Reyoung Pharmaceutical 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.
रुईयांग फार्मास्युटिकल कंपनी लिमिटेड एक व्यापक आधुनिक फार्मास्युटिकल कंपनी है जो अनुसंधान एवं विकास, उत्पादन और बिक्री को एकीकृत करती है। वर्तमान में इसमें…
रुईयांग फार्मास्युटिकल कंपनी लिमिटेड एक व्यापक आधुनिक फार्मास्युटिकल कंपनी है जो अनुसंधान एवं विकास, उत्पादन और बिक्री को एकीकृत करती है। वर्तमान में इसमें 5,000 से अधिक कर्मचारी हैं और यह 1.2 मिलियन वर्ग मीटर के क्षेत्र को कवर करता है। यह एक राष्ट्रीय उच्च तकनीक उद्यम, बायोफार्मास्युटिकल औद्योगीकरण के लिए एक राष्ट्रीय रीढ़ उद्यम और एक राष्ट्रीय तकनीकी नवाचार प्रदर्शन उद्यम है। कंपनी का मुख्य व्यवसाय राजस्व कई वर्षों से शीर्ष 100 राष्ट्रीय दवा उद्योग उद्यमों में से शीर्ष 50 में रहा है।
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Shandong, China
- Website
- https://www.reyoung.cn
- Categories
- फार्मास्युटिकल विनिर्माण, पूरक और कल्याण
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
- 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. effective since 2025-02-22. EudraGMDP, EU register of GMP certificates (EMA)
- product-authorised-for-sale (record type: product-authorised-for-sale; this record does not by itself establish manufacturing) [official record; status green] A national regulator lists this company as the MAKER of products it has authorised for sale in that country. It is an export footprint you can check, not a quality rating: the register says the goods were allowed in, not that they are good. checked 2026-10-06. NAFDAC Greenbook, Nigeria - register of authorised products (manufacturer named on the authorisation)
- 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. Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
Relationships
1 relationship(s) on file. Each line names the other party, the relationship as its source records it, and the source. A record of a relationship is not a finding about control beyond what it literally says.
Candidates, not confirmed
- Zibo: Manufactures at the site. EudraGMDP, EU register of GMP certificates (EMA)
Import rules for these goods
Product-specific import rules not established for the catalog categories फार्मास्युटिकल विनिर्माण, पूरक और कल्याण: 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.