Raymond Ng

Senior Regulatory Affairs Manager at Accestra Consulting

  • Mr. Ng is based in China with almost a decade of regulatory affairs experience of the Chinese market with a Master’s Degree from the University of Nottingham.
  • He has extensive knowledge of Chinese pharmaceutical regulatory requirements and has worked on numerous regulatory submissions with Chinese health authorities.
  • Mr Ng has strong communication and practical experience dealing with the China NMPA (formerly CFDA) and CDE. 
  • A successful track record of supporting the top 50 pharma companies as well as biotech and medtech with market entry into China.
  • To learn more about Raymond or Accestra Consulting, visit their website at www.accestra.com


  • Next: 10-11 Jul 2023 Live online
  • Also: 10-11 Oct 2023 Live online
  • Also: 23-24 Jan 2024 Live online
  • Also: 23-24 Apr 2024 Live online

Understanding Pharmacovigilance Regulations in APAC

New for 2023

Live online

Pharmacovigilance regulations in Asia are dynamic and fast-changing. As the Asia-Pacific region becomes increasingly important for pharmaceutical companies, it's vital to ensure compliance and safety by staying informed of the latest regulatory developments.

  • 6 CPD hours
  • Presented by Helen Ye
  • + 4 more
  • Next: 1 Aug 2023 Live online
  • Also: 1 Feb 2024 Live online

Navigating China’s API Regulations: An Essential Guide to DMF Registration

New for 2023

Live online

Enhance your knowledge of the regulatory requirements for Active Pharmaceutical Ingredients and the Drug Master File in China. An opportunity to learn the quickest pathway options for DMF registration and to hear from industry leaders in this important region.

  • 1.5 CPD hours
  • Presented by Helen Ye
  • and Raymond Ng