Armenia
Regulatory authority and central ethics committee review together, 60 working days. No local ethics committees. All submissions in electronic format. Documents in Armenian and Russian. Site negotiations four weeks. A fully equipped bioequivalence site is available to sponsors as part of a Paspigioni-run study.
Country engagements
7 country engagements since 2015.
Review timelines
Regulatory authority and central ethics committee together, 60 working days.
Observed review periods from our own submissions, not statutory best cases. Where a query round arises, add roughly a month.
What we offer there
- Our own CRAs, monitoring at site
- Our own regulatory specialists for authority and ethics submissions, in the local language
- Site identification, feasibility and qualification
- Site contracts and budget negotiation
- Import, export and clinical logistics