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Global Registration Strategy
Local Registration Service
Registration Process Opitimization and Operational
Registration Compliance Review
Efficient Publishing of eCTD Dossier
Innovation Consulting
China-US Dual Submissions·RA Fast Track
Global Registration · Local Direct
eCTD Global Master · Faster and Higher Cost-Effect
A small tool solves a big problem
eCTD
Interpretation of the eCTD Technical Guidelines
Deploying eCTD-related systems within the company
eCTD process optimization and SOP development
eCTD Professional Technical Training
eCTD end to end service and partical outsourcing s
A small tool solves a big problem.
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Global Registration Strategy Expert
EU Clinical Trial Regulation and CTIS System Exper
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Introduction to the Business
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Introduction to the Business
Regulatory Services for Pharmaceutical and Health Products2025-03-12
Strategic Consulting on Pharmaceutical and Health Product Registration in Key Regions of China, the United States, Europe, and the Asia-Pacific.
Regitration Process Opitimization and Operational Management2023-12-27
Help enterprises build a registration affairs operation system, optimize related processes, and formulate SOPs.
Registration Compliance Review2023-12-27
Professional registration documents, GxP compliance review services, compliance training
Efficient Publishing of eCTD Dossier2023-12-27
High-efficiency, precise, compliant, and globally-covered eCTD publishing and submission services, including the construction and training of related systems.
Contact

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
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