Glossary

Resources - Glossary - Illustration

A

C

Clinical Research Coordinator (CRC)

Clinical Study Design

Clinical Study Design Types

Concomitant Treatment or Medication

D

E

Eligibility Criteria

Exclusion Criteria

F

H

I

Inclusion Criteria

Informed Consent

Institutional Review Board (IRB)

Investigational Product (IP)

O

Open Label Extension Study

P

Patient Reported Outcome (PRO)

Phases of a Trial

Principal Investigator (PI)

R

S

Screening Period

Screening Visit

Serious Adverse Event

Standard of Care

Study Withdrawal

T

Treatment Group or Treatment Arm

Treatment or Drug

W

Wash-out Period