2020-08-04T17:13:23+00:00December 23rd, 2018|
  • Application: The applicant must complete a permit application form for marking food products with the appropriate GMP conditions symbol, provide the required documents and submit them to the unit for adequate production conditions in the National Food Service.
  • Examination of the application: Upon receipt of the application, and assuming that the documents are valid, the application will be referred for the Health Bureau’s opinion. The decision to audit or inspect the factory is at the discretion of the district engineer.
  • Document completion: If, after reviewing the documents, there are any missing documents, a document completion request will be sent to the factory. Once the documents have been submitted completed, the process will continue.
  • Issue permit: For food establishments and nutritional supplements that meet the requirements, a permit will be issued to mark the food products with the GMP symbol.

Product Development, Delivery System & Clinical Trials

Novel cannabis products and delivery system for improved bio-availability, accuracy, consistency and efficacy that can be proven and backed up with a strong IP and clinical trials

Growing, Manufacturing & Lab Facilities Design

Conceptual & detailed design including personnel/material flow diagram, pressure cascade, cleanness level, utilities and technology based on current GxP standards and common practices

Quality Assurance & Good Practices (GxP)

An effective quality management system establishment, policies and SOPs writing, cultivation and manufacturing procedures, protocols and employees training

Cultivation & Product Manufacturing Technology

Utilities, systems, machinery and controls required for cultivation, development and manufacturing processes that will enable high quality, control and cost-effectiveness.

New Product Regulations & Submissions

Cannabis products specifications and regulatory requirements completion including all relevant documentation and data in order to be submitted and sold in regulatory markets

Qualification &Validation

New facility, infrastructure, utilities, system, machinery, software, control system, manufacturing/cleaning processes qualification and validation protocols, execution and reports

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