Ametlik kokkuvõte · English
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To appoint external Clinical Research Associates/study monitors that will deliver the monitoring element of University’s sponsored regulated and post-market medical device clinical trials in line with the agreed monitoring strategy/plan, provide site management, and provide in-country knowledge and support for this and regulatory submissions and resubmissions.
Allikas ja usaldusväärsus
Allikas: ametlik TEDi teade 269627-2026, viimati kontrollitud 21. aug 2026 22:05. Määravaks jääb algne väljaanne.
Andmed on lihtsamaks lugemiseks ümber struktureeritud. Alati on ülimuslikud ametlik teade ja hankedokumendid.