Kelly heads K2 Consulting (www.k2rim.com), a specialty firm focused on Regulatory Affairs, and has over 20 years’ experience in the pharmaceutical industry leading both IT and RIM/Reg Ops organizations in several companies including Wyeth, Pfizer, Shire and Teva. Kelly is actively involved in the EU implementation of IDMP as a member of the SPOR Task Force and its PMS sub-team and is also involved in ISO TC/215. Kelly has been an IRISS member since 2014 and is on the leadership team for the IDMP Topic Group.
Please join me in welcoming Kelly to our team!
Sue Metz
IRISS Forum CEO