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WELCOME TO Quality Medical Regulations Services (QMRS) | ||||||
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QMRS prepare, compile, and submit product registration packages as per Health Canada requirements.
We could be your regulatory representative in Canada in order to
obtain the market authorization (licensing) for prescribed and non
prescribed products
(Generic drugs, Cosmetic, NHPs,
Novel food etc.) Please CLICK HERE TO CONTINUE |
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SITE (ESTABLISHMENT) LICENSING
We (QMRS) conduct “Third Party Audit” to assess the degree
to which your facility is fulfilling the QMRS will award you a “Certificate of Good Manufacturing Practices Compliance”, if the facility found to be fulfilling the current GMPs requirements. We prepare (complete) the Site License Application Form and the “Quality Assurance Report” that needed by Health Canada to receive the site license.
Please CLICK HERE TO CONTINUE |
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GOOD DOCUMENTATION PRACTICES (GDPs)
QMRS can assist you to establish the needed SOPs and all other documentation requirements pertaining to Good Manufacturing Practices and Good Clinical Practices. Please CLICK HERE TO CONTINUE |
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QMRS can issue a “Certificate of HACCP Compliance”, if the facility found to be fulfilling the HACCP system requirements. |
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QMRS provides professional GMPs training (for Drug, Dietary Supplements and Natural Health Products facilities). Also, we provide training on Good Documentation Practices, and HACCPWe issue many types of certificates that needed by regulatory authorities. QMRS HACCP Training Courses are accredited by the “International HACCP Alliance”.
Please CLICK HERE TO CONTINUE |
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QMRS On-Line documents, (SOPs and policies) are on:
These documents cover almost all manufacturing
processes and clinical trials activities as required by regulatory
authorities and the International Conference on Harmonization (ICH). To order any of these documents, please CLICK HERE
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Quality Medical Regulations Services
196 Annapolis Circle, Ottawa; Ontario K1V 1Z1 CANADA
email: info@qmrs.com, Telephone: 613-526 0471, Fax: 613-526 0558