SARWAR Anjum

4 declared company affiliations

Source: EUDAMED

Public regulatory data · synced 2026-09-09

20%

SARWAR Anjum is a Person Responsible for Regulatory Compliance (PRRC) in the medical device industry. Currently affiliated with ANESTHESIA MEDICAL. Explore their full professional profile and affiliations on MD Atlas.

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Company affiliations

PRRC — Person Responsible for Regulatory Compliance
The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.
View in glossary →
Source: EUDAMED · non-removable
PRRC — Person Responsible for Regulatory Compliance
The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.
View in glossary →
1. Appropriate check of the conformity of the aforementioned devices in accordance with the quality management system under which such devices are manufactured and before such device is released 2. Drawing up and keeping up to date of the technical documentation and the EU declaration of conformity of aforementioned devices 3. Fulfillment of the post-market surveillance obligations in accordance with Article 10(10) 4. Fulfillment of reporting obligations referred to in Articles 87 to 91
Source: EUDAMED · non-removable
PRRC — Person Responsible for Regulatory Compliance
The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.
View in glossary →
Check the conformity of devices with quality management system (QMS) procedures before they are released and make sure all technical documentations and Declarations of Conformity are up to date in compliance with MDR 2017/745. Ensure all post-market surveillance and reporting obligations are met.
Source: EUDAMED · non-removable
PRRC — Person Responsible for Regulatory Compliance
The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.
View in glossary →
1. Ensure Actor Registration & SRN Oversight 2. Ensure UDI & Device Registration Compliance 3. Ensure Notified Body & Certificate Data (if applicable) 4. Ensure Vigilance & PMS Data Accuracy 5. Ensure Clinical / Performance Data Consistency 6. Ensure Data Integrity & Compliance Control 7. Ensure Change Management 8. Ensure Coordination with Authorized Representative 9. Ensure Audit & Inspection Readiness
Source: EUDAMED · non-removable

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Company affiliations

PRRC — Person Responsible for Regulatory Compliance
The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.
View in glossary →
Source: EUDAMED · non-removable
PRRC — Person Responsible for Regulatory Compliance
The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.
View in glossary →
1. Appropriate check of the conformity of the aforementioned devices in accordance with the quality management system under which such devices are manufactured and before such device is released 2. Drawing up and keeping up to date of the technical documentation and the EU declaration of conformity of aforementioned devices 3. Fulfillment of the post-market surveillance obligations in accordance with Article 10(10) 4. Fulfillment of reporting obligations referred to in Articles 87 to 91
Source: EUDAMED · non-removable
PRRC — Person Responsible for Regulatory Compliance
The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.
View in glossary →
Check the conformity of devices with quality management system (QMS) procedures before they are released and make sure all technical documentations and Declarations of Conformity are up to date in compliance with MDR 2017/745. Ensure all post-market surveillance and reporting obligations are met.
Source: EUDAMED · non-removable
PRRC — Person Responsible for Regulatory Compliance
The PRRC is the qualified individual a manufacturer or authorised representative must have on hand to ensure ongoing regulatory compliance.
View in glossary →
1. Ensure Actor Registration & SRN Oversight 2. Ensure UDI & Device Registration Compliance 3. Ensure Notified Body & Certificate Data (if applicable) 4. Ensure Vigilance & PMS Data Accuracy 5. Ensure Clinical / Performance Data Consistency 6. Ensure Data Integrity & Compliance Control 7. Ensure Change Management 8. Ensure Coordination with Authorized Representative 9. Ensure Audit & Inspection Readiness
Source: EUDAMED · non-removable

SARWAR Anjum

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