Celon Pharma
Obat generik, terapi pernafasan dan produk farmasi.
Celon Pharma memproduksi obat-obatan generik, terapi pernapasan, dan produk farmasi dari operasinya di Lomianki. Perusahaan ini memasok saluran farmasi, pembeli rumah sakit, distributor layanan kesehatan, atau pelanggan ekspor di seluruh pasar utama yang terdaftar.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Lomianki, Poland
- Founded
- 2002
- Website
- celonpharma.com
- Categories
- Perlengkapan Medis & Kesehatan, Suplemen & Kesehatan
- Markets
- Polandia, Jerman, Ceko, Hungaria
What is established and what is not
No facet of this company has been investigated yet. The facts below are collected records, not an assessment: nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Verified facts
- domain-registered (green), checked 2026-08-05 Domain registry record
- debarment-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- sanctions-clear (green), checked 2026-08-05 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- lei-active (green), checked 2026-08-05 GLEIF
- corporate-mail-on-domain (green), checked 2026-08-05 Mail server of the company domain
- operating-permit (green), checked 2026-08-19 EudraGMDP manufacturing authorisation register (EMA)
- registered-manufacturer (green), checked 2026-08-18 Chemistry, Food and Drugs Division, Ministry of Health of Trinidad and Tobago, register of drugs (Food and Drugs Act Chap. 30:01)
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Medical devices sold in the EU must carry CE marking under the Medical Device Regulation (EU) 2017/745, with a conformity assessment matched to the device risk class. European Commission (MDR)
- For the US market, the maker must have an FDA device establishment registration and product listing; most instruments also need 510(k) premarket clearance. US FDA (devices)