Pharmascience
Formulations pharmaceutiques, médicaments génériques et produits de santé.
Pharmascience fabrique des formulations pharmaceutiques, des médicaments génériques et des produits de santé à partir de ses opérations de Montréal. La société approvisionne les réseaux de pharmacies, les acheteurs d'hôpitaux, les distributeurs de soins de santé ou les clients exportateurs sur ses principaux marchés cotés.
- Type
- brand seeking distribution
- Location
- Montreal, Canada
- Founded
- 1983
- Website
- pharmascience.com
- Categories
- Fournitures médicales et de santé, Compléments et bien-être
- Markets
- Canada, États-Unis, Royaume-Uni, Australie
Verified facts
- domain-registered (green), checked 2026-08-09 Domain registry record
- debarment-clear (green), checked 2026-08-09 OpenSanctions
- sanctions-clear (green), checked 2026-08-09 OpenSanctions
- web-presence-since (green), checked 2026-08-09 Internet Archive (Wayback)
- corporate-mail-on-domain (green), checked 2026-08-09 Mail server of the company domain
- product-authorised-for-sale (green), checked 2026-08-21 Gobiernu di Korsou, Lijst maximumprijzen geneesmiddelen (bijlage bij de Regeling maximumprijzen geneesmiddelen)
- facility-registered (green), checked 2026-08-23 NPRI, National Pollutant Release Inventory (Environment and Climate Change Canada)
- registry-id-verified (green), checked 2026-06-04 Canada's Business Registries (federal + provincial, one search)
- lei-lapsed (amber), checked 2026-08-23 GLEIF global LEI register (golden copy)
- 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
- Good Manufacturing Practice
- ISO 9001, Quality Management IAF CertSearch
Import rules for these goods
- Food supplements sold in the EU follow Directive 2002/46/EC: most member states require a notification to the national authority before the first sale. European Commission (supplements)
- 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)