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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

Pharmacovigilance

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Monitoring Adverse Drug Reaction

Adverse drug reactions are closely monitored by Health Canada

Post-market monitoring of drugs (pharmacovigilance) is audited separately by Health Canada. This process encompasses not only quality team, but also sales, marketing and customer service teams: Any person that is in contact with a complaint relating to an adverse drug reaction has a part in in the process.

Atinza will ensure that client’s reports are prepared and submitted within the required timeframes and meet all Health Canada’s requirements.

Drug Recall

A drug recall typically involves removal of the product from the market and its destruction.

During a recall, Health Canada works closely with the recalling firm (which can be a manufacturer, importer, brand owner, or distributor) to ensure that the recall strategy and communication meet the minimum standards of communication.

Atinza will support clients to ensure that all affected customers are identified and notified promptly, and appropriate documentation is submitted to Health Canada on time to reduce clients’ losses and minimal disruption to client’s business.

Post marketing support

Atinza provide complete post marketing support that is customized according to client's requirements:
  • In the case of recall or complain, Atinza can communicate with Health Canada on behalf of the clients and monitoring deadlines for the clients
  • In the case of an out-of-specification result, complaint, or recall, Atinza will assess the risk and provide customized guidance to the clients, ensuring that the issue is handled efficiently and correctly.
  • Communicate with Health Canada on behalf of clients.
  • Guidance services
  • Timely response to inquiries of Health Canada on behalf of the clients
  • Communicate with suppliers and customers of clients to coordinate all correspondence and fulfill tractability requirements.

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Please let us know if you have any inquiries.

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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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