STRATEGIC BUSINESS DEVELOPMENT
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How to use the US supplement, OTC and food and beverage market as a benchmark? What are the trends? Can your product be successful in North America? What are the steps necessary for US market entry? What is the best regulatory path? Are you a dietary supplement, functional food, homeopathic or a new dietary ingredient?
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Navigating the regulatory environment in the US: How do the US regulations apply to you and your product?
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Dietary Supplement Health and Education Act of 1994 (DSHEA)
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Public Health Security and Bioterrorism Preparedness and Response Act of 2002
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Agriculture Improvement Act of 2018 (AKA the Farm Bill)
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Federal Food, Drug, and Cosmetic Act and subsequent amending statutes are codified into Title 21
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Strategic intellectual property review, evaluation, white space identification and licensing
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Scientific, targeted basic science and clinical research that supports company objectives and protects investments
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Identification of proprietary ingredients from all over the world and potential licensing opportunities in your market
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Examples of other landmark products and brands from other markets
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Strong background for regulatory, quality and manufacturing for drugs, supplements, dermo-cosmetics and foods
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GMPs for drug, food, supplements and cosmetics in US, EU, Canada, Japan, Mexico and China (regs are changing every day).