ARTICLE
4 September 2020

In Mexico, COFEPRIS Announces New Rules For The Authorization Of Generic Drugs

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.
COFEPRIS will have a special procedures window for the generic pharmaceutical products.
Mexico Intellectual Property

On August 19, 2020, the regulatory agency in Mexico (COFEPRIS), which as we have indicated in a previous newsletter, will soon be incorporated into the Ministry of Health, losing its status as an autonomous entity, announced new operating rules for the approval of generic drugs in Mexico, based on the following guidelines:

  • COFEPRIS will have a special procedures window for the generic pharmaceutical products.
  • These applications for approvals of generics could be filed, the day after the granting of the patent related to the innovative medicine.
  • The respective applications would be decided at any time, prior to the expiration of the patent, if the registration or approval is given, COFEPRIS will provide a provisional official communication, which would be exchanged for the definitive sanitary registration or approval, the day after the expiration or the validity of the patent.

COFEPRIS indicates that they are complying with the elimination of the temporality of 3 years (for chemically synthesized drugs) and 8 years (for biotechnological) to research and develop generics or biocomparables, according to the reforms to the so-called Bolar Exception in the new Federal Law for the Protection of Industrial Property (New IP Law) which will enter in force by November 2020.

The communication also mentions that the rules for granting sanitary registrations of generic drugs, "second-use patents, which refer to the therapeutic indication, are no longer allowed," which seems to mean that the patents of new uses will not be considered as part of the linkage system.

We consider that these rules announced by COFEPRIS, are only a statement on its official website, still without legal basis. Likewise, it represents a statement contrary to the patent system, the patent linkage system, the Mexican Constitution and international treaties. It will be necessary to analyze the complete and legal contents and their scope to confirm, if these rules indeed contradict the law.

OLIVARES is monitoring the implementation of these rules and analyzing the scope of the content of this communication.

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.

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