Adifarm EAD
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.
국가 의약품 기관으로부터 라이센스를 받은 불가리아 제약 제조업체입니다.
불가리아 의약품청은 2026년 7월 6일 발행된 승인 BG/MIA-0582에 따라 제조 승인 등록부에 이 회사를 등록했습니다. 승인에는 비멸균 의약품, 2차 포장이 포함됩니다. 국가 등록부에 등록된 이름: Адифарм ЕАД.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer (official record)
- Location
- Sofia, Bulgaria
- Categories
- 의약품 제조
Listed in a source registry
Bulgarian Drug Agency (ИАЛ), registers of manufacturers, importers and traders
What is established and what is not
No researcher review has been written for this company yet. 2 official records from 1 official source are on file. 2 other entries are not official records: 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
- Registered as a manufacturer (record type: registered-manufacturer) [official record; status green] Its own declared activity in the register covers making these goods. checked 2026-08-20. Bulgarian Drug Agency, register of manufacturing and import authorisations (art. 19, Medicinal Products Act)
- Operating permit for the production site (record type: operating-permit) [official record; status green] Shows an authority issued a permit for an installation at this site for the activity named in the record. A permit is not an inspection report and not an observation that production is running today. checked 2026-08-20. Bulgarian Drug Agency, register of manufacturing and import authorisations (art. 19, Medicinal Products Act)
- No match found on the sanctions lists we checked (record type: sanctions-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public sanctions datasets and found no matching candidate. A name search is not full compliance screening. Screened by name only: no legal entity is established for this record, so this is not a clearance. checked 2026-08-31. OpenSanctions
- No match found in the debarment registers we checked (record type: debarment-clear) [our own observation, not an official record; name search, no matching candidate] We searched the public debarment datasets and found no matching candidate. Absence from these lists is a search result, not a certificate. Screened by name only: no legal entity is established for this record, so this is not a clearance. checked 2026-08-31. OpenSanctions
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
- Bul. „Simeonovsko Shose” №130, Gr. Sofiya (бул. „Симеоновско шосе” №130, гр. София): Holds the site's permit, registry number manufacturing authorisation (разрешение за производство). Bulgarian Drug Agency, register of manufacturing and import authorisations (art. 19, Medicinal Products Act)
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)
Check independently
Before a first order, ask for the legal entity's registration number and country, then check it in the official register.