Verify UKRP Status - NOVAREG (UK)

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NOVAREG (UK)

Medical Device Consultants in UK

+44 75 8147 1399
enquiry@novareg.co.uk

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UKCA MARK
- UK RESPONSIBLE PERSON (UKRP)
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  - STERILIZATION PROCESS
  - SOFTWARE DEVICE 510K PROCESS
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CONTACT US

HOME
ABOUT US
UKCA MARK
- UK RESPONSIBLE PERSON (UKRP)
- UKCA MARKING
EU CE MARK
US FDA
- FDA 510(k)
  - STERILIZATION PROCESS
  - SOFTWARE DEVICE 510K PROCESS
- FDA REGISTRATION
BLOG
CONTACT US

VERIFY UKRP AGREEMENT STATUS

Organisation First Name:

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Our Company

We help organizations to overcome regulatory hurdles by sharing, guiding, training and developing documents that of high quality, economically viable and assurance of clearance.

As knowledge driven team in UK, we aim to be strategic outsourced partners to customers, we strive to build an good long lasting tie up with every customers who provide business to us. Continue to be curious and constantly educate our self in new ways of solving new regulatory requirements .

One step ahead. All the time.

Recent Post

Demonstration of Equivalence Clinical Aspects
January 21, 2025
Successful Clinical Evaluation Report under MDR 2017/745
January 21, 2025
Clinical Evaluation Of Reusable, Measuring and Sterile Class I Medical Devices
January 11, 2025
Do Toys Need a CE Mark? Detailed Overview
January 8, 2025

Corporate Office

Office 54, No:58, Peregrine Road, Hainault,
Ilford, Essex, England. IG6 3SZ. United Kingdom
Landline No: + 44 13 2241 3787
Mobile No: + 44 75 8147 1399
Email : ukrp@novareg.co.uk

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