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