Investigation site management
We help you in finding the right investigation sites with a competent and motivated personnel.
Site selection
We work closely with specialized study centers, hospitals and medical offices to select a site/sites with a patient population and recruitment potential that is optimal for your device. Our experts conduct site qualification visits to ensure suitability for your clinical investigation. We prepare budgets and negotiate contracts with the healthcare units.
Monitoring
We prepare a monitoring plan and monitor the investigation.
Site management
We make sure the study personnel are trained in the use of your device and the study protocol. Our experts keep regular contact with the sites to ensure data quality.
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Latest news
Meet us at RAPS in Berlin on May 6-8!
Visit our booth TB1 in the RAPS exhibition and hear about regulatory affairs services for and MD/IVD manufacturers.Meet us in Tomar, Portugal
Labquality will attend SPML's (Sociedade Portuguesa de Medicina Laboratorial) 16th scientific meeting in Tomar, Portugal, from 12 to 13 April 2024.Meet us at ECCMID in Barcelona
Visit our booth E5 in the ECCMID exhibition and hear about EQA services for microbiology, as well as CRO services for pharmaceuticals and MD/IVD manufacturers.Why Modeling Data Flows Is Needed in Clinical Investigations
data management manager explains how data flow modeling will help keep clinical investigation stakeholders informedEQA Coordinator Anna-Riitta Vanhanen Retires After 34 Years of Service
EQA Coordinator Anna-Riitta Vanhanen is retiring in the autumn of 2024 after working at Labquality since 1990. Biochemist Hanna Heikkilä will take over Anna-Riitta's EQA rounds.Subscribe to our newsletter
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