Changzhou Qianhong Bio, pharma Co., Ltd.
Company-provided description, not an official-source fact. Certifications, capacities, years and market positions stated in it are the company's own claims until a record below confirms them.
Công ty TNHH Dược phẩm Sinh hóa Thường Châu Qianhong-Thuốc hệ tuần hoàn, thuốc hệ tiêu hóa, thuốc chống khối u, thuốc hạ lipid máu, thuốc tim mạch và hệ máu, nguyên liệu
Công ty TNHH Dược phẩm Sinh hóa Thường Châu Qianhong (tên viết tắt: Qianhong Pharmaceutical, mã chứng khoán: 002550) được thành lập vào ngày 15 tháng 3 năm 2008. Tiền thân của nó là Nhà máy Hóa sinh Thường Châu được thành lập vào năm 1971. Nó được niêm yết trên Hội đồng quản trị vừa và nhỏ của Sở giao dịch chứng khoán Thâm Quyến vào ngày 18 tháng 2 năm 2011.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Changzhou, China
- Website
- https://www.qhsh.com.cn
- Categories
- Sản xuất dược phẩm
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 3 official records from 3 official sources are on file. Everything is listed below with its evidence type: each entry confirms only what it literally says; none of them is a review. The manufacturing role above rests on the official records listed below, and only as far as each literally goes: a facility registration or licence is not an observation of current production. Nothing here confirms ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Market access approved: European Union (record type: market-access-eu; this record does not by itself establish manufacturing) [official record; status green] Shows the facility is on the destination market's list of establishments approved for the listed goods. A listing is not an observation of current production. checked 2026-08-22. TRACES NT, European Commission register of approved establishments (DG SANTE)
- GMP certificate from a medicines agency (record type: gmp-certified; this record does not by itself establish manufacturing) [official record; status green] A medicines regulator inspected the site and confirmed it may manufacture medicines. checked 2026-10-03. ANVISA (Brazilian Health Regulatory Agency), public register of Good Manufacturing Practice certificates (CBPF)
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-10-03. Agencia Estatal de Medicamentos y Tecnologias en Salud (AGEMED, Bolivia), listado oficial de registros sanitarios aprobados
Import rules for these goods
Product-specific import rules not established for the catalog category Sản xuất dược phẩm: neither the company's own description nor an official activity code shows that its own goods are of this kind. A catalog category alone is our classification, not proof of what the company makes or sells.
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.