Erwin is regulatory affairs  manager for Peercode’s medical device software. Additional roles are medical device consultant and quality manager. Erwin is part of Peercode’s Regulatory and Quality Team.

Erwin gained international experience with medical device registration projects when working for different large and small pharmaceutical and med tech companies. Erwin has experience as a global project lead for technical documentation and submission strategies and participated in health authority and Notified Bodies consultations and audits. The projects ranged from self-registration Class I products to Class III and drug-device combination products. Erwin is trained on GCP, GMP, Quality and Risk Management (ISO 13485/9001 and 14971) and auditing.

Erwin has also gained wide experience as regulatory and quality consultant. Erwin has presented at conferences, provided training on medical devices regulatory topics, written several white papers and is a member of RAPS. Erwin is medical biologist by training and holds a PhD in Medical Sciences. Erwin is enthusiastic about helping Peercode and its clients to gain regulatory and quality success.

Visit our Peercode Regulatory Consultancy website for more information about our quality-, law- and regulatory-based services in the field of medical devices.