Product Registration

ICCI - International Cannabis and Cannabinoids Institute’s product registration services can facilitate your cannabis product’s entry into a new market. Our experts will guide you through the entire registration process, ensuring compliance with national and international product registration requirements. ICCI’s expertise will not only guide you on how to comply with all applicable laws and norms, but will also save you money, time and stress at every step of the registration process.

In order for a product to be registered, the first step is to ensure national and/or international compliance, depending on government requirements. ICCI provides a full range of product registration services to meet your needs:

Clinical consulting

ICCI consults on and conducts pre-clinical research and clinical trials for cannabis and hemp  products investigating safety and efficacy. Our pre-clinic and clinical research facilities and protocols meet the stringent U.S. FDA and E.U. EMA research standards for pharmaceuticals, nutraceuticals and over-the-counter products. 

Product sampling

ICCI will analyse product samples from different batches to test for lot-to-lot consistency, safety and compliance. When all sample analyses are finalized, the registration process can start. 

International product certification with ICCI’s Patient Focused Certification (PFC) program

Designed to ensure safety, quality and consistency of cannabis and hemp products, PFC is a third-party certification service that ensures  product cultivation, manufacturing, distribution and/or laboratory analysis processes comply with specific national and international standards [e.g. American Herbal Pharmacopoeia (AHP), Americal Herbal Products Association (AHPA), American Chemical Society (ACS), Small Chemical Business (SCHB), Agriculture and Food (AGFD), and Chemical Health & Safety(CH&S), World Health Organization (WHO), European Medicines Agency (EMA), European Herb Growers Association (EUROPAM), and Pharmaceutical Inspection Co-operation Scheme (PIC/S)].  The certification process includes the evaluation of standard operating procedures (SOPs) and the use of generally accepted agricultural, manufacturing and laboratory (GMP) practices. Certification is earned when the company has met all the standards of certification.

Required documentation

ICCI will collect and organize all required content and documentation (e.g. administrative documents, compliance certificates, fees, sample results, mandatory declarations etc.) in preparation for creating your product application dossier. 

Application dossier

Once all the necessary documents are obtained, ICCI will create an application dossier for your product registration. The application dossier includes a detailed product profile, and all required administrative information. 

Product packaging

ICCI will guide you on labelling text for your product to ensure the wording and content is compliant with national and international laws. 

Process monitoring 

ICCI will manage and follow-up on each step of the registration process guiding the company to a successful outcome. 

Marketing plan 

ICCI can create a tailored marketing plan for the distribution, sale and promotion of your product. We will conduct thorough market research and data analysis to develop effective marketing and promotion strategies for your product.


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ICCI Webinar "Introduction to Clinical Trials" with Dr. Martin Votava 27. 11. 2019

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