Our health law practice involves advising on every aspect of a regulated business including:

• clinical trial agreements and commercial agreements with wholesalers, distributors, retail pharmacies and other third parties;
• regulatory submissions for approval to Health Canada;
• pre-Notice of Compliance materials for healthcare professionals, product launches, post-approval marketing materials (including detail aids, physician restricted websites, disease state material, and television/radio/ print advertising) and compliance with product labeling laws;
• responses to buying group and hospital requests for proposals (“RFPs”);
• Patented Medicine Prices Review Board (PMPRB),formulary reimbursement and product listing agreements;
• complaints relating to compliance with the Food & Drugs Act, Competition Act, Pharmaceutical Advertising Advisory Board Code of Advertising Acceptance, Rx&D Code of Ethical Practices, MEDEC DiabetesImplementation Guidelines and internal company codes;
• product recalls for pharmaceuticals, medical devices, cosmetics and consumer products;
• conducting healthcare and anti-corruption compliance investigations;
• privacy and health information law and compliance;
• federal and provincial access to information laws and government relations; and
• in-house training on all aspects of compliance including healthcare, anti-corruption/anti-bribery, competition law, marketing & advertising and contract risk management.