Regulatory Affairs

Our regulatory affairs professionals are well-positioned to advise and collaborate with clients on drug-development strategies and execution in the areas of clinical, nonclinical, and chemistry, manufacturing, and controls (CMC).

Regulatory and Medical Writing

Our medical and scientific writers have extensive experience in producing on-time, high-quality regulatory documents to support drug-development programs from pre-IND through Phase 4.

Nonclinical Safety

Our nonclinical safety professionals possess a wealth of experience in planning, analysis, and interpretation of nonclinical studies and in integrating the nonclinical findings into the clinical program.

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NEWSREEL - What's New at THinc

NEW SERVICE - THinc now offers monitoring and management of clinical trial study sites and CROs.  
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Recent assignments and presentations in FY 2012-Strategy, Regulatory Documents, Interactions with Agencies, Scientific Communication, Clinical Operations, Regulatory Operations, and more!
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