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.
Changzhou Qianhong Biochemical Pharmaceutical Co., Ltd.-순환기약, 소화기약, 항종양약, 지질강하제, 심혈관 및 혈액계약, 원료
Changzhou Qianhong Biochemical Pharmaceutical Co., Ltd.(주식 약어: Qianhong Pharmaceutical, 주식 코드: 002550)는 2008년 3월 15일에 설립되었습니다. 그 전신은 1971년에 설립된 Changzhou Biochemical Factory였습니다. 2011년 2월 18일에 선전 증권 거래소 중소기업 이사회에 상장되었습니다.
- 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
- 의약품 제조
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 의약품 제조: 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.