Conducted a study visit at HMRC Created a study budget Never summitted an SAE report to REB Worked on a Phase I Clinical Trial Consented patient over the phone Worked on a phase II clinical trial Worked on a clinical trial for a medical device Worked with Human Factors team Submitted REB renewal Created an informed consent form Had a audit visit Has an IRISS account Submitted a protocol deviation Attended a site initiation visit Submitted a study invoice for processing Worked on a study from start to closure Used CSM legal Submitted an ethics modification on IRISS Never used OnCore Used Connect Care for pre screening Faxed a document Completed GCP course Offered regulatory advice & inspection support Has a Clinicaltrials .gov account Conducted a study visit at HMRC Created a study budget Never summitted an SAE report to REB Worked on a Phase I Clinical Trial Consented patient over the phone Worked on a phase II clinical trial Worked on a clinical trial for a medical device Worked with Human Factors team Submitted REB renewal Created an informed consent form Had a audit visit Has an IRISS account Submitted a protocol deviation Attended a site initiation visit Submitted a study invoice for processing Worked on a study from start to closure Used CSM legal Submitted an ethics modification on IRISS Never used OnCore Used Connect Care for pre screening Faxed a document Completed GCP course Offered regulatory advice & inspection support Has a Clinicaltrials .gov account
(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.
Conducted a study visit at HMRC
Created a study budget
Never summitted an SAE report to REB
Worked on a Phase I Clinical Trial
Consented patient over the phone
Worked on a phase II clinical trial
Worked on a clinical trial for a medical device
Worked with Human Factors team
Submitted REB renewal
Created an informed consent form
Had a audit visit
Has an IRISS account
Submitted a protocol deviation
Attended a site initiation visit
Submitted a study invoice for processing
Worked on a study from start to closure
Used CSM legal
Submitted an ethics modification on IRISS
Never used OnCore
Used Connect Care for pre screening
Faxed a document
Completed GCP course
Offered regulatory advice & inspection support
Has
a Clinicaltrials .gov account