Advisory + Staffing Services

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Reliant Life Sciences

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Reliant Life Sciences

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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

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Reliant Life Sciences

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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.

In Vitro Diagnostic Medical Devices Regulation

The EU In Vitro Diagnostic Medical Device Regulation (IVDR) deadline is May 2022, which is fast approaching.

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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

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

The regulation holds several new requirements that must be adhered to:

  • Implementation of a Quality Management System, with a Conformity Assessment
  • New classification system supported by the Conformity Assessment
  • Requirements for CE marking on the device supported by technical documentation
  • Compliance with reporting of clinical investigations and post-market surveillance requirements
  • Appointing an Authorized Representative that is responsible for regulatory compliance

Manufacturers of currently approved in vitro diagnostic medical devices will have a transition time of five years, up to May 26, 2022 to meet the requirements of the IVDR.

Reliant can offer a scalable turn-key solution and services that will enable small and medium-sized medical device companies to comply with the new regulations listed above.