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Technovigilance is in charge of monitoring the safety of Medical Devices and this, in turn, is a set of activities where all

At the end of last January 2023, Cofepris published on its website and on social networks its Regulatory Certainty Strategy for the

Cfepris

ICH is the International Council of Harmonization of Technical Requirements for Pharmaceuticals for Human Use (Consejo Internacional de Armonización de Requisitos Técnicos

WHODrug

WHODrug is a drug product dictionary, used to identify drug product’s names and review drug product’s information, including drug substances (active ingredients),

The commercialization of products classified as food supplements is very common in Mexico. But what kind of products are classified as food

General Health Law (Ley General de Salud -LGS), provides the general frame of regulation and describes all that is considered a medical

Experts in consulting and regulatory and pharmacovigilance intelligence in Mexico. Specialists in approvals for drugs, medical devices and other products and services within Cofepris.

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