novelty pharma gdd sa
Novelty Pharma - Innovazione farmaceutica bruisend
Bruisende farmaceutische innovatie Meer informatie over het bedrijf Al meer dan 25 jaar ontwikkelen wij farmaceutische producten en voedingssupplementen. Wij zijn een kenniscentrum in de zorgsector, gespecialiseerd in farmacie, voeding en cosmetica, met een missie: anticiperen op de toekomst. Dankzij onze voortdurende aandacht voor markttrends stimuleren we innovatie en creëren we geavanceerde producten
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Cadempino, Switzerland
- Website
- https://www.noveltypharma.com
- Categories
- Farmaceutische productie, Medische en gezondheidszorgbenodigdheden, Supplementen & Welzijn
Listed in a source registry
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 2026-08-02 Domain registry record
- web-presence-since (green), checked 2026-08-03 Internet Archive (Wayback)
- sanctions-clear (green), checked 2026-07-21 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
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)
- 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)