Supplier Qualification
Screening manufacturing partners, DMF/EDMF/USDMF, CEP status and inspection history.
Pharmaceutical supplier qualification for regulated markets
APIs, intermediates, finished dosage forms and CMO support with EU GMP documentation follow-up and transparent China-Europe communication.
Documentation Follow-up
COA, MSDS, GMP documents, change control and technical communication.
Reliable Supply
Support from R&D stage through commercial supply and continuity review.
About Resolution Limited
A China-Europe sourcing partner for regulated pharmaceutical markets
Resolution Limited supports pharmaceutical companies with sourcing, supplier qualification, technical documentation follow-up and project communication across Asian manufacturing networks.
Since its establishment in 2006, Resolution Limited has provided professional sourcing services for pharmaceutical customers in regulated markets.
We focus on practical details that matter to procurement, quality and general management teams: IP protection, NDA-based confidentiality, transparency, qualification status, documentation, continuity and change-control awareness.
Representative offices
offices in Beijing · Hong Kong Tokyo · Melbourne · Dubai Berlin · Montreal & UK
This network supports regional communication, project follow-up and customer coordination when required.
Network references
Selected historical customers and manufacturing network references, where disclosure is permitted.
- Teva
- TAPI
- Mylan
- TOWA
- SHIONO
- UBE
- HISUN
- HENGRUI
- HUAHAI
- JINGXIN
- SPH
- HUAPONT
Product scope
Focused support for pharmaceutical sourcing decisions
Active Pharmaceutical Ingredients
API sourcing with attention to DMF/EDMF/USDMF, CEP status, inspection background and regulated-market documentation.
Intermediates & Raw Materials
Technical and commercial support from R&D stage through scale-up and commercial supply.
Finished Dosage Forms
FDF and contract manufacturing coordination for selected regulated-market requirements.
CMO / Project Support
Supplier communication, sample coordination, documentation follow-up and change-control awareness.
Supplier qualification signals
Manufacturing network with regulated-market experience
Selected manufacturing partners include sites with EU GMP, US FDA inspection history, PMDA approval or inspection experience, CN GMP and other market-specific qualifications where applicable.
Qualification status is verified by product, site and project before disclosure or supply.
- EU GMP
- US FDA
- PMDA
- CN GMP
- DMF/EDMF/USDMF
- CEP / COS
How we work
What customers receive through the sourcing process
You ask
Send the product name, target market and requested quantity if available.
We screen
We review suitable manufacturers, qualification background and supply continuity.
You receive documents
Technical documents, GMP materials and regulatory support files are coordinated.
You confirm
Samples, technical questions, visits and audit preparation can move forward.
You secure supply
Order execution, communication and change-control signals are followed up.
Contact
Start with an inquiry
For an initial inquiry, please send the product name, target market and requested quantity if available. We will first check whether suitable supply options are available. Regulatory documents, samples, timeline and commercial terms can then be discussed step by step.
Resolution Limited
Headquarters office
A1309, CAC Chang'an Center, No. 51 Lugu Road
Shijingshan District, Beijing 100040, China
T: +86 10 6468 7818
F: +86 10 6468 7998
E: info@resolutionpharm.com
offices in Beijing · Hong Kong
Tokyo · Melbourne · Dubai
Berlin · Montreal & UK