ICF
Investigational Product
Temperature Excursions
AE, SAE, TEAE, Oh My!
I'm a Lead!
100

Document used to inform patients about their rights, the risks, & benefits of participating in a research study.

what is: informed consent form

100

Prior to handling any investigational product (receiving/dispensing/returning), one must have _____ in his/her hands

what is: red drug folder

100

Oh no your drug just experienced a temperature excursion! The first thing you should do is 

What is: contact your manager

100

The amount of time to report if your patient experience a Serious Adverse Event

what is: 24 hours

100

The first place to become acquainted with a high-level overview of a new study.

what is informed consent form

200

The acronym is TASC, the meaning behind each letter is

What is: Time Ask Sign Copy

200

Once IP has arrived and has been properly checked in and logged on the drug log, where must the paperwork & drug log be uploaded

Where is: Basecamp Supplies Receipt

200

When IP has been exposed to unfavorable conditions, the IP must be 

what is: quarantined

200

Your patient has experienced an SAE, the first thing you should do is populate the _______ to do list in ______

What is:  "I have an SAE, now what?! & Basecamp

200

You should have your first _______ scheduled within one ______ of your site initiation visit

what is: screen & week

300

The location where ICFs can be found and printed on the day of the visit

What is: Drive

300

Prior to administering IP to a patient, the dispenser should always check these two things first

what are: temperature in range & kit unexpired 

300

Prior to dispensing IP that has experienced an excursion, study personnel should obtain what first

what is: confirmation in WRITING

300

An adverse event is any _______ event associated with the use of an investigational product, regardless of whether or not it is related to the investigational product

What is: untoward

300

If the enrollment goal on a study is 10 and you currently have 4 patients enrolled, you should have a minimum of _____ patients scheduled

What is: 6

400

The document that outlines how informed consents are obtained is

What is: SOP (standard operating procedure)

400

Prior to handling IP and/or writing on a drug log, staff should be

what is: delegated

400

IP that has been quarantined should be placed in a separate bag with all of the paperwork surrounding the excursion and it should be stored in 

What is: the same storage conditions required when in range (fridge/freezer/ambient - locked/limited access)

400

A delegated PI/SI must be the one to assess the _____ & _____ to investigational product for all adverse events

what is: severity & relatedness

400

When populating recruitment lists into RealTime call rosters for a new study, what patients should be prioritized?

What is: Past Study Patients (Low hanging fruit)

500

The subject must sign the informed consent prior to 

What is: initiating any study related procedures

500

The IP receipt stamp includes steps that must be followed when IP is received at the site; those steps include

What is: stop temp tale, fax/return completed form, complete drug log, log in IVRS & print confirmation

500

The temperature for IP is documented in _____ & the ______ & _______ & ______ should be documented saily

What is: Drive, Minimum, Maximum, & Current temperatures

500

DocTrials documents PI oversight of Adverse Events & Serious Adverse Events by _______

What is: having the PI sign off on ALL subject AE/SAE at the time of the patient's exit visit

500

Recruiting subjects can be challenging; the primary ways to identify patients that we have found the most success are: _____, _____, _____, & ______

what are: RealTime (past study patients), doctor referrals, chart review, & community outreach 

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