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DUBLIN – ( WIRE ) – The "EU
Pharmaceutical Regulation and Strategy " conference
was added to the tender of ResearchAndMarkets.com .
This course will provide an up-to-date overview of European politics
regulatory environment, procedures and pharmaceutical obligations.
It will be particularly useful as an introductory or refresher course
for those involved in regulatory affairs or who interact with regulations
staff to understand deadlines and requests for information.
Benefits of Participating
– Understanding the Legal Basis of the EU Regulatory Environment
– Discuss development strategies and pre-submission activities
– Review procedures to apply for marketing authorization in the EU
– Discuss strategic considerations and post-authorization obligations
Why Should You Attend
You will learn the legal basis of regulation, development
strategies and the strategic importance of pre-submission actions, the
format for the presentation of data, how do the registration procedures work?
and post-authorization strategies and obligations.
It will be useful for regulatory affairs staff and also for those
who interact with the regulatory staff to understand the action
deadlines and information requirements.
Who should attend:
This course is for you, especially if it is involved in:
– Regulatory Affairs
– Project Management
– Business Planning
– Commercial Directors
– Manufacturing and quality badurance
– Labeling and Illustrations
– Medical Information
– Clinic
– Pharmacovigilance
For more information on this conference, visit https://www.researchandmarkets.com/research/sx8t8g/eu_pharmaceutical?w=4
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