Our commitment to continuous learning in the area of: Medical Device Lifecycle and Regulation
One of our company values is professionalism, and we pride ourselves on continuing to develop
our skills and knowledge so we can provide a world class, professional service to our clients.
Our team is encouraged to dedicate time to learning each week to improve their individual areas
of expertise, and this goes for our leadership team, too.
Last week, our CEO David Lawson attended Regulatory & Related Activities Through the
Device Lifecycle, a course facilitated by The Organisation for Professionals in Regulatory Affairs
Given David’s extensive experience in regulatory affairs and compliance testing, this course
was useful in further expanding our team’s existing knowledge in the following areas:
- Applying critical analysis to the legal and regulatory requirements applying to medical devices
- Dealing with complex issues, make sound judgments in the absence of complete data, and communicate conclusions clearly to specialist and non- specialist audiences
- Demonstrating a critical understanding of the factors required to maximise the success of a medical device, health technology assessment and reimbursement
This supports the work that we already perform for our clients in regulatory engagement,
consultancy and compliance testing for medical devices while also allowing us to continue
expanding the services we are able to provide to our clients.
For further information on the regulations and compliance testing work that we do in
pharmaceutical medical devices, with next generation nicotine products and CBD products,
contact firstname.lastname@example.org or click here to learn more about the services we offer.