The core members of BrilliantMed come from top 500 MNC companies, including Bayer, Novo Nordisk, Sanofi, etc. Each member has more than 15 years of work experience in the pharmaceutical industry, with rich professional knowledge and skills.
Strategic Consulting on Pharmaceutical and Health Product Registration in Key Regions of China, the United States, Europe, and the Asia-Pacific.
Help enterprises build a registration affairs operation system, optimize related processes, and formulate SOPs.
Professional registration documents, GxP compliance review services, compliance training
High-efficiency, precise, compliant, and globally-covered eCTD publishing and submission services, including the construction and training of related systems.

Beijing BrilliantMed Pharmaceutical Technology Co., Ltd. (hereinafter referred to as BrilliantMed Pharmaceutical) was established in 2024 and is registered in Beijing, China. The company's main business direction is to provide high-quality global registration consulting and registration management operation services.
The core members of BrilliantMed Pharmaceutical come from Fortune 500 companies, including Bayer, Novo Nordisk, Sanofi, etc. Each member has more than 15 years of work experience in the pharmaceutical industry and possesses rich professional knowledge and skills.
Currently, our services mainly include formulating global registration strategies, executing local registration submissions, and publishing electronic submission documents on a global scale. We are committed to helping our clients understand the regulatory requirements of different regions, ensuring that various registration applications of their products can be submitted in a timely and accurate manner worldwide, so as to complete their global market layout.
Upholding the service concept of "integrity as the foundation and professionalism as the paramount", we continuously innovate and optimize our service processes to provide our clients with comprehensive and professional solutions. In an increasingly stringent regulatory environment, we are committed to providing efficient and compliant electronic submission services, and have won widespread recognition and trust within the industry.
Looking ahead, we will continue to strengthen technological innovation and service upgrades, promote the healthy development of the pharmaceutical industry, and create greater value for our clients. We look forward to cooperating with clients around the world to create brilliance together.
Currently, our services mainly include formulating global registration strategies, executing local registration submissions, and publishing electronic submission documents on a global scale.
China-US Dual Submissions·RA Fast Track
Strategist × Project Manager × Publishing Expert
Global Registration · Local Direct
Full coverage of the United States, Europe, Asia-Pacific regions, with no worries about the last mile.
eCTD Global Master · Faster and Higher Cost-Effectiveness
One set of system manages globally, enabling submissions in multiple countries with zero time difference.
A small tool solves a big problem
Are you still driven crazy by daily repetitive work?Contact us, and we will customize a time-saving and labor-saving automated mini-program specifically for you...We are committed to helping our clients understand the regulatory requirements of different regions, ensuring that their products can be submitted for various registration applications in a timely and accurate manner on a global scale, so as to complete their global market layout.
Looking ahead, we will continue to strengthen technological innovation and service upgrading, promote the healthy development of the pharmaceutical industry, and create greater value for customers. We look forward to cooperating with global customers to create brilliance together.
Room 508, Building 8, Zhongke E-commerce Valley, No. 20 Guangde Street, Beijing Economic and Technological Development Area, Beijing City
+86 15001236015
Sophia.huang@brilliantmed.cn