IPSNEWS
Dietary Supplements: Regulatory Framework in Mexico
Mexico's dietary supplement market is growing rapidly, offering opportunities but also intense competition. Understanding and complying with COFEPRIS regulations is crucial to avoid legal issues. This document outlines these requirements for manufacturers and marketers.
Regulatory Update Lists of additives and adjuvants permitted by COFEPRIS
One of the consultation documents for dietary supplements is the list of additives and adjuvants published by COFEPRIS. These lists have been updated.
Cosmetics: Know the regulation in Mexico
The cosmetics industry in Mexico is subject to a robust regulatory framework enforced by the Federal Commission for Protection against Health Risks (COFEPRIS). This oversight aims to safeguard consumer health and ensure product safety and quality. Given the growing popularity of cosmetics, understanding these regulations is crucial for businesses operating within this sector.
Regulatory Update COFEPRIS Resolves Transfer of Rights within 24 hours
At COFEPRIS's priority lane (VRI) , the transfer of rights for medical devices, pharmaceuticals, pesticides, and plant nutrients will be resolved within 24 business hours, streamlining the process for those involved.
Regulatory Update Proposal to modify the Official Mexican Standard (NOM-137) for medical device labeling (Updated)
The Ministry of Health, through COFEPRIS, released a proposal on March 3rd that aims to modify the Official Mexican Standard NOM-137-SSA1-2008 for medical device labeling.
NAVIGATE THE ADVERTISING LANDSCAPE IN MEXICO WITH CONFIDENCE
COFEPRIS develops and enforces advertising guidelines that ensure product claims are accurate, truthful, and not misleading. This helps to protect consumers from false or exaggerated claims that could influence their purchasing decisions.
IPS launches IPSocial Cause Program
We are thrilled to launch our IPSocial Cause program, an initiative designed to transform the company into a socially responsible enterprise, motivate our employees' philanthropic work, strengthen relationships with our community, and foster teamwork and values.
Regulatory Update on the Commercial Diagnostic Test Evaluation Process at the Institute of Epidemiological Diagnosis and Reference (INDRE)
The communication issued by INDRE informs about the opening process for requesting the evaluation of commercial diagnostic tests.
Regulatory Update Guide for Modifications to Medical Device Registrations.
The guide provides detailed criteria and requirements for requesting administrative and technical modifications to medical device sanitary registration conditions in Mexico.
Regulatory Update COFEPRIS Proposal Agreement to recognize decisions made by Reference Regulatory Agencies.
The proposal agreement aims to establish provisions for COFEPRIS to utilize and recognize decisions made by Reference Regulatory Authorities and the WHO Prequalification Program for the sanitary registration and life cycle management of health supplies