“In my twenty years of Class III medical device experience, I have not had the pleasure of working with a Chinese regulatory firm as talented and knowledgeable.As CFDA is increasing their technical and clinical review, it is one of the few companies staffed to assist medical device companies in this area. Their focus and dedicated support has exceeded out expectation. In my search for a strategic partner in China, they exceeded the other companies in all areas. While they have a very experienced Regulatory and Marketing team, their technical engineering, clinical, and international project management expertise place them above other companies in this area.”
Vice-President,Global Regulatory/Clinical AffairsImplantable Device“在我过去20年的三类医疗器械从业经验中，并未找到令人满意的中国法务咨询公司。由于CFDA不断提高技术和临床审查要求，贝迪诺恩是少数几个能提供专业咨询的公司之一。贝迪诺恩的从业专注度及客户支持度超出我们的预期。在我寻找中国战略合作伙伴的过程中，发现他们具备经验丰富的注册和市场团队，拥有技术、临床和国际项目管理的专业知识及经验，他们完全超越该领域的其他公司。”
国际植入医疗器械生产商副总裁，国际注册/临床事务部