Professional Documents
Culture Documents
Electronic prescribing
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The Australian Government, in collaboration with states and territories, has accelerated the delivery
of electronic prescribing to help protect people most at-risk from COVID-19. Electronic prescribing,
where available in the community, will provide patients with a choice to receive either an electronic or
a paper prescription from their prescriber. Visit the Electronic Prescriptions
[https://www.digitalhealth.gov.au/get-started-with-digital-health/electronic-prescriptions] website
for more information.
An exemption [https://www.health.nsw.gov.au/pharmaceutical/Documents/exemption-
eprescriptions-sep20.pdf] from the NSW Poisons and Therapeutic Goods Regulation has been
granted to allow electronic prescriptions to be legally issued and dispensed in NSW.
On this page
1. Information for software vendors
2. Information for prescribers
3. Information for community pharmacists
NSW requirements
For an electronic prescription to be legally valid in NSW, all systems participating in the prescribing,
transmission and dispensing of the prescription must be listed on the ADHA Electronic Prescribing
Conformance Register [https://www.digitalhealth.gov.au/about-us/policies-privacy-and-
reporting/registers] with a Conformance ID. Such a prescription is then termed a 'Conformant
Electronic Prescription'.
PRES-13
Electronic prescriptions are accepted in all circumstances where systems are conformant (i.e. each
participating system has a Conformance ID) and the prescription contains all required details (see
PRES-17).
PRES-17
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For an electronic prescription to be legally valid for dispensing in NSW it must contain the details
listed below. This list incorporates prescription requirements under the Poisons and Therapeutic
Goods Regulation 2008. (Where possible, Reference IDs from the Conformance Profile are listed).
Notes
restricted medicines.
The NSW Authority number is issued by the NSW Ministry of Health and is alphanumeric in
format, and may be prefixed with a text string of letters/characters, including 'AU', 'CNS', 's28c',
'CL', 'RA', and 'PG(T)'. Examples are AU123456789, RA998.
a Type A drug of addiction (see clause 122 of the Poisons and Therapeutic Goods Regulation
2008), i.e. Schedule 8 psychostimulants and pharmacist-compounded Schedule 8 medicines
a Schedule 4 (S4) medicine listed in clause 37 of the Poisons and Therapeutic Goods
Regulation 2008 (e.g. clomiphene, isotretinoin) (or as specified in Note 5)
5. For S4 medicines listed in clause 37 of the Poisons and Therapeutic Goods Regulation 2008 (e.g.
clomiphene, isotretinoin) the prescription must include either:
the prescriber’s specialist qualification (abbreviation is acceptable and could be up to 12
alphabetical characters) AND the text “issued under clause 37 of the Poisons and
Therapeutic Goods Regulation 2008” or words to that effect, OR
the NSW Authority number (see Note 4).
Some requirements for paper prescriptions do not apply to Conformant Electronic Prescriptions.
Prescribers of Conformant Electronic Prescriptions do not need to comply with the following paper
prescription requirements:
Pharmacists dispensing Conformant Electronic Prescriptions are exempted from the following paper
prescription requirements:
endorse in ink:
the date of dispensing
the pharmacy address
the prescription reference number
the word 'CANCELLED' where no valid repeat supplies remain
PRES-23
Under the Poisons and Therapeutic Goods Regulation 2008, a person issuing a prescription for a
Schedule 4 medicine listed in Appendix D of the Poisons and Therapeutic Goods Regulation 2008
[https://www.health.nsw.gov.au/pharmaceutical/Pages/sch4d.aspx] (S4D) or a S8 medicine must
keep a record of it for a period of at least two (2) years.
Medical records otherwise must be kept as required under the Health Practitioner Regulation
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National Law. They should be retained in a retrievable format and readable state for their minimum
required retention period.
PRES-24
DISP-4
While there is no requirement for each dispenser to login for each dispense transaction, the
pharmacist authorising a dispense event must ensure their identity is recorded against each dispense
event, for example, by entering their initials before each dispense event.
DISP-33
The NSW Poisons and Therapeutic Goods Regulation 2008 has no mandatory requirement to record
receipt of supply in the dispensing system.
For opioid substitution therapy, the pharmacist may record that the dose has been received by the
patient.
DISP-34
All records must be retrievable in human readable format immediately by any pharmacist in charge at
any time at the premises where the prescription was dispensed and retained for two (2) years from
the date of dispensing.
DISP-36
All dispense records must be retrievable in human readable format immediately by any pharmacist in
charge at any time at the premises where the prescription was dispensed and retained for two (2)
years from the date of dispensing.
DISP-51
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Records (prescribing and dispensing) must be searchable, filterable and retrievable by categories
including by patient, by prescriber, by drug, by legal category (at least S8, S4B, S4D, and S4, and
optionally S3, S2, and unscheduled).
DISP-50
PRES-17 provides a list of prescription details required to be displayed to the dispensing pharmacist.
MI-10
Records must be immediately retrievable in human readable format at the premises and retained for
two (2) years.
MI-10A
Records (prescribing and dispensing) must be searchable, filterable and retrievable by categories
including by patient, by prescriber, by drug, by legal category (at least S8, S4B, S4D, and S4, and
optionally S3, S2, and unscheduled).
A separate approval from NSW Health is not required where a system conforms under the Electronic
Prescribing Conformance Assessment Scheme and has been listed on the Electronic Prescribing
Register of Conformance with a Conformance ID.
Prescribers must ensure that the electronic prescription created by their prescribing system contains
all the required details (see PRES-17 above). The requirements in NSW are the same as those for
paper prescriptions with a small number of exceptions. While not required for a paper prescription,
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patient date of birth is required for an electronic prescription. Prescribers of conformant electronic
prescriptions do not need to comply with the following paper prescription requirements:
If a prescribing system does not have a designated field for a required detail (e.g. NSW Authority
number, which is required for certain S8 medicine prescriptions), a prescriber must ensure the detail
is entered into the system so it will be displayed to the dispensing pharmacist. A pharmacist can
dispense an electronic prescription only if all required prescription information is displayed. Contact
your software vendor if you have any concerns or queries about how to enter details in your
prescribing system.
For more information on electronic prescribing visit the Australian Digital Health Agency's Electronic
Prescribing - For Prescribers [https://www.digitalhealth.gov.au/healthcare-providers/initiatives-and-
programs/electronic-prescribing/for-prescribers] .
A pharmacist should not assume that dispensing a prescription is legal merely because the
prescription has been digitally transferred.
Pharmacists who dispense conformant electronic prescriptions are exempted from the requirement
to:
endorse in ink:
the date of dispensing
the pharmacy address
the prescription reference number
the word 'CANCELLED' where no valid repeat supplies remain
Pharmacists are exempted from these requirements because conformant systems record the date of
dispensing, the pharmacy address and the prescription reference number, and securely transmit and
retain details of prescriptions which are easily searchable. Repeats of conformant electronic
prescriptions for S4B and S8 medicines, therefore, do not have to be dispensed at the same pharmacy
which dispensed the original prescription. A patient can take the new token for their repeat
prescription to a different pharmacy if they choose so.
When dispensing electronic prescriptions, pharmacists should be particularly vigilant that the on-
screen display shows repeat intervals where required. A prescription for a S4B or S8 medicine with
repeat/s specified must show an interval for repeats. If no repeat interval appears, directions for any
repeat supplies are invalid and no repeats can be dispensed. The pharmacist may only dispense a
single supply. The prescription should be electronically cancelled to prevent a new token from being
issued.
Pharmacists should also be vigilant that the NSW Authority number is displayed where it is required
(see PRES-17 above). The Authority number must be displayed for a prescription for:
specialist qualification and the words “issued under clause 37 of the Poisons Regulation” or
words to that effect.
For conformant electronic prescriptions for S8 medicines that include all required details, a
pharmacist does not need to contact the prescriber to verify the prescription where the pharmacist
does not know the patient. If a pharmacist has doubt about the identity of the prescriber or any other
aspect of the prescription or the patient’s treatment he/she should contact the prescriber directly.
Validity of tokens
Pharmacists must be confident the token presented by the patient or his/her authorised agent has not
been fraudulently obtained or altered. Where the pharmacist has concerns, the same steps as used
for paper prescriptions are appropriate, including sighting the patient’s or agent’s identification
document/s (e.g. photo driver licence) and/or contacting the prescriber. If the token for a S8 or S4D
prescription has been altered or fraudulently obtained, the electronic prescription should be
cancelled to make the token invalid and unable to be used by any person. The Police should be
informed immediately.
For more information on electronic prescribing visit the Australian Digital Health Agency's Electronic
Prescribing - For Dispensers [https://www.digitalhealth.gov.au/get-started-with-digital-
health/electronic-prescriptions/for-dispensers] .
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