Advice regarding regulation (including Mexican Official Standards (NOM) or Mexican Standards (NMX)), contracting, internal auditing, and implications on M&A processes regarding pharmaceutical products and related substances; restricted substances; medical devices (including nuclear safeguards); products posing health risks for humans, animals, or plants; food and beverages; dietary supplements; cosmetic products; tobacco products; and alcoholic beverages.
Advice on requirements for manufacturing, supply, distribution, marketing, importation, and advertising of products subject to health requirements and acquisition of permits, authorizations, notices, and registrations before health authorities.
Advice on prohibited acts in sales of pharmaceuticals, medical devices, and other products by government related doctors or other health personnel.
Advice on clinical trials and research related to human advice on animal health.
Representation in litigation related to pharmaceuticals, medical devices, food and beverages, tobacco, and cosmetics.
Lobbying and negotiation with authorities regarding amendments or changes to applicable provisions.
Advice on requirements regarding animal processing premises including federal standard slaughterhouses.
Drafting and negotiation of agreements for industries subject to regulatory compliance including: raw material processing, manufacturing, hosting, supply, licensing, marketing, and distribution.
