GCP, GMP, GxP Medical Device Auditors

+91 98100 68241

bd@Crqa.in

YOUR TRUSTED PARTNERS FOR QUALITY ASSURANCE AND REGULATORY SERVICES

EXCELLENCE IN AUDITING, REGULATORY CONSULTING, AND GLOBAL COMPLIANCE SOLUTIONS

YOUR TRUSTED PARTNERS FOR GXP AUDITING SERVICES

YOUR TRUSTED PARTNERS FOR QUALITY ASSURANCE AND REGULATORY SERVICES

Webinar and Training
EXCELLENCE IN AUDITING, REGULATORY CONSULTING, AND GLOBAL COMPLIANCE SOLUTIONS

Webinar and Training
YOUR TRUSTED PARTNERS FOR GXP AUDITING SERVICES

Webinar and Training

Pharmaceutical Quality Management Services

PQMS offers following services which are designed based on Client- specific needs to achieve Total Quality Compliance (TQC) :

Site Quality Audit Services - This service will include Pre , Post or Regular Quality system audit of a site for the suitability of manufacturing & Testing/Release of the product at this site. This will generate a comprehensive report of the Audit covering the different critical functions performed at the site like, Stores (RM/PM/Quarantine), Quality control ( Test methods and specifications used to test the manufactured batch, instrument calibration status), Production ( manufacturing process used, validation status of the process used, etc.) Stability Protocol/ Facility, Personnel Training, Equipment Maintenance, etc. functions to ensure the Quality Compliance of site towards manufacture & Testing / Release of the product from the site for sales.
This Quality Audit of the Site will ensure compliance of each of the manufactured batch at the site and hence will save cost of recall & destruction of a non-compliant/ failed batch of product, cost of investigation and trouble shooting of the complaints, cost of losing image of the brand/Company.
Product Registration Dossier Management - PQMS will take up complete responsibility of Registration Dossier preparation, submission and query handling as per the Client needs and Formats. This will include CTD, Non-CTD, ACTD, any other format.
Independent Quality Audits (IQA) – PQMS will carry out in-depth audit of the Quality control Laboratory function to help you receive various regulatory authorities Compliance
Quality Document Management (QDM) – PQMS can on-line Prepare & Review all Quality Documents like Batch Manufacturing & Packing records, Validation Protocols/ Reports, Stability Studies Report/Data compilation, any other Summary/ Report preparation as per your needs to significantly reduce your cost & time towards these mandatory regulatory tasks.
Training – Training to your people on any Quality topic as per your Training Calendar and Training Matter. This service will save your valuable Resources/Time towards Regulatory Compliance towards the Employee Training requirements. PQMS can take up Annual / Long-Term Contract for this Service.

For more information on our services, please contact us +91 98100 68241 or mail @ bd@crqa.in

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