and how to maintain the safety in pre- and post-approval phases, as well as understanding the complexity of working in a matrix organization.
Comprehensive training also on all chapters in the EU-GDP legislation and the practical applications of those, leading to understanding how to gain and maintain a Wholesaler license.
Lecturers with long-term, well-documented and proven excellent track record in the field
To be updated in Regulatory Affairs and GDP-standards and requirements, thereby optimizing your chances in getting positions within the Life Science Industry.
Important information regarding Registration
Send your CV along with a motivation why you should enroll this course to firstname.lastname@example.org prior to registration.
Date and time
Tuesday-Wednesday September 25-26
Day 1 - 9am-4pm
Day 2 - 9am-12am
Kungsgatan 60, Stockholm
Apply at Mina Sidor Kund...
Lecturer Niclas Lindqvist
This course is in English
This course is held at Kungsgatan 60 in Stockholm