The Preferred Supplier program is about quality and confidence in the supply chain from start to finish. In order to display the Preferred Supplier seal, participating companies satisfy stringent acceptance criteria each year to ensure ongoing compliance. If they are a Preferred Supplier, you can trust they’ve taken the critical steps necessary to display the seal.
About Amin Talati Upadhye LLP
Amin Talati Upadhye LLP is focused on the industries of food and beverages, nutritional supplements, cosmetics and pharmaceuticals. We provide full legal services for the lifecycle of products aimed at improving the population’s health and wellness.
Amin Talati Upadhye has gained a strong reputation for its work at the cutting edge of food, drug (FDA), advertising (FTC) and intellectual property (IP) laws, responding nimbly to rapid changes in the regulatory climate and market place. We work with some of the most innovative products in this sphere, such as raw juices, allergy-free foods, botanical drugs, cosmeceuticals and hemp products. We counsel on regulatory compliance and risk-analysis, product development, as well as on trademark and patent protection.
In addition to guiding our clients through the strategic development of new products through regulatory approvals to the marketplace, we advise on all post-launch processes as well to ensure labeling, advertising, safety and manufacturing compliance requirements. We counsel on recalls, consumer false advertising class actions, trademark and patent infringement disputes, FDA, FTC and State AG government investigations, commercial (breach of contract) litigation, unfair competition, Proposition 65, National Advertising Division and Consumer Product Safety Commission matters. We also provide IP and compliance due diligence assessments in mergers/acquisitions and guide companies on IP freedom-to-operate opinions.
Our attorneys also work closely with pharmaceutical companies through the entire development pipeline, from prototype development and clinical trials with an eye towards gaining FDA approval, through eventual patent applications and possible infringement challenges in court. We have developed a special renown in the representation of generic drug companies in Paragraph IV litigation: the process whereby companies challenge patents held by brand name companies in order to bring these important, often life-saving, medications to the market in generic forms.
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