U.S. DOT's infectious substance transport rule includes new
training requirements for generators as well as tranporters.
On August 14, 2002, the U.S. Department of Transportation (DOT) issued revised
requirements for transporting infectious substances (Federal Register,
Vol. 67, No. 157, pp. 53118-53144). Infectious substances include etiologic
agents, regulated medical wastes, diagnostic specimens, and certain
biological products. These revisions have been made to conform to World
Health Organization criteria and to be consistent with the United Nations
Recommendations on the Transport of Dangerous Goods. The effective
compliance date for this
final rule is February 14, 2003.
"These rules have been proposed for over a year and a half now and are no
surprise to the medical waste industry," says Nelson "Sig" Slavik, Ph.D., of
Environmental Health Management Systems, Inc., Niles, MI. Slavik testified
before DOT on behalf of the American Hospital Association in 1993 and 1995
during the initial development of the rules. The medical waste industry and
applicable federal agencies – including the Centers for Disease Control and
Prevention, the Occupational Safety and Health Administration, and the
Environmental Protection Agency – have worked closely with the DOT to ensure
workable regulations.
Slavik notes, however, that what may come as a surprise is the
responsibility the medical facility has under DOT regulations. Of critical
concern is the training mandated for healthcare staff involved in the
labeling, containment, and manifesting of shipments of infectious substances
including regulated medical wastes and diagnostics specimens. Personnel in
most healthcare facilities are unaware of DOT training requirements for
off-site medical waste shipments, and now these requirements extend to
diagnostic specimens. The rules also apply to medical facilities actively
involved in research, shipping cultures and stocks of etiologic agents or
genetically modified organisms.
Employee training has been an ongoing DOT requirement for transporters of
any hazardous materials, including infectious substances. These training
requirements now extend beyond the transporter to the facility offering the
materials for shipment. The extent of the training depends on the activities
in which the medical facility engages when preparing the materials for
transport. Specific rules for training are found in 49 Federal Code of
Regulations Part 172.704. The healthcare facility should work closely with
its transporter to ensure that both the transporter and the hospital comply
with training requirements and other DOT requirements for packaging,
labeling, manifesting, and emergency response.
The final rule also includes new requirements for shipping diagnostic
specimens. Shipping requirements are minimal for those diagnostic specimens
containing Risk Group 2 or Risk Group 3 materials (as defined in the final
rule). All diagnostic specimens in these categories must be contained in
packaging meeting minimum performance criteria and must be marked
"Diagnostic Specimens." Diagnostic specimens in Risk Group 1 are not
regulated. Any specimen containing Risk Group 4 materials, however, is under
the full restrictions of Division 6.2, "Infectious Substances."
Healthcare facilities must familiarize staff with the requirements set
forth in the final rule. Ensure that your transporter knows the rules and
can provide you with the training required for your employees as well as the
packing and labeling materials required for your shipment.
This information was obtained from
Premier, Inc.'s Safety Share website
TRAINING LINKS:
US DOT - Office of
Hazardous Material Safety homepage
US DOT - Office of Hazardous Material Safety : Hazmat Regulations and Intrepretations
US DOT - Office of Hazardous Material Safety :
Hazmat Training Requirements
US DOT - Federal
Motor Carrier Administration homepage
US DOT - Federal Motor Carrier Administration :
Security Information