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HM-DIN – Homeopathic medicines are licensed as DIN-HM in Canada. DIN (Drug Identification Number) is a number issued by Health Canada to a drug product to be sold in Canada. The number identifies all drug products sold in dosage and is located on the label of prescription drug products that have been evaluated and authorized for sale in Canada. Having this number is mandatory to sell your homeopathic medicines.
NDC – NDC (National Drug Code) is a unique three-segment number assigned by FDA. It serves as a universal product identifier for drugs and helps consumers and compliance/enforcement professionals to identify product medicine. The number also identifies the pharmaceutical firm/repackager, or distributor/, the Drug – Sunscreen with the active ingredient and the package type and size.
Proven Expertise. Companies who have Trusted Us to Become Regulatory Compliant with Health Canada
I have been working with Andrew and his team at QSS for a couple of years now. I have clients from many different parts of the world and each situation requires expertise and focus, which I’m getting from QSS. I highly recommend Andrew and QSS to any perspective client who wants to “get it right” regarding Canadian and cross border compliance.
No drug products in Canada or USA are permitted to be sold without meeting Homeopathic Compliance Solutions. In case, a product that is classified as a drug under the Food and Drugs Act and is marketed without a DIN does not comply with the Health Canada regulations. Similarly, in USA, drugs without NDC are thought to have significant risks to patients, because they have not been reviewed by the FDA for effectiveness, safety and quality. Having HM-DIN in Canada and NDC in USA let patients know that the drugs have been manufactured in a way that guarantees the quality of the product or whether their label is complete and accurate.
This Act requires registered drug establishments to provide FDA with a current list of all drugs manufactured, propagated, prepared, compounded, or processed by it for commercial sale or distribution.
Drug products in USA are identified and reported using the National Drug Code.
In Canada, the Medicinal ingredient must be found in the homeopathic monograph and one of the homeopathic pharmacopeia such as the Homeopathic Pharmacopeia of HPUS, European Pharmacopeia (Ph. Eur) among others.
Homeopathic medicine labels must be bilingual i.e. both in English and in French because these languages are considered official in Canada.
Our Canadian homeopathic compliance experts provide turnkey solutions to meet regulatory compliance.
HM-DIN Registration
We'll help you in licensing for non-specific health claim based HM-DINs class 1 NHP process and licensing for specific health claims class 3 NHP licensing process and documentation for submission.
HM-DIN Package Compliance and French Translation
Worried about HM-DIN Package Compliance and French Translation? Our experts will help you meet packaging compliance by making homeopathic medicine labels bilingual (English and French) and meeting Canadian labelling laws.
Quick assistance at the right time to meet homeopathic drug regulations in USA. Our range of homeopathic drugs resolutions in USA include:
Get full-services to register NDC Labeler Code. Our experts will help you prepare and submit a request in SPL (Structured Product Labeling) for NDC registration.
We’ll help you in US Drug Listing and registering your drugs and submitting required listing information for all homeopathic medicines.
Leverage our expertise to meet US Drug Label Compliance for homeopathic medicines and be aware of changes to labelling compliance.
We will help you in the application process for establishment registration SPL and submitting to the FDA through ESG gateway.
Get in touch with us as we will work as your US Agent and respond to FDA questions. We will also help you during meetings with FDA officials.
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Quality Smart Solutions is a global consulting firm, engaged in providing strategic support for products including NHPs, pharmaceuticals, and medical devices, in areas such as Regulatory Support, Site Licensing, Clinical Development and more.