LOL
SIV
Site Initiation Visit
UAT
Unit Acceptance Testing
PI
Principal Investigator
CMP
Change Management Plan
DCR
Data Change Request
ICF
Informed Consent Form
GCP
Good Clinical Practice
QC
Quality Control
LPLV
Last Patient Last Visit
MDM
Mobile Device Management
CRO
Contract Research Organization
QMS
Quality Management System
GDP
Good Documentation Practice
KOL
Key Opinion Leader
RMA
Return Merchandise Authorization
SIM
Subscriber Identity Module
SOP
Standard Operating Procedure
PHI
Protected Health Information
IEC
Independent Ethics Committee
JAMA
Journal of the American Medical Association
CDA
Confidentiality Disclosure Agreement
CRF
Case Report Form
SMEs
Subject Matter Experts
IRBs
Institutional Review Boards
SLA
Service Level Agreement