IVD——Regulatory Consultation Service

泰格捷通(北京)医药科技有限公司
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At present, relevant policies and regulations on medical devices change frequently globally and requirements are becoming increasingly stringent, leading the increasing compliance cost. We provide full lifecycle regulatory services on IVD products for the client and promote product compliance. 1. China and global regulatory consultation 2. China and global regulatory training and interpretation 3. Strategy design and assessment 4. Regulatory update