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.

Submission Services

Our submission services professionals possess a wealth of experience in preparing electronic and paper submissions, and in participating as a team member on our clients project teams.

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NEWSREEL - What's New at THinc

NEW SERVICE - THinc now offers full submission services. Let us help you to prepare for May 2018! 
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