Sut gall y tîm Systemau Gwybodaeth CHIGC gefnogi eich astudiaeth?
Mae tîm IS NWORTH yn gweithio'n agos gyda thimau astudio i gynnig atebion ar gyfer dal data electronig yn y profion ac yn sicrhau cywirdeb data o'r pwynt mynediad, to management, through to data lock. We design trial software, databases, and systems (e.g. Electronic Data Capture system, Randomisation system), ensuring these are designed in a manner to meet the needs of all end users, including study staff, analysts and participants. We validate every system to provide study teams with a high degree of assurance that the system will consistently meet its predetermined specifications and quality, and will be fit for purpose in line with Good Clinical Practice (GCP). Our validation process is ongoing, meaning that we continuously review to make sure the system remains in a validated state throughout its lifetime.
Bydd y tîm TG yn eich cefnogi gyda:
- Ffurflen Adroddiad Achos electronig (eCRF) / dylunio CRF
- Dylunio cronfeydd data
- Mewnbynnu data
- Dilysu, cymhwyso a phrofi meddalwedd
- Cyfrinachedd a diogelwch data
- Cefnogaeth defnyddwyr a datrys ymholiadau
- Rhewi a chloi data
Mae gan ein tîm NWORTH IS wybodaeth drylwyr am Arfer Clinigol Da (GCP), fframwaith polisi'r DU ar gyfer treialon clinigol, a Rheoliadau Treialon Clinigol, gan sicrhau bod data'n cael ei drin yn briodol yn unol â Deddf Diogelu Data 2018, y Rheoliadau Diogelu Data Cyffredinol (GDPR), GCP a deddfwriaeth berthnasol arall.