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WELCOME TO Quality Medical Regulations Services (QMRS) | ||||||
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QMRS prepares, compile, and submit product registration packages (Generic drugs, Cosmetic, NHPs, Novel food etc.) as per Health Canada Requirements. Please CLICK HERE to continue. |
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QMRS conducts “Third Party Audit” to assess the degree to which the facility is fulfilling the applicable GMPs requirements.We provide a "Certificate of GMP Compliance”, if the facility found to be fulfilling the GMP requirements. Please CLICK HERE to continue. |
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GOOD DOCUMENTATION PRACTICES (GDPs) QMRS provides assistance to establish the needed SOPs and all other documentation requirements pertaining to GMPs and Good Clinical Practices. Our documents are written according to the FDA, Health Canada, ICH, and WHO Guidelines. Please CLICK HERE to continue. |
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HAZARD ANALYSIS
CRITICAL CONTROL POINT (HACCP) QMRS assess the adequacy of the facility prerequisite programs and design & develop the format of successful HACCP plans. QMRS issue a “Certificate of HACCP Compliance”, if the facility found to be fulfilling the HACCP system requirements. Please click HACCP to continue. |
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QMRS provides GMP training on drug, dietary supplements and
NHPs regulations. Also, on Good Documentation Practices, and HACCP. |
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QMRS On-Line documents, (SOPs and policies) are on Drug GMPs and Good Clinical Practices (GCPs) These documents cover almost all manufacturing processes and clinical trials activities as required by regulatory authorities and the ICH. To order any of these documents, please CLICK HERE. |
Quality Medical Regulations Services
196 Annapolis Circle, Ottawa; Ontario K1V 1Z1 CANADA
email: info@qmrs.com, Telephone: 613-526 0471, Fax: 613-526 0558