Cro Service Agreement

13.9 Global Agreement. This Agreement constitutes the entire Agreement between the Parties, together with each IPA and the schedules and exhibits annexed thereto, and supersedes all prior or simultaneous agreements, understandings or assurances entered into or between the Parties, in writing or orally, which may affect the subject matter of this Agreement. All amendments or additions to this Agreement (including handwritten amendments) are null and void, except in the case of a written deed signed by authorized representatives of both parties. 8.10 Fight against corruption. CRO complies with all applicable anti-bribery laws and regulations, including, but not limited to, the U.S. Foreign Corrupt Practices Act of 1977, as currently drafted, or the U.K. Bribery Act of 2010, as currently drafted, and shall not cause the Promoter to violate any of the anti-bribery laws and regulations in the countries where the Promoter operates. CRO recognizes the continued desire to provide services to the proponent. and crOs specializing in clinical trials can offer their customers the know-how to bring in a new drug or device, from its design to fda/EMA marketing authorization[4], without the drug sponsor having to have staff for these services. [5] (g) Exclusion. .

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