FOCAL POINT RESEARCH INC.

Consulting services for the creation, launch and commercialization of consumer products, health care products, beauty care products, cosmetics, drugs, medical devices, natural health products; Regulatory affairs consulting services for consumer products, health care products, beauty care products, cosmetics, drugs with respect to government standards and regulatory compliance, regulatory advice on labeling and advertising; Conflict resolution services, namely, resolving advertising disputes, product shipment and trade disputes for third parties; Testing and market research services, namely, assessment of food and consumer products for consumer acceptability in the areas of taste and feel, analyzing the data produced from consumer research panels to advise clients on the acceptability of their products from the consumer research; Regulatory advice on labeling and advertising; Reviewing labelling and advertising of third parties to assure compliance with government regulations and approval requirements; assuring compliance with language requirements and harmonization of labelling for domestic and foreign efficiency

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 compliance, consumer complaint handling and good manufacturing practices

Quality Assurance assessments, namely, manufacturing quality assessments, prototype quality issues, ingredient analysis, evaluation of finished product specifications; assessment of equipment purchase and quality systems engineering start-up; Clinical trial application and management, namely, preparation and submission of applications to government regulatory bodies and assistance with writing, design and sourcing clinical trials; Environmental compliance consultation, namely, verification and review of product environment claims and data management; Regulatory affairs submissions, namely, preparation of United States FDA submissions, preparation of European Union dossiers; Design and development of computer software for analyzing data submitted by third parties; Regulatory advice on product development, conducting scientific reviews on the safety and efficacy of consumer products; developing and preparing quality standards on these products and preparing government registration and license applications with respect thereto

Regulatory affairs consulting services for medical devices, natural health products with respect to government standards and regulatory compliance