Common use of Pharmacovigilance Agreement Clause in Contracts

Pharmacovigilance Agreement. As soon as reasonably practicable, the Parties shall enter into a separate agreement providing for the exchange and reporting of Pharmacovigilance Data related to the Product according to industry standards and applicable law.

Pharmacovigilance Agreement. As soon The Parties mutually agree to execute a separate Pharmacovigilance Agreement as reasonably practicable, deemed applicable by the Parties shall enter into a separate agreement providing specifying the procedures and timeframes for the exchange and compliance with Applicable Law pertaining to safety reporting of Pharmacovigilance Data each Product and Licensed Product and their related to the Product according to industry standards and applicable lawactivities.

Pharmacovigilance Agreement. As soon as reasonably practicable, the The Parties shall enter into a separate pharmacovigilance or safety data exchange agreement providing in a form that is customary in the pharmaceutical industry (“Pharmacovigilance Agreement”) reasonably in advance of Innate taking full responsibility for any Commercialization or Development activity with respect to the Licensed Product, outlining their respective responsibilities with respect to the exchange of safety information and the performance of pharmacovigilance activities for the exchange and reporting of Pharmacovigilance Data related to the Licensed Product according to industry standards and applicable lawin accordance with clause 12.4.4.

Pharmacovigilance Agreement. As soon as reasonably practicableIf, at any time during the Agreement Term, the Parties shall agree that it is necessary to enter into a separate pharmacovigilance agreement providing for in order to fulfill their respective local and international regulatory reporting obligations to Regulatory Authorities and other Applicable Law, then the exchange Parties will negotiate in good faith a pharmacovigilance agreement which is consistent with such reporting obligations and reporting of Pharmacovigilance Data related to the Product according to industry standards and applicable lawsuch other Applicable Law.