Seventeen years sourcing the raw materials other people formulate with
Bioran Pharma Co., Ltd. is a pharmaceutical raw-material supplier working with generic manufacturers, CDMOs and qualified distributors. We do not own a single reactor. What we own is the qualification work between the site and your QA department.
What we actually do
A trading company with a quality department, and we are explicit about that
Most suppliers in this category describe themselves as manufacturers. We are not one. We work with six audited GMP sites, hold the commercial relationship, and take responsibility for the documentation, the release specification and the response when a batch is questioned.
That model has a real advantage: we can move a product between sites when a route, capacity or regulatory situation changes, instead of asking you to re-qualify a single plant. It also has a real limitation: if you require a dedicated manufacturing site with your name in the site master file, we are the wrong supplier and we will tell you so.
What we will not do is put a facility photograph on a website that is not ours, or quote a certification we do not hold for a product. Buyers in this industry check, and being caught once ends the account.
- Legal entity
- Bioran Pharma Co., Ltd.
- Founded
- 2009
- Product lines
- APIs · intermediates · veterinary · packaging
- Catalogue
- 67 documented products online
- Audited sites
- 6 (GMP, beta-lactam segregated)
- Markets
- 42 countries, 5 regions
- Registered address
- 18F, No.1 Building, No.487 Yangmuqi Road, 315042 Ningbo, China
- Business hours
- Mon–Fri 08:30–18:00 (GMT+8) · Technical desk answers within one business day
Capabilities
What you can actually buy from us
Four capabilities, each with a limit worth knowing before you send an enquiry.
Multi-site manufacturing
Six audited GMP sites across China supplying APIs, intermediates and veterinary actives, with beta-lactam and non-beta-lactam production segregated.
Custom synthesis
Route scouting, scale-up and campaign production from kilogramme to multi-tonne, with the route and impurity profile disclosed to your specification.
Documentation ownership
A regulatory affairs team that maintains DMFs, CEPs and change-control notifications — and says no when a document does not exist.
Export logistics
Consolidated shipping with temperature, humidity and dangerous-goods handling, plus destination-market labelling on request.
Desk-audit paperwork and export palletisation — the two layers of the service you can verify before you travel anywhere.
Markets
Where the goods are released decides the paperwork
We prepare the regulatory file for the market of release. Below is what that means in practice for each region we serve regularly.
- EuropeCEP & EU-GMP documentation, EDQM-aligned dossiers
- North AmericaUSDMF Type IV support, cGMP audit packs
- Latin AmericaANVISA / COFEPRIS registration assistance
- South & Southeast AsiaBulk supply with local release testing
- Middle East & AfricaTender-ready packs, Arabic labelling
Want to see whether we can support your filing?
Send the product, the market and the registration route. You will get an honest yes, no, or 'not yet' — in writing, within two business days.