Combining deep expertise in life sciences regulatory law with experience across the pharmaceutical, biotech, and medical device sectors, Baker McKenzie‘s team advises on domestic and multijurisdictional M&A transactions, restructuring projects, and commercial matters. The team also advises on licensing for manufacturing, sales, distribution, and advertising, while supporting clients on compliance and anti-corruption matters, product liability and safety disputes, consumer protection, and IP, including healthcare-related trade marks. Practice head Vanina Caniza, the firm’s global chair of healthcare and life sciences, advises multinational, regional, and Argentine clients on compliance, commercial agreements, M&A, and regulatory matters across pharmaceuticals, biotech, and medical devices. Santiago Maqueda, a specialist in regulatory assessments and dispute resolution, frequently advises clients on contracts with government entities, partners, and suppliers. Also part of the core team, senior associate Rocío Rojas Iglesias handles transactional and regulatory matters involving the healthcare and life sciences sectors.

Marval O’Farrell Mairal's market-leading life sciences and healthcare practice advises major clients across biopharmaceuticals, healthcare, health-tech, medical devices, cosmetics, food, animal health, agribusiness, and chemicals on regulatory, transactional and compliance matters. Highlighted for his 'deep and comprehensive knowledge of the regulatory landscape in Argentina and key Latin American markets', practice head Martín Mosteirin has over 20 years of experience advising global companies on regulatory issues, cross-border transactions, contentious matters, product liability, product recalls, and commercial contracts. Other noteworthy practitioners include Camila Leone, who regularly assists pharmaceutical and healthcare companies with business restructuring, disputes and regulatory procedures, and Carolina Andrea Ramírez, a name to note for global companies seeking advice on regulatory compliance, transactions and contentious matters.

Allende & Brea advises major domestic and international clients in the pharmaceutical, medical devices, and food industries on a wide range of matters, from incorporation and registration with state health authorities to M&A, joint ventures, reorganisations, and commercial agreements, such as manufacturing, licensing, and distribution contracts. It also supports clients with regulatory compliance, data privacy, and dispute resolution, including administrative proceedings before food and drug authorities. Following the mid-2025 departure of former co-head María Morena del Río, the practice is currently solely led by Fernando Martínez Zuviría, who focuses on supporting laboratories and medical device manufacturers with transactional, corporate, contractual, and regulatory matters. The team’s expertise is further strengthened by Vanesa Fernández, who specialises in life sciences administrative and regulatory issues, and Lucrecia Re, who represents pharmaceutical and medical device companies in regulatory and administrative proceedings.

Praised for 'its extraordinary level of specialisation in industry regulation and global compliance', Beccar Varela advises clients across the pharmaceutical products, medical devices, cosmetics, digital health, and healthcare services sectors, providing support on transactions, IP, contentious matters, and regulatory issues. The team also works in specialised areas such as orphan products, the exception access regime for pharmaceutical products, medicinal cannabis, and clinical trials, and has recently expanded its work to include telemedicine, electronic prescriptions, and electronic pharmacies. The practice is led by Ana Andrés, who has over a decade of experience advising local and international life sciences clients on regulatory, corporate, and litigation matters. She is supported by Luciana Malito and Cruz Ignacio Uranga, both of whom focus on transactional and corporate mandates.

The life sciences and healthcare practice at Bomchil combines regulatory and litigation expertise to handle contractual and regulatory matters in areas such as health protocols, tobacco-free products, and clinical practice guidelines, including obstetrics and surrogate motherhood liability. The team also advises on medical malpractice cases, clinical trials, and telemedicine, representing a broad range of healthcare and life sciences clients across Argentina. The practice is led by Melisa Romero, who has substantial experience in contractual and regulatory matters, data protection, dispute prevention for healthcare clients, and medical professional liability proceedings. At the associate level, María Victoria Casale handles healthcare regulatory matters and obstetrics and neonatology malpractice cases, acting for private health providers.

With experience across the pharmaceutical, healthcare, cosmetic, food and beverage, agribusiness, biotechnology, and medical devices sectors, Bruchou & Funes de Rioja's life sciences and healthcare practice handles a wide range of matters, including commercial agreements, M&A, regulatory and compliance matters, dispute resolution, and IP. The practice is jointly led by Estanislao Olmos, who specialises in life sciences M&A, distribution agreements, and regulatory matters, and Dámaso Pardo, whose experience covers IP, trade agreements, as well as pharmaceutical, medical device and biotechnology patents. Other key practitioners include administrative and regulatory law specialist Juan Zocca, who assists pharmaceutical, healthcare and biotech companies on ANMAT registrations, medicinal cannabis regulations, and compliance with chemical precursor laws, and Gabriel Lozano, whose main strength lies in M&A and competition matters.