Phytopharm Kleka S.A.
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.
Start - PhytoPharm
Phytopharm Kleka S.A. , авторитетный поставщик для фармацевтической промышленности, специализирующийся на производстве высококачественных активных фармацевтических ингредиентов (API). Компания широко известна…
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Poland
- Website
- http://phytopharm.pl
- Categories
- Фармацевтическое производство
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. 7 official records from 6 official sources are on file. 1 other entry is not an official record: our own technical checks and searches, open directory listings, our inferences or the company's own statements. 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
- Website domain registered (record type: domain-registered) [our own observation, not an official record; status green] Shows how long this web address has been registered. That is the age of the domain, not of the company: a domain can change owners. checked 2026-08-11. Domain registry record
- 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 2025-09-30. EudraGMDP, EU register of GMP certificates (EMA)
- Street address on file in the state register (record type: registered-address) [official record; status green] Registered address: KLĘKA 1, 63-040 KLĘKA. The address the company itself gave the register, so post and inspectors reach it there. checked 2026-10-03. Ministry of Finance VAT white list (Poland)
- Medicines manufacturing or import authorisation (MIA) (record type: medicines-mia-holder) [official record; status green] A medicines regulator authorises this company to manufacture and/or import medicinal products at the named site. The register lists the authorisation itself, not which products it covers, and it is not a record of trading. checked 2026-08-15. EudraGMDP manufacturing and importation authorisation register (EMA)
- Line of business as recorded in the state register: PRODUKCJA LEKÓW I POZOSTAŁYCH WYROBÓW FARMACEUTYCZNYCH (record type: registry-activity) [official record; status green] Line of business as recorded in the state register: PRODUKCJA LEKÓW I POZOSTAŁYCH WYROBÓW FARMACEUTYCZNYCH. Shows what the state itself says the company does, which you can compare with what it promises you. checked 2026-10-03. REGON national business register (GUS, Poland)
- product-authorised-for-sale (record type: product-authorised-for-sale-holder; this record does not by itself establish manufacturing) [official record; status green] A national regulator lists this company as the holder of the registration of products it has authorised for sale in that country. The holder answers for the product on that market; the record does not say the holder makes it. checked 2026-10-03. Superintendencia de Regulacion Sanitaria de El Salvador, listado de productos farmaceuticos con registro sanitario vigente
- EU VAT number valid for cross-border trade (record type: vat-valid) [official record; status green] The number is registered and active: we asked the EU VIES service and it answered yes. An invalid VAT number is the first sign an invoice comes from the wrong company. checked 2026-08-01. VIES (European Commission)
- 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
Import rules for these goods
- Medicines imported into the EU must come from a site holding an EU GMP certificate, and the importer needs a manufacturing/import authorisation. European Medicines Agency (GMP)