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Compliance & audits

Quality Management Services (QMS) implementation is required by each and every firm whether it is medical device industry, pharmaceutical, food etc. Implementation of QMS is necessary as these are being followed and had been made mandatory by European countries, US. Implementing the QMS not only implements the processes in your organization but also boost up each and every are of your facility. It is also a quality standard and is mandatory if you’re thinking of putting your products for commercial distribution in international market.

Med devices have been accredited by for its services quality management services. We have our own quality auditors that help you in QMS implementations by on site Audits. We offer our services for:

  • ISO 9001:2008,
  • ISO 13485:2012,
  • GMP, GLP, WHO GMP,GCP
  • FDA compliance inspection (21 CFR 820, 21 CFR 807)

After the successful audit, certificate will be issued to your Organization for the audit compliance.

Testimonials

  • I would like to thank entire team of Meddevices for your assistance and guidance in obtaining ISO & CE certification. Your help will be instrumental in our continued growth & success.

    Arul Pragyasam
  • Thank you Meddevices! They have tackled all aspects of my CE case in a very short period of time. They are by far the best team I have worked with..

    Karen Roberston
  • I wouldn’t think of facing an FDA audit without Meddevices’s Assistance..

    Gerhard frick
  • I deeply appreciate the outstanding service that Meddevices have provided us over the last ten years..

    Gregony Denton

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Company Info

MED DEVICES LIFESCIENCES LIMITED was formed to provide medical device manufacturers world-wide with flexible and well adjusted service packages to assist its clients to comply with EU & US legislation .

Med Devices 123 fifth Avenue
New York, NY 10160
Ph: +19142942185
Email: info@meddevices.com
                        

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