(a) The director or supervisor of approved tissue processing programs shall keep records of all tissues processed.
(b) Records may be designated by number (instead of by name of donor) to conform with individual specimens or lots of tissue.
(c) Records shall contain the following data:
(1) Name and address of institution from which material was obtained, also name of physician responsible for procurement.
(2) Date and hour of death of donor.
(3) Cause of death and age of donor and, when available, pathologic results including autopsy reports.
(4) Date and hour of obtaining tissue. If more than four hours post mortem, state whether refrigeration was used and, if so, give length of time and temperature.
(5) Date and method of processing tissue, if applicable.
(6) Date final storage begins.
(7) Date and place of use.
(8) Results of tests for contamination and other examinations.
(9) Pertinent laboratory data, including serologic tests for syphilis, from donor. Prospective donors with histories of hepatitis shall not be accepted.
(10) Information relating to consent or authorization.
(d) Unless otherwise required by other provisions of law, all records and information shall be retained for not less than two (2) years.