Cotupha
Tunesisch farmaceutisch bedrijf dat cosmeceuticals en dermatologische preparaten produceert.
Cotupha produceert farmaceutische en cosmeceutische producten, waaronder dermatologische preparaten en huidverzorgingsformuleringen voor de Tunesische gezondheidszorg- en apotheekmarkt. Het bedrijf opereert onder GMP-normen vanuit zijn productiefaciliteit in Tunis.
- Type
- manufacturer (our classification of the record, not a statement by the company)
- Role
- Manufacturer
- Location
- Tunis, Tunisia
- Founded
- 1993
- Website
- https://www.cotupha.com
- Categories
- Huidverzorging en cosmetica, Medische en gezondheidszorgbenodigdheden
- Markets
- Tunesië
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 2026-08-08 Domain registry record
- sanctions-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- debarment-clear (green), checked 2026-08-08 - screened by name only: no legal entity is established for this record, so this is not a clearance OpenSanctions
- corporate-mail-on-domain (green), checked 2026-08-08 Mail server of the company domain
Claimed certifications, not confirmed by us
- Good Manufacturing Practice
Import rules for these goods
- Cosmetic products must be notified in the EU Cosmetic Products Notification Portal (CPNP) before being placed on the EU market. European Commission (CPNP)
- For the US market, MoCRA requires cosmetic facility registration and product listing with the FDA. US FDA (MoCRA)
- 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)