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      • NHP Documentation Review
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      • Natural Health Product Site Licence
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Atinza Canada Inc.Atinza Canada Inc.
  • Home
  • Global Regulatory Affairs Services
    • Introduction
    • Pharmaceutical
      • Requirements of Health Authorities
      • Drug Application Process
      • Meeting with Health Authorities
      • Electronic Common Technical Document (eCTD)
      • Register of Innovative Drugs
      • Submissions Comparing to Innovative Drugs
      • Product Monograph
      • Drug Label Compliance
      • Filing of Information and Material to Health Authorities
      • Evaluation of Submissions
      • Pharmacovigilance
    • Natural Health Products
      • NHP Documentation Review
      • NHP Product Registration Submissions
      • Natural Health Product Site Licence
    • Medical Device
      • Medical Devices Services
      • Medical Device Application Process
      • Medical Device class II, III and IV
  • Market Expansion Services
  • Contact Us

Natural Health Product Site Licence

Home PharmaceuticalNatural Health Product Site Licence

Natural Health Product (NHP) Site Licence Inspection

Adverse drug reactions are closely monitored by Health Canada

In order to obtain and maintain a Natural Health Product site license for manufacturing, packaging, labeling, or importing natural health products (NHPs), applicants must attest to and provide proof of compliance with Good Manufacturing Practices (GMPs). Distributors and foreign manufacturers of NHPs are also expected to follow GMPs. Atinza can audit client’s/client’s foreign suppliers’ existing facilities, procedures and records, or support clients to design and implement GMP-compliant procedures prior to applying for NHP Site license.

Good Manufacturing Practice for NHP

Good Manufacturing Practices (GMPs) must be employed to ensure NHP's safety and quality.

Appropriate standards and practices are administered regarding NHP’s manufacture, storage, handling and distribution, including, but not limited, to: specifications (of NHP), premises, equipment, personnel, sanitation program, operations, quality assurance, stability, records, sterile products, lot or batch samples, and recall reporting.

 

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Global Expertise in Regulatory Affairs Experienced & Results-Oriented

Atinza provides timely but yet effective regulatory affairs services for all stages of your products’ development and lifecycle management.



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