The Neo-ACT trial monitoring units

The Neo-ACT trial is conducted according to Good Clinical Practice requirements and monitored by Academic Research Organisations (AROs) alternatively Clinical Research Organisations (CROs) in each participating country.

Good Clinical Practice (GCP) is the international ethical, scientific, and practical standard to which all clinical research is conducted. It is important that everyone involved in research is trained or appropriately experienced to perform the specific tasks they are being asked to undertake.

Sweden:

CTO, Centrum för Kliniska Cancerstudier, Tema Cancer
Elite Carolina Tower, plan 3
Eugeniavägen 6
Karolinska Universitetssjukhuset
171 76 Stockholm
Sweden
 

Monitors:

Yvonne Larsén yvonne.larsen@regionstockholm.se

Natalia Pohl natalia.pohl@regionstockholm.se
 

Data manager:

Mats Hellström mats.hellstrom@regionstockholm.se

 

For Investigator Site File (SE: Prövarpärm) templates please refer to tab “Investigator Site File”.

 

Finland:

(TBC)