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Hi, Still quite an OpenC novice, saw this online....
For recording of adverse events and concomitant medications it is advised not to design the OpenClinica Events as repeating; the event repeats (or Event occurrences) will get a number and it is not clear for the data entry person which AE/con-med belongs to which number. Instead, it is advised to implement repeating item group(s) in the AE/con-med Crf to be able to record multiple AEs/con-meds for one subject and add this Crf to a non-repeating event
I do not have the OC knowledge to critique the veracity of the above, in fact I must admit I do not 100% understand it - please may anyone explain what it means & confirm this is indeed the case for best-practices?
Many thanks in advance for any assistance.