About 2 Trademarks found for “Focal Point Research Inc.”

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; Testing services, namely assessment of food and consumer products for consumer acceptability in the areas of taste and feel; Design and development of computer software for analyzing data submitted by third parties.

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, 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; 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; Conflict resolution services, namely resolving advertising disputes, product shipment and trade disputes for third parties; Regulatory affairs consulting services for medical devices, natural health products 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; Regulatory affairs submissions, namely preparation of United States FDA submissions, preparation of European Union dossiers.

Providing quality assessment services; 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; preparation of scientific reports; conducting scientific reviews on the safety and efficacy of consumer products, health care products, beauty care products, cosmetics, drugs, medical devices, natural health products and preparing government registration and license applications with respect thereto; developing and preparing quality standards on consumer products, health care products, beauty care products, cosmetics, drugs, medical devices, natural health products and preparing government registration and license applications with respect thereto; clinical trials; clinical trial application and management, namely preparation and submission of applications to government regulatory bodies and assistance with writing, design and sourcing clinical trials; consultancy services relating to environmental compliance; environmental compliance consultation, namely verification and review of product environment claims and data management; design and development of computer software; design and development of computer software for analyzing data submitted by third parties.

Consultancy services relating to healthcare [medical], beauty care and cosmetics.

Advisory and consultancy services relating to regulatory affairs; 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; 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; regulatory affairs consulting services for medical devices, natural health products 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; regulatory affairs submissions, namely preparation of United States FDA submissions, preparation of European Union dossiers; 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; clinical trial application and management, namely preparation and submission of applications to government regulatory bodies and assistance with writing, design and sourcing clinical trials; conflict resolution services; conflict resolution services, namely resolving advertising disputes, product shipment and trade disputes for third parties.