Identifying the PRRC for your company is a most important requirement that applies to the European Union and is a core area of responsibility for a person or persons under the Medical device regulation, or In vitro device regulation . The directive to appoint the PRRC also depends on the size of the organization. This is mandatory requirement for any CE Marking under the new EU MDR
The motivation for Identifying the PRRC positions is so that there is a qualified regulatory expert directly responsible for the manufacturing and the market surveillance and reporting systems to ensure the company is meeting the European Union requirements. Companies are not limited to one PRRC and the responsibilities can be allocated to several people, as long as the requirements concerning qualification are met and the distribution of the respective areas of responsibility are documented. If the responsibilities are divided among more than one person, ensure that all responsibilities are covered.

Identifying the PRRC
He should have the right diploma,
He should have 1 year of experience in regulatory affairs or quality management systems on medical devices.
For Identifying the PRRC what Diploma is required?
There is no fix choice but it should be a diploma in:

Law
Medicine
Pharmacy
Engineering
Another Scientific Discipline
Identifying the PRRC Responsibilities
The PRRC has at least 5 responsibilities clearly outline in Article 15.

Checking the conformity of medical devices in accordance with the quality management system (QMS) before the medical device is released;
Drawing up the technical documentation and keeping it up to date; 
Making sure the post-market surveillance obligations are in compliance with EU regulations Article 10(9); 
Fulfilling the reporting obligations referred to in reporting of serious incidents and field safety corrective actions (Article 82) and implementing acts (Article 86)
Ensuring the statement that investigational devices (Section 4.1 of Annex XIV) meet the GSPRs is signed. 
Read More - Identifying the PRRC
Read More Article -
1. Orthopedic Implants Manufacturing
2. disposable syringe manufacturers
3. Dental Implants Manufacturing
4.Blood Collection Tubes Manufacturing

Contact details –
Phone no - 9325283428
Mail - [email protected]

If You Want Medical Devices Services Consultation For Following.

1. Medical Device Manufacturing
2. CDSCO Registration
3. FDA 510 k clearance
4. Continuous Improvement Program
5. Design Control Requirements
6. QMS Certification Services
7. Manufacturing Plant Layout Design
8. Primary Packaging Consultant
9. Manufacturing Site Conceptualization
10. Combination Product
11. Medical Device Design And Development
12. Clean Room Design Consultant
13. ISO 13485 Certification
14. ISO 15378 certification
15. Medical Device Process Validation
16. 21 cfr part 820
17. 21 cfr part 210 and 211
18. DMF submission
19. CAPA Management
10. TURNKEY PROJECT CONSULTANT