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.
常州乾虹生化製薬有限公司-循環器系薬、消化器系薬、抗腫瘍薬、脂質低下薬、循環器系薬、血液系薬、原料
常州乾虹生化学製薬有限公司（株式略称：Qianhong Pharmaceutical、証券コード：002550）は、2008 年 3 月 15 日に設立されました。その前身は 1971 年に設立された常州生化学工場です。2011 年 2 月 18 日に深セン証券取引所の中型取締役会に上場されました。
- 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
- 医薬品製造
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 医薬品製造: 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.