Develop and advise on regulatory strategies to guide biotech, pharma, and/or device companies through development decisions.
October 03, 2022
Contributes to preparation of high-quality regulatory submissions by helping to organize cross-functional activities pertaining to the regulatory function, including the development of meeting requests, timelines, and compilation of briefing documents intended for submission to regulatory authorities.
December 31, 2022
Support clinical, managerial and executive staff, in developing and/or refining systems that support compliance with standards of accrediting bodies, as well as applicable regulation.
March 09, 2023
Participate in solution development that enable adoption of digital capabilities for Life Sciences organizations.
March 30, 2023
Demonstrate the application of clear, accurate and current understanding of Joint Commission requirements, as well as applicable state, local and federal requirements to allow accurate and timely identification of problem areas.
April 24, 2023
Understanding and showing respect and appreciation for the uniqueness of all individuals.
May 13, 2023