Worked on a Phase I Clinical Trial Conducted a study visit at HMRC Worked on a clinical trial for a medical device Never used OnCore Worked with Human Factors team Worked on a phase II clinical trial Completed GCP course Submitted an ethics modification on IRISS Consented patient over the phone Faxed a document Never summitted an SAE report to REB Attended a site initiation visit Has a Clinicaltrials .gov account Has an IRISS account Worked on a study from start to closure Offered regulatory advice & inspection support Created a study budget Submitted REB renewal Used Connect Care for pre screening Had a audit visit Used CSM legal Created an informed consent form Submitted a protocol deviation Submitted a study invoice for processing Worked on a Phase I Clinical Trial Conducted a study visit at HMRC Worked on a clinical trial for a medical device Never used OnCore Worked with Human Factors team Worked on a phase II clinical trial Completed GCP course Submitted an ethics modification on IRISS Consented patient over the phone Faxed a document Never summitted an SAE report to REB Attended a site initiation visit Has a Clinicaltrials .gov account Has an IRISS account Worked on a study from start to closure Offered regulatory advice & inspection support Created a study budget Submitted REB renewal Used Connect Care for pre screening Had a audit visit Used CSM legal Created an informed consent form Submitted a protocol deviation Submitted a study invoice for processing
(Print) Use this randomly generated list as your call list when playing the game. There is no need to say the BINGO column name. Place some kind of mark (like an X, a checkmark, a dot, tally mark, etc) on each cell as you announce it, to keep track. You can also cut out each item, place them in a bag and pull words from the bag.
Worked on a Phase I Clinical Trial
Conducted a study visit at HMRC
Worked on a clinical trial for a medical device
Never used OnCore
Worked with Human Factors team
Worked on a phase II clinical trial
Completed GCP course
Submitted an ethics modification on IRISS
Consented patient over the phone
Faxed a document
Never summitted an SAE report to REB
Attended a site initiation visit
Has
a Clinicaltrials .gov account
Has an IRISS account
Worked on a study from start to closure
Offered regulatory advice & inspection support
Created a study budget
Submitted REB renewal
Used Connect Care for pre screening
Had a audit visit
Used CSM legal
Created an informed consent form
Submitted a protocol deviation
Submitted a study invoice for processing