COFEPRIS or the Federal Committee for Protection from Sanitary Risks (Comisión Federal para la Protección contra Riesgos Sanitarios) is the department within the agency that deals with the importation of medical devices and issues advertising permits for these products.

The Therapeutic Goods Administration (TGA) is Australia's regulatory authority for therapeutic goods such as medicines, medical devices, and diagnostic tests.

Medicines and Healthcare products Regulatory Agency (MHRA) of Department of Health of UK Government, ICP has been formally approved by UK MHRA for consistantly maintaining the quality, efficacy and safety of its products.

• La Dirección General de Medicamentos Insumos y Drogas (DIGEMID) es un órgano de línea del Ministerio de Salud, creado con el Decreto Legislativo Nº 584 del 18 de Abril del año 1990.

• La DIGEMID es una institución técnico normativa que tiene como objetivo fundamental, lograr que la población tenga acceso a medicamentos seguros, eficaces y de calidad y que estos sean usados racionalmente, por lo cual ha establecido como política:

• Accreditation: 2021

• The GMP Certificate in Dubai is proof of compliance with the Good Manufacturing Practice Standards followed by the Pharmaceutical Manufacturer.

• Organizations in the field of pharmaceuticals, healthcare sectors, including their buildings, environment, methods of documentation, work procedures, after-sale services, etc. is assessed to ensure quality control and adherence to safety regulations through this certification.

• The Brazilian Health Regulatory Agency (Anvisa) is an organization linked to the Ministry of Health, part of the Brazilian National Health System (SUS) as the coordinator of the Brazilian Health Regulatory System (SNVS).

• Anvisa’s role is to promote the protection of the population’s health by executing sanitary control of the production, marketing and use of products and services subject to health regulation, including related environments, processes, ingredients and technologies.

• Accreditation: 2021

Good Manufacturing Practice (GMP) should be utilised is if the product has an “active ingredient” to ensure that mistakes do not occur. An active ingredient is a substance that causes a physiological response in the body – and since CBD and medicinal cannabis claim to / or are proven to have this effect they are to be considered one (i.e. a medicine).