ARTICLE
19 August 2021

Mexico Amends The Health Law Regulations With Impact In The Approval Of Medicines

O
OLIVARES

Contributor

Our mission is to provide innovative solutions and highly specialized legal advice for clients facing the most complicated legal and business challenges in Mexico. OLIVARES is continuously at the forefront of new practice areas concerning copyright, litigation, regulatory, anti-counterfeiting, plant varieties, domain names, digital rights, and internet-related matters, and the firm has been responsible for precedent-setting decisions in patents, copyrights, and trademarks. Our firm is committed to developing the strongest group of legal professionals to manage the level of complexity and interdisciplinary orientation that clients require. During the first decade of the 21st century, the team successfully led efforts to reshape IP laws and change regulatory authorizations procedures in Mexico, not only through thought leadership and lobbying efforts, but the firm has also won several landmark and precedent-setting cases at the Mexican Federal and Supreme Courts levels, including in constitutional matters.
Last May 31, 2021, the Ministry of Health issued a decree in the Official Gazette, amending several articles of the Health Law Regulations.
Mexico Food, Drugs, Healthcare, Life Sciences
To print this article, all you need is to be registered or login on Mondaq.com.

Last May 31, 2021, the Ministry of Health issued a decree in the Official Gazette, amending several articles of the Health Law Regulations. The most relevant points of this decree were the following:

  • COFEPRIS allows the submission of documentation in English, without translation into Spanish within sanitary approval applications. In the case of documents issued by a foreign Authority, they must be legalized.
  • The labels of products destined for the public sector must now be differentiated from those of the private.
  • For the approval of biocomparable medicines, the participation of the Subcommittee for the Evaluation of Biotechnological Products was eliminated, now it is sufficient the New Molecules Committee opinion.
  • Clinical studies in the country of origin of biocomparable medicines can be submitted as evidence for the Marketing Authorization application. When applying for a renewal of the Marketing Authorization, clinical studies in Mexico must be submitted.
  • The first extension must be requested 5 years after the approval and must be resolved within 120 days.
  • To obtain the first Marketing Authorization renewal, all products will be monitored by the regulatory agency, taking into account the effects of the product during its first years in the market.
  • For further renewals must be requested/ informed to COFEPRIS every five years, and no later than 150 calendar days before the expiration of the Marketing Authorization.
  • The statutory terms regarding applications to modify the Marketing Authorization have changed, the regulatory agency shall issue a response within 45 days for technical modifications and 20 days for administrative modifications.
  • If the modification of the Marketing Authorization is authorized, the holder will have a period up to 240 calendar days to eliminate the stock of the product.

These amendments to the Health Law Regulation, in general, are focused on improving the analysis and resolution of various processes.

OLIVARES will continue to analyze the impacts of these changes in order to guide our clients and the industry with best practice strategies.

Originally published 8 June 2021.

The content of this article is intended to provide a general guide to the subject matter. Specialist advice should be sought about your specific circumstances.

We operate a free-to-view policy, asking only that you register in order to read all of our content. Please login or register to view the rest of this article.

ARTICLE
19 August 2021

Mexico Amends The Health Law Regulations With Impact In The Approval Of Medicines

Mexico Food, Drugs, Healthcare, Life Sciences

Contributor

Our mission is to provide innovative solutions and highly specialized legal advice for clients facing the most complicated legal and business challenges in Mexico. OLIVARES is continuously at the forefront of new practice areas concerning copyright, litigation, regulatory, anti-counterfeiting, plant varieties, domain names, digital rights, and internet-related matters, and the firm has been responsible for precedent-setting decisions in patents, copyrights, and trademarks. Our firm is committed to developing the strongest group of legal professionals to manage the level of complexity and interdisciplinary orientation that clients require. During the first decade of the 21st century, the team successfully led efforts to reshape IP laws and change regulatory authorizations procedures in Mexico, not only through thought leadership and lobbying efforts, but the firm has also won several landmark and precedent-setting cases at the Mexican Federal and Supreme Courts levels, including in constitutional matters.
See More Popular Content From

Mondaq uses cookies on this website. By using our website you agree to our use of cookies as set out in our Privacy Policy.

Learn More