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Company Introduction

China is home to one of the largest pharmaceutical markets in the world offering access to vast patient populations with an increasingly westernized incidence of disease. For manufacturers of pharmaceuticals, biologics and certain medical devices looking to enter China, the China Food and Drug Administration (CFDA) requires the conduct of clinical trials to support market applications. In addition, China is also becoming an increasingly more attractive location to support Regional and Global product development. With the CFDA making a conscious effort to improve the regulatory environment as well as industry quality standards in general, China has seen a large influx of clinical studies from Sponsors all over the world spanning all kinds of Therapeutic Areas.

The opportunities for drug and device manufacturers in China are matched only by the challenges that are also unique to China. That’s why it’s of growing importance to work with a CRO that is local to the area, that understands how to navigate through the obstacles and take full advantage of the opportunities.

You need to find a CRO that can:

  • Promise top quality deliverables, every time
  • Expedite timelines
  • Provide you with innovative and cost-effective solutions

In order to do so in China your partner must:

  • Have a strong track record for high quality deliverables and services
  • Have extensive knowledge of the local clinical trial environment, from regulations through to Sites and KOL.
  • Have formed great working relationships with local Sites and KOL through years of experience conducting clinical trials across the whole country

This is who we are, this is what we do.

If you would like to learn more about R&G, please download our brochure or feel free to contact us directly.

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