Meet...

Theresa Jeary

Presenter

Theresa Jeary holds a Master’s Degree in Pharmaceutical Science and is eligible to be a Pharmaceutical Qualified Person. Theresa has over 25 years’ experience working in both the Pharmaceutical and Medical Device industries and has worked in a variety of roles across the full development cycle from product concept and early stage development, process transfer, validation and regulatory departments, and has been involved in the development of many commercially available medicinal and medical device products.

She has over 10 years Notified Body experience working at BSi as a technical expert and until January held the position of Head of Notified Body at LRQA. Her area of technical expertise is in device-drug combinations and borderline classifications, and she has completed many successful consultations in this area with many European Competent Authorities and EMA.

Theresa now works as a consultant to the Pharmaceutical and Medical device sectors and is a frequently invited speaker on medical device legislation and combination products.

Theresa Jeary’s courses

Reviews for Theresa’s courses

Was very useful. I feel I accomplished further knowledge about the implementation of MDR and IVDR and also what is on the horizon in terms of the UK regulations from the course. The content of update on IVDR was great as it was directly related to my work. I also enjoyed learning more about the history of the regulations/legislative process and gained some useful background knowledge on combination products.

30 Apr 2025

A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK

Management Forum have become my go-to provider of life science training. They always find excellent speakers who present their subject matter in a very knowledgeable, complete and thoroughly enjoyable way. I have always found Management Forum courses to be excellent value for money and the New Medical Device Regulation course was no exception.

24 Sep 2019

A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK

A relaxed, open forum where you felt comfortable to ask any questions you needed through the presentations and the day. The speakers were all very clear, concise, factual and interactive.

24 Sep 2019

A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK

Very well run, met my objectives, and speakers were interesting, approachable and very knowledgeable.

24 Sep 2019

A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK

The speakers were very professional and knowledgeable. They delivered the content in an easy format and allowed plenty of time for questions and interaction from the attendees.
I particularly liked the section regarding the context of the regulation and background to its development which will help me when explaining this to my clients.

24 Sep 2019

A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK

Excellent training performed by very knowledgeable speakers.

6 Mar 2019

A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK

Good, complete coverage of the new regulations. Good anticipating on discussed items.

25 Sep 2018

A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK

[The speakers were] all very knowledgeable. The whole course was very reassuring with the 'big monster' of the MDR being broken down so that it appears manageable and less scary. It was full of helpful advice both general and specific to my products.

25 Sep 2018

A Regulatory Update on the Medical Device and In-Vitro Diagnostic Regulations in the EU and UK