Compliance officer for start-up biologic company

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Reference no: EM133652883

Question

A compliance officer for a start-up biologic company that is planning to launch its first clinical trial. Your colleagues have asked you for your input on drafting and negotiating the clinical trial agreement. They are particularly interested in the sections concerning confidentiality, indemnification, data ownership, intellectual property, and publication. They have asked the compliance officer to review language for these sections from model agreements available online, drawing from these models, The compliance officer must draft a memo that (1) presents at least two different options for each of the sections, and (2) explains the implications of choosing one of the options over the other.

Reference no: EM133652883

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