Sonia Nath

Practice Areas

Sonia has deep experience in matters involving the Food and Drug Administration (FDA). Her practice encompasses investigations, litigation and regulatory counseling, as well as advising on transactional matters. Sonia routinely counsels clients on FDA regulatory compliance matters, including developing go-to-market strategies for companies – particularly in the medical device space – and representing companies at pre-submission meetings; reviewing labeling, advertising and promotional materials for drugs, devices, biological products, food and dietary supplements; and working hand-in-hand with business leaders to ensure the chosen regulatory pathways align with overall business strategy, including plans for developing and protecting intellectual property. Sonia has experience working across all FDA-regulated product areas, with a particular emphasis on the biotech and medtech industries.

The transactional side to Sonia’s practice involves advising investors, underwriters, and public and private businesses in buy-side and sell-side transactions, as well as in financings involving FDA-regulated products.

Career

Sonia served for almost 12 years at the FDA’s Office of the Chief Counsel as a litigation and enforcement attorney, Sonia helps clients prepare for and respond to interactions with the FDA, including FDA enforcement actions, Warning Letters and inspections. Sonia’s practice also focuses on conducting internal investigations and representing clients in criminal matters involving the FDA and FDA-regulated products. She also advises and represents clients in civil litigation involving FDA regulatory issues.

During her FDA tenure, Sonia gained subject matter experience across the gamut of FDA-regulated products, including prescription and over-the-counter drugs, medical devices, biologics, foods, cosmetics, dietary supplements and animal drugs. Sonia negotiated dozens of civil consent decrees for the government, defended the FDA in lawsuits brought under the Administrative Procedure Act and the Freedom of Information Act and handled False Claims Act litigation for the agency. Sonia also handled criminal investigations and prosecutions involving FDA-regulated products in her appointed role as a Special Assistant United States Attorney (SAUSA) with the US Attorney’s Office for the Central District of California.

Sonia received numerous accolades for her government service – including the FDA’s Award of Merit (the agency’s highest recognition), the FDA Commissioner’s Award and the Department of Justice’s John Marshall Award (the DOJ’s highest award offered to attorneys).