Pharmascience
फार्मास्युटिकल फॉर्मूलेशन, जेनेरिक दवाएं और स्वास्थ्य देखभाल उत्पाद।
फार्मासाइंस अपने मॉन्ट्रियल परिचालन से फार्मास्युटिकल फॉर्मूलेशन, जेनेरिक दवाएं और हेल्थकेयर उत्पाद बनाती है। कंपनी अपने सूचीबद्ध प्राथमिक बाजारों में फार्मेसी चैनल, अस्पताल खरीदारों, स्वास्थ्य सेवा वितरकों या निर्यात ग्राहकों को आपूर्ति करती है।
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Montreal, Canada
- Founded
- 1983
- Website
- pharmascience.com
- Categories
- चिकित्सा एवं स्वास्थ्य देखभाल आपूर्तियाँ, पूरक और कल्याण
- Markets
- कनाडा, संयुक्त राज्य, यूनाइटेड किंगडम, ऑस्ट्रेलिया
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 2026-08-09 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)
- registry-id-verified (green), effective since 2026-06-04 Canada's Business Registries (federal + provincial, one search)
- lei-lapsed (amber), checked 2026-09-07 GLEIF global LEI register (golden copy)
- facility-registered (green), checked 2026-08-23 NPRI, National Pollutant Release Inventory (Environment and Climate Change Canada)
- 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
- 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)