Enabling Innovative Drug Discovery with Advanced Technologies
The Regulatory Affairs team has significant experience in drug development and establishment of regulatory strategies. This endows our clients to develop their new drugs more efficiently and to accomplish timely and successful regulatory submissions.
Key Offerings Include:
Dossier/submission preparation or review and filing
Development of regulatory strategy for the product's life cycle
Facilitate interaction with regulatory agencies, such as in meetings and conference calls, negotiations during development stages, submissions and submission approval process.
HitGen Inc.
Building C2, NO.8, Huigu 1st East Road
Tianfu International Bio-Town,
Shuangliu District, Chengdu City,
Sichuan Province,P.R. China
Tel : +86-28-8519-7385
HitGen Pharmaceuticals Inc.(US Subsidiary)
Tel : +1-(508)-840-9646
Vernalis (R&D) Limited (UK Subsidiary)
Granta Park,Great Abington
Cambridge,CB21 6GB
United Kingdom
Tel : +44(0)1223-895555
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