Site Registration

Activities related to manufacturing, packaging, labelling and importing for most product categories e.g. Natural Health Products, Drugs, Medical Devices etc. require compliance oversight and registration. We assist in bringing your site up to compliance, advise you on regulations and how to optimize operations. We can review and assist in amending existing Standard Operating Procedures or write your processes and control documents in an appropriate format.

We assist in bringing your site up to compliance, advise you on regulations and how to optimize operations. We can review and assist in amending existing Standard Operating Procedures or write your processes and control documents in an appropriate format.

Innovate Phytoceuticals can assist you with the following:

  • NNHPD site licensing for manufacturers, packagers, labelers and importers.
  • Drug establishment licensing for manufacturers, packagers, labelers and importers.
  • Medical device establishment licensing for manufacturers, packagers, labelers and importers.
  • CFIA establishment licensing/registration for importers and interprovincial trade.
  • Cannabis licensing for retail, cultivation, processing and distribution.

Good Manufacturing Practices

All sites are expected to be following Good Manufacturing Practices to ensure the quality of the product they are responsible for. Innovate Phytoceuticals can identify GMP deficiencies and assist you in bringing your site in line with GMP. Innovate Phytoceuticals can also provide training for your site and assist you in documenting ongoing GMP training.

Standard Operating Procedures

Depending on your specific needs Innovate Phytoceuticals can assist you with your Standard Operating Procedures. Some sites may require all SOPs to be written, other require minimal input and just need help with format and requirements. We can tailor our services to meet your requirements.

Quality

There is ongoing scrutiny of raw material quality and adulteration issues. Innovate Phytoceuticals can help you understand what you should be looking for in a raw material supplier and evidence of “good practice” from these suppliers. We can assist you in reviewing specifications, understanding the Certificate of Analysis, create Quality Technical Agreements with your vendors and suppliers and create vendor qualification programs if necessary.

Foreign Site Registration

Are you using a foreign site for the manufacturing of your product or are you a foreign site that needs to be registered in Canada? Either way we can help you through the process of getting the required registration for your activities.

  • FDA site registration
  • Finished product specifications, certificate of analysis and finished product testing