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cIRB
Reg Docs
Reliance Policy
Abbreviations
CTAs
100

OHRP

What is Office of Human Research Protections

100
You must contact this department when you have a new protocol that involves a study drug.
What is the Investigational Pharmacy?
100
The buck stops here
Who is the principal investigator?
100

cIRB

What is the Central Institutional Review Board?

100

It is ACRP's color palette

What is blue, green and yellow

200
CRF
What is Case Report Form?
200
The phase of clinical research involves a small number of subjects and is the first time a drug is used in humans.
What is a Phase One Clinical Trial?
200
a process in which researcher (or appropriately trained designee) discloses all relevant information about a study, a potential subject has opportunity to ask questions, and researcher answers questions.
What is the informed consent process?
200

CTA

What is Clinical Trial Agreement?

200

21 members and growing

What is the St Louis ACRP Chapter?

300
IND
What is Investigational New Drug?
300
This report describes respect, beneficence and justice as key components of clinical research on humans subjects.
What is the Belmont Report?
300

Relying Institution

What is another name for a site?

300
Serious, Unexpected, Related to the study and Occurring on a trial that is open at a site subject to CPHS review.
What is a Serious Adverse Event as defined by the CPHS?
300

It's the date the St Louis Chapter was (re)launched

July 31, 2024

400
HIPAA
What is the Health Insurance Portability and Accountability Act?
400

Graphic display of schedule of activities/visits in a research protocol.

What is the schema/schedule of events?

400
This process must occur before any study related activities occur with a potential participant (unless waived or altered by the IRB).
What is the informed consent discussion and signing of the informed consent document?
400

Publication rights

What is an issue in negotiating a clinical trial agreement?

400

It is the closest chapter to Saint Louis at 247 miles (397 km) driving distance

What is the Kansas City chapter

500
DSMB
What is the Data and Safety Monitoring Board?
500
An original record of an event
What is source documentation?
500
This provides public assurance that the rights, safety and well-being of human subjects involved in research are protected.
What is GCP compliance?
500

You must have IRB approval before you do this.

What is recruit subjects for a clinical trial?

500

It's a community of professionals in the clinical research space

What is an ACRP Chapter?