Frits Stulp is the managing director of Iperion Life Sciences Consultancy. With over 20 years of experience in the life sciences industry, he has worked on multiple regulatory compliance projects, becoming an IDMP SME program manager and adviser to several high-profile pharmaceutical companies, regulatory authorities and software suppliers. He is currently the project manager for the EU Substance Registration System (MEB/EMA); is an active member of the EMA ISO IDMP Task Force for Substances and Products; and is the IRISS Forum IDMP topic lead. He holds an MSc in pharmacochemistry from the Free University of Amsterdam. 

Frits Stulp

Articles

2019 saw progress towards ISO Identification of Medicinal Products data standards implementation, but making patients front and central to project focus must remain a priority, says Frits Stulp.


IDMP: Making Patients the Priority in 2020

It is worth keeping patients, clinicians, pharmacists and the wider public front of mind when evaluating priorities and best next steps towards Identification of Medicinal Products(IMDP) and other emerging standards, writes Frits Stulp.

Author | Frits Stulp