Join Quorum Review at the 2012 PRIM&R Advancing Ethical Research Conference: Guided by Principles in an Era of Change.
The conference brings together 3,000 industry professionals from hospitals, universities, government, and other research institutions in an educational three day networking opportunity in San Diego, CA, December 4-6, 2012.
Quorum Regulatory Attorney, Mitchell Parrish, JD, CIP, will be co-presenting on “Ethical Issues Involving Third Parties and Secondary Subjects in Research,” Tuesday, December 4, during the Didactic Sessions and Workshops Series A from 10:30am – 11:45am. With several notable faculty involved, curriculum will cover:
- Identification of when pregnant partners, caregivers, and other third parties are research subjects under DHHS and FDA regulations and guidelines
- IRB interpretation of protocol and consent form language considerations that implicate third parties or secondary subjects
- Confidentiality, Health Insurance Portability and Accountability Act (HIPAA), and informed consent considerations for third parties
In the Sails Pavilion exhibit hall, conference attendees are invited to visit with Quorum’s Regulatory Attorneys and Business Development Executives at Booth #25.
Mitchell Parrish, JD, CIP – Quorum Review Regulatory Attorney
Mitchell Parrish joined Quorum Review IRB in January 2010 as an Attorney in Quorum’s Regulatory Department. Prior to Quorum, Mr. Parrish worked as Regulatory Counsel for Western IRB and as a Regulatory Advisor to the National Cancer Institute’s Central IRB.
Mr. Parrish earned his Juris Doctor from the University of Oregon School of Law and is a member of the Washington State Bar, including the Health and Corporate Law sections. Additionally, Mr. Parrish is a member of the American Bar Association and is a Certified Institutional Review Board Professional (CIP).