TH,INC.

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Description

THinc is a pharmaceutical consulting company committed to building successful partnerships with our clients by providing an integrative approach to regulatory affairs, medical writing, and toxicology throughout the drug-development process. THinc’s track record of success includes 17 New Drug Applications (NDAs), 5 in the Common Technical Document (CTD) format, and strategic regulatory and nonclinical guidance in at least 30 new chemical entity (NCE) development programs. THinc is located in the heart of the biotechnology industry in the San Francisco Bay Area. Since its inception in 1995, THinc has continued to offer a combination of in-depth knowledge and operational skills to our clientele who range from start-up to Fortune 500 companies. For all our clients, THinc has the flexibility to handle a quick turnaround project or act as a virtual regulatory affairs, medical writing, or toxicology department. Our regulatory affairs professionals are well-positioned to advise and collaborate with clients on drug-development strategies in the areas of clinical, nonclinical, and chemistry, manufacturing, and controls (CMC). By helping clients to strategize, develop, and formulate solutions to regulatory issues as well as to compile submissions that are compliant with regulatory guidelines, we offer a full-service regulatory department.

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