Book a complimentary review
Start that discussion, and realise the difference!
Contact us and speak to our Clinical & Regulatory Affairs Director at CLIN-r+, Jacqueline van Druten (MICR.CIM.RD) leads a team of consultants and advisors who provide data-driven solutions for medical device regulation.
CLIN-r+ ensures that your business and personal details will be safeguarded and never distributed to third parties.
You should contact us if
- You don’t have the in-house resources or expertise.
- You have deficiency findings.
- You need support transition from MDD to EU MDR.
- You want to work with a consultancy that’s an extension of your business.
Find us
CLIN-r+ Ltd, 1 St.
Katharine’s Way
London E1W 1UN
Innovate and create
impactful, market-leading
devices
Develop successful technologies
for healthcare that payers fund and
regulators approve
Effectively manage
regulatory barriers and outpace
competitors to expand your
market share
