Legal Basics for Clinical Study Contracts
European Centre for Clinical Research Training (ECCRT)
Archive
09.10.2014 Brussels, Belgium
Course Content
This course is designed to provide you with an insight in the management of study contracts, the basis of legal requirements for studies and the structure and obligatory items in study contracts. You will receive hints and tricks on understanding and negotiating specific study contract provisions.
This course is designed to provide you with an insight in the management of study contracts, the basis of legal requirements for studies and the structure and obligatory items in study contracts. You will receive hints and tricks on understanding and negotiating specific study contract provisions.
Learning objectives, training objectives
Basic understanding of the legal requirements of a Study Contract
Application of “Good Contract Practice” on Study Contracts
Understanding and negotiating of complex and specific Study Contract provisions
Basic understanding of the legal requirements of a Study Contract
Application of “Good Contract Practice” on Study Contracts
Understanding and negotiating of complex and specific Study Contract provisions
Target Audience
Project Managers (PMs) and upper management; Procurement officers
Project Managers (PMs) and upper management; Procurement officers
Certifications
ISO 9001:2008 / Q-for
ISO 9001:2008 / Q-for
Enquiries and Registration:
Ms. Sunita Kelecom
Clinical Research
Duration
1 day
1 day
Languages
English
English
Fees
EUR 1.000,00
EUR 1.000,00
Organizer contact info
Marcel Broodthaers plein 8b5
1060 Brussels
Belgium
Marcel Broodthaers plein 8b5
1060 Brussels
Belgium
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