Whatever your stage of clinical development, you need a trusted partner providing global regulatory capabilities to support your product. Canny’s consultants understand the importance of delivering sound regulatory strategies and operational support for your products, and provide you with feasible approaches and act as liaison with various regulatory agencies, both on technical and regulatory issues.

By continuously monitoring the global regulatory landscape, and years of submission experiences with NMPA, FDA, EMA, we can advise you across all spectrum of activities and technical functions to stay ahead of any regulatory risks and keep your research on time and budget.