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Regulatory & Industry Liaison

Regulatory & Industry Liaison

Charge

To develop and maintain relationships with industry members and with world regulatory agencies to address issues related to cartilage repair

Responsibilities

Devise and disseminate an ICRS consensus opinion on regulatory matters confronting World Regulatory agencies regarding Cell therapies and scaffold Technology. Develop and maintain relationships with Regulatory bodies such as the FDA , EMEA, AMA and other world regulatory bodies. Host and develop joint meetings including regulators, industry representatives, scientists and physicians for the purpose of maintaining lines of communication and fostering better understanding between the various stakeholders. Develop and maintain relationships with Industry members and aide Scientific Program Committee and Executive Director in fostering sponsorship opportunities for the Society and its Scientific Program meeting

Election and Term of Appointment

Its members and Chair shall be elected and serve as delineated in Election Procedures.

Members

This committee consists of at least 5 members, including the Chairperson. The total membership number is dependent on the working needs of the committee. At least one member will be an Industry representative ad at least one other member should be a Non-physician, Scientist member.

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