Klinik Araştırmalarda Yaygın Olarak Kullanılan Kısaltmaların Kısa Listesi

Son güncelleme: Ağustos 17, 2026

 

Klinik Araştırmalarda Yaygın Olarak Kullanılan Kısaltmaların Kısa Listesi

700U Statement of Economic Interest

ACRP Association of Clinical Research Professionals

AE Adverse Event

ADR Adverse Drug Reaction

AMA American Medical Association

BID Twice Daily

BIND BiologicalIND

CAP Collegeof American Pathologists

CBCTN Topluluk Tabanlı Klinik Araştırmalar Ağı

CBER Centerfor Biologics Evaluation and Research (FDA)

CCRA Certified Clinical Research Associate (ACRP)

CCRC Certified Clinical Research Coordinator (ACRP)

CCRC CTSC ClinicalResearchCenter

CCRP Certified Clinical Research Professional (SoCRA)

CDA Confidential Disclosure Agreement

CDC Centerfor Disease Control

CDER Centerfor Drug Evaluation and Research (FDA)

CDRH Centerfor Devices and Radiological Health (FDA)

CF Consent Form

CFR Code of Federal Regulations

CLIA Clinical Laboratory Improvement Amendments

CME Continuing Medical Education

CP Compliance Program (FDA)

COI Conflict of Interest

CRA Clinical Research Associate CTSC Clinical Research Training Program

CRC Clinical Research Coordinator

CRF Case Report Form

CRO Clinical Research Organization

CT Clinical Trial

CTA Clinical Trial Agreement

CS Clinically Significant

CSA Clinical Service Agreement

CTSC Clinical and TranslationalScienceCenter

CV Curriculum Vitae

DCF Data Correction Form / Data Clarification Form

DEA Drug Enforcement Agency (FDA'nın kanun uygulama bölümü)

DHHS Department of Health & Human Services

DOS Description of Study

EAB Ethical Advisory Board (IRB'ye benzer, diğer uluslar tarafından kullanılan)

EDC Electronic Data Capture

FDA Food and Drug Administration

FDA-482 Denetim Bildirimi

FDA-483 Notice of Adverse Findings in an Inspection

FDA-1572 FDA Form for New Drug Application

FDA-1572 FDA Araştırmacı Beyanı Formu

FDA-SRS FDA'nın Spontan Raporlama Sistemi

FDCA Food, İlaç, ve Kozmetik Yasası

FOIA Freedom of Information Act

FTC Federal Ticaret Komisyonu

GCP Good Clinical Practice

GDA Global Disclosure Agreement

GLP Good Laboratory Practice CTSC Clinical Research Training Program

 

GMP Good Manufacturing Practice

HIPAA Health Insurance Portability and Accountability Act

HHS Health and Human Services (Bölümü)

HMO Health Maintenance Organization

IACUC Institutional Animal Care and Use Committee (IRB for animal use)

IB Investigator’s Brochure

 

ICF Bilgilendirilmiş Onam Formu

ICH Uluslararası Uyumlaştırma Konferansı

IDB Araştırma İlaç Broşürü

IDE Araştırma Cihazı Muafiyeti

IDS Araştırma İlaç Hizmeti (eczane)

INAD Araştırmaya Yönelik Yeni Hayvan İlacı (FDA)

INDInvestigational New Drug

IRB Kurumsal İnceleme Kurulu

JCAHO Sağlık Kuruluşlarının Akreditasyon Ortak Komisyonu

LOA Anlaşma Mektubu

MDR Medical Device Reporting

MOU Memoranda of Understanding

MRA Tıbbi Araştırma Görevlisi

NAI No Action Indication (most favorable post-FDA inspection classification)

NCI National Cancer Institute

NCS Klinik Açıdan Anlamlı Değil

NDA Yeni İlaç Başvurusu

NHLBI National Heart, Akciğer, and Blood Institute

NIAID National Institute of Allergy and Infectious Diseases CTSC Clinical Research Training Program

 

NIH Ulusal Sağlık Enstitüleri

NIMH Ulusal Ruh Sağlığı Enstitüsü

NKA Bilinen Alerjisi Yok

OAI Official Action Indicated (serious post-FDA inspection classification)

OHRP Office for Human Research Protection

OSHA Occupational Safety and Health Administration

OTC Over-the-counter (non-prescription drugs)

OVCR Office of the Vice Chancellor for Research

PCCPoisonControlCenter

PD Pharmacodynamics

PDQ Physician’s Data Query (NCI sponsored cancer trial registry)

PDR Physician’s Desk Reference

PE Physical Examination

PHI Korumalı Sağlık Bilgileri

PI Paket Eklemesi

PI Principal Investigator

PK Farmakokinetiği

PLA Product License Application (when seeking commercialization of a biologic)

PMA Pazar Öncesi Onayı (bir cihazın ticarileştirilmesi istendiğinde)

POBy Mouth

PPE Personal Protective Equipment

PPI Patient Package Inserts

PPO Preferred Provider Organization

Gerektiğinde PRN

QA Quality Assurance

QC Quality Control

QD Every day CTSC Clinical Research Training Program

 

QID Günde Dört Defa

QOL Quality of Life

R&D Research and Development

RDE Uzaktan Veri Girişi

RL Regulatory Letter (post-FDA audit letter)

Rx. Prescription

SAE Serious Adverse Event

SC Çalışma Koordinatörü

SD Source Document

SMO Site Management Organization

SoCRA Klinik Araştırma Görevlileri Derneği

SOMSchoolof Medicine

SOP Standart İşletim Prosedürü

SRA Personeli Araştırma Görevlisi

Günde Üç Kez TID

UNK Unknown

USPU.S.Pharmacopeia

VAUnited StatesDepartment of Veterans Affairs

VAI Voluntary Action Indicated (post-FDA audit inspection classification)

VS Yaşamsal Belirtiler

DSÖ Dünya Sağlık Örgütü

WL Warning Letter