APL
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.
APL är en av Europas största tillverkare av extemporeläkemedel och lagerberedningar samt en ledande kontraktstillverkare inom Life Science-i
APL est une organisation scandinave de développement et de fabrication sous contrat (CDMO) leader dans le secteur des sciences de la vie, dédiée au développement, à la fabrication et à l'analyse de produits pharmaceutiques.…
- Type
- Not established by any record (our catalog import lists it as manufacturer; that is not evidence of the role)
- Role
- Role not established by any record
- Location
- Sweden
- Website
- http://apl.se
- Categories
- Production pharmaceutique
Listed in a source registry
What is established and what is not
No researcher review has been written for this company yet. No official record is 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. Nothing here confirms manufacturing, ownership or trading status beyond what each record literally says.
Facts on file, each with its evidence type
- Business email on the company's own domain (record type: corporate-mail-on-domain) [our own observation, not an official record; status green] Shows the domain runs its own email rather than a free mailbox. It describes the domain, not who owns it. checked 2026-08-04. Mail server of the company domain
- Legal entity ID lapsed (record type: lei-lapsed-by-name) [our own observation, not an official record; status amber] A search of the GLEIF register by company name found an identifier under this name that was not renewed. The match is by name only, so it may belong to another legal entity. checked 2026-08-04. GLEIF
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.