Structuring and Reviewing Clinical Research Contracts

Who should attend? This seminar is an excellent overview for those already working with contracts and is specifically designed for R&D, Contracts and Finance Managers. However, if you have limited experience then the practical examples are particularly useful. Other job titles who have also benefited from this valuable day are Senior Research Nurses, Clinical Trial Support Managers, Industry, Business and Legal Service Managers. What you will take away? When you don’t want to make mistakes, this event will lead you through the pragmatic approaches you need to take, isolating common issues and highlighting what you need to look out for. By taking one day out, you will be able to identify key risks and improve your expertise of approving contracts, rather than sending them on for in-house legal review. What are the key learning outcomes? This day will ensure that you fully understand the practical realities of clinical research contracts. • Examine what is included in the clinical research model contract • Unmask essential confidentiality, indemnity and intellectual property issues • Understand the model non-commercial clinical trial agreement and material transfer agreements • Share examples of negotiation, modification and how to avoid classic pitfalls • Insight into foreign sponsors: working with the US and Europe • Details of what key areas Trusts should focus on for non-standard agreements

04 de marzo de 2015 | London (Reino Unido)


Holiday Inn London-Gatwick Airport

Povey Cross Road, Horley, Surrey, RH6 0BA

London (Reino Unido)


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SBK: Leading Events in Healthcare

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