Class 044
Medical, Beauty & Agricultural Services
Consulting services for the creation, launch and commercialization of consumer products, health care products, beauty care products, cosmetics, drugs, medical devices, natural health products and food (2) Regulatory affairs consulting services for consumer products, health care products, beauty care products, cosmetics, drugs, medical devices, natural health products and food with respect to government standards and regulatory compliance, regulatory advice on labeling and advertising, regulatory advice on product development, conducting scientific reviews on the safety and efficacy of these types of products, developing and preparing quality standards on these products and preparing government registration and license applications with respect thereto (3) Reviewing labelling and advertising of third parties to assure compliance with government regulations and approval requirements; filing submission and corresponding with government regulatory bodies; (4) Conflict resolution services, namely, product shipment and trade disputes for third parties (5) Training services, namely training personnel of companies whose businesses involve cosmetics, drugs, natural health products, consumer products, and medical devices in the field of quality assurance, ISO quality management system compliance, consumer complaint handling and good manufacturing practices. (6) Quality Assurance and Good Manufacturing Practices (GMP) assessments, namely import and export requirements, manufacturing activities quality assessments, prototype quality issues, ingredient analysis, evaluation of finished product specifications; assessment of equipment purchase and quality systems engineering start-up, quality assurance review and auditing services for manufacturers, packagers, labellers and importers of health products (7) Clinical trial application and management, namely preparation and submission of applications to government regulatory bodies and assistance with scientific research, literature review, technical, design and sourcing clinical trials; (8) Environmental compliance consultation, namely verification and review of product environment claims and data management (9) Regulatory affairs submissions, namely preparation of Health Canada and United States FDA submissions, preparation of European Union dossiers
