Our People
Team Leaders from APAC Commercial Regulatory Services

Dr. Sherry Wang

Head of Commercial Regulatory Affairs, SEA and APAC RHQ

Sherry is based in Singapore, leading and overseeing all regulatory efforts and offerings in SEA and APAC regional headquarter (RHQ).

Prior to joining IQVIA, she served as the Assistant Vice President of the commercialization arm in A*STAR. Sherry has more than 20 years of global scientific, clinical and commercial leadership experience in the life sciences industry, as well as an extensive network with key opinion leaders (KOLs) and scientific advisory committees.

From 2008 to 2014, she was an Assistant Professor with the National University of  Singapore, Yong Loo Lin School of Medicine and National University Health System. She maintained as an adjunct before joining industries, where she published more than 50 original high-impact and highly-cited publications in the fields of human cancer and ageing. She also graduated more than 80 university and post-graduate students.

With an established track record of helping some of the leading global healthcare providers achieve market breakthroughs, as well as international acclaim oncology, immunology and ageing-related disease research areas, Sherry is well-positioned to provide strategic inputs across a wide range of offerings, from pre-market regulatory strategies to post-market product license renewals.

Frederick Sim

Pharma Products Lead, Commercial Regulatory Affairs, APAC

Frederick is based in Singapore. He is responsible for providing strategic regulatory advisory and project management for the pharmaceutical and medical device sectors in the APAC region. His expertise covers various aspects, from new product submissions to post-approval lifecycle maintenance and other regulatory compliance activities.

With over 9 years of regulatory affairs experience across various pharmaceutical companies, Frederick has extensive knowledge of APAC markets, including Greater China, South Korea, ANZ, and Southeast Asia. He has played a crucial role in supporting the successful registration and launch of new innovative medicines, generics, and other healthcare products within the region. He has also led and managed multiple regional RA projects with significant business impact across the region.

Jia Ni Chua

Medical Device Lead, Commercial Regulatory Affairs, APAC

Jia Ni is based in Singapore. She is responsible for providing strategic advice on regulatory projects and regulatory intelligence for the medical device and pharmaceutical sectors in the APAC territory. Her responsibilities include handling new product submissions, lifecycle management, and other compliance activities.

Prior to joining IQVIA, Jia Ni had more than 8 years of experience in regulatory affairs roles across various medical device and pharmaceutical companies. During this time, she played a crucial role in supporting the successful registrations and launches of emerging technologies and high-risk medical devices in the Asia Pacific region. Notably, at Medtronic, she was a key member of the international regulatory affairs team in strategizing and securing accelerated registration approvals within APAC.

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