crf 00 29 01 00 42 40 forms may be

							                                         00:29:01 / 00:42:40




forms may be in either a paper or electronic format. The
sponsor designs the forms to capture the data required by
the protocol. The investigator or designate is to ensure
that source data is transcribed accurately and completely
from source documents to the paper CRF or the electronic
CRF. The sponsor or CRO will inform the investigator or        [00:26:24] Investigator's Responsibilities - Medical Records
designate of the required timelines for form completion.
                                                               [00:27:24] Sponsor-provided Progress Notes
Typically, sponsors expect case
                                                               [00:28:09] Access to Medical Records
                                                               [00:28:39] Case Report Form (CRF)
                                                               [00:29:30] Data Correction - Proper Procedures for CRFs/Source Documents
                                                               [00:30:37] Avoid Signature Irregularities