Susan Metz

Susan Metz

Susan Metz

Principal Consultant, IDMP

Sue is a subject matter expert in xEVMPD, IDMP and regulatory information management with Parexel. Most recently, Sue has been responsible for developing and delivering gap assessment strategies and driving the planning, development, and implementation strategy for IDMP clients. She is a standing member of the EU ISO IDMP Task Force, the US TAG ISO/TC 215/WG6 and is on the IRISS IDMP Leadership Team.

Work Experience

Sue has over 30 years of experience defining and designing life sciences software and services, for regulatory affairs, regulatory operations, sales and marketing in pharmaceutical, biologics, veterinary, consumer and medical device organizations.

She has been responsible for translating global regulatory requirements into process and software requirements and designs for Parexel’s InSight Regulatory Information Management system along with high level strategy and design for the upcoming InSight for IDMP module and designing data assessment strategies for IDMP initiatives.

We are always available for a conversation.