Practice Areas
Mandi provides both advisory and litigation support to her life sciences and health care sector clients. She advises pharmaceutical and medical device companies across a range of regulatory compliance and investigations matters, including compliance with therapeutic goods legislation and associated regulations and codes, Therapeutic Goods Act (TGA) audits, product registrations and listings, advertising and labelling, competitor complaints, crisis management and communications, contractual disputes, product liability claims, disciplinary proceedings, product recalls and recall strategies, defective or unsafe therapeutic goods, import and export requirements, quarantine laws, as well as data and privacy issues.
Mandi also advises pharmaceutical and medical device companies on contract negotiations with government agencies and hospitals, including drafting supply and consignment agreements.
Mandi also prepares internal policies for compliance with privacy and social media.