Advisory + Staffing Services

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Reliant Life Sciences

Schedule a Consultation

Schedule a few minutes to connect with an expert regarding your project’s advisory and/or staffing needs. Don’t worry, we’ll never spam you.

Send a Message
Reliant Life Sciences

Send a Message

Send us a message to connect with an expert regarding our advisory and staffing capabilities. Don’t worry, we’ll never spam you.

Consultant Opportunities

Connect with a Recruiter
Reliant Life Sciences

Connect with a Recruiter

Complete the following form to connect with a Reliant Life Sciences recruiter regarding opportunities that match your skills and interests. Don’t worry, we’ll never spam you.

Sign-up for Job Alerts
Reliant Life Sciences

Sign-up for Job Alerts

Complete the following form and our team will email you opportunities that match your skills and interests. Don’t worry, we’ll never spam you.

Advisory + Staffing Services

Schedule a Consultation
Reliant Life Sciences

Schedule a Consultation

Schedule a few minutes to connect with an expert regarding your project’s advisory and/or staffing needs. Don’t worry, we’ll never spam you.

Send a Message
Reliant Life Sciences

Send a Message

Send us a message to connect with an expert regarding our advisory and staffing capabilities. Don’t worry, we’ll never spam you.

Consultant Opportunities

Connect with a Recruiter
Reliant Life Sciences

Connect with a Recruiter

Complete the following form to connect with a Reliant Life Sciences recruiter regarding opportunities that match your skills and interests. Don’t worry, we’ll never spam you.

Sign-up for Job Alerts
Reliant Life Sciences

Sign-up for Job Alerts

Complete the following form and our team will email you opportunities that match your skills and interests. Don’t worry, we’ll never spam you.

Determining if a Standard has been Harmonized under the scope of EU MDR

Are you trying to determine if one of the standards under your quality management system is recognized under the European Medical Device Regulation or EU MDR (2017/745)? Don’t worry, we got the answers right here! In partnership with MDR Consultants, here are a few pointers on how to find and verify your standards.

The Basics

According to Section 1. Article 8. of the EU MDR Regulation 2017/745, any standard must be published in the C-series of the Official Journal of the European Union before it can be used as a method, basis, or means of conformity to regulation.

Before a medical device company can use a standard in any process or product under the organization’s quality management system to show conformity to regulation, the organization must confirm the standard has been harmonized under the EU MDR scope.

Has Your Standard Been Harmonized?

So how do you find out if your standard has been harmonized?

There are a few different ways to search the records of the Official Journal of the European Union for this information:

Additionally, the European Commission has created a page on its website that provides a consolidated list of the progress of harmonization of medical device-related standards. You can find this webpage here or by accessing the summary document directly.

If you did not find your standard in any of these sections, your standard is not harmonized under the EU MDR, and you must either select a new standard, find another method as a basis to conformity, or develop and document a rationale on why the use of the standard represents state of the art. 

MDR Training Programs

The deadline to transition to the EU MDR is May 26, 2024. Are you looking for information on how to start the transition or how to best structure your organization?

Reliant Life Sciences has partnered with MDR Consultants and Isabel Osario to offer hands-on training. To learn more and to sign up, please visit their website