Job title, company, and location:
Managing Director, Peritus Regulatory Consulting Ltd, UK
Biography:
Teresa brings 30 years of medical device and Quality Management Systems experience to her consultancy. She has previously held roles as Head of Approved Body and Quality and Accreditation Director for LNE-GMED UK, a subsidiary of the French Notified Body GMED, setting up an Approved Body. Prior to this position, Teresa worked in the contact lens manufacturing sector and then spent 20 years at BSI in a variety of progressive roles involving auditing, scheme management, certification and latterly operational management. Throughout her career, she has been deeply involved in a number of regulatory challenges such as MDSAP introduction, standards transitions, designation of a new Notified Body, MDR and IVDR implementation, and COVID-19 business continuity planning. Teresa has presented at industry conferences, such as RAPS, with a specialism in Quality Management Systems and development of remote auditing and is currently a member of BSI CH/210/1 Technical Committee responsible for the development of Quality Management Systems in Medical Devices.
Areas of expertise:
Quality Management Systems, ISO 13485, ISO 9001, EU MDR 2017/745, UK MDR 2002 (as amended), MDSAP, ISO/IEC 17021-1 and ISO/IEC 17065
Regulatory jurisdictions covered:
EU, UK, USA, Canada, Australia, Japan, Brazil
Education:
BSc. MSc.
Certifications:
Lead Auditor
Webinars:
https://globalregulatorypress.com/services/medical-device-podcasts/the-ukca-now-next-navigating-ahead/ (October 2025)
Professional/social links:
LinkedIn personal: https://www.linkedin.com/in/teresa~perry/
LinkedIn company: https://www.linkedin.com/company/peritus-regulatory-consulting-ltd/
Website: https://www.peritusregulatory.co.uk/
