(1) A person who applies for a licence under section 14(3) of the Act must develop a quality assurance plan which complies with subregulation (2).
(2) A quality assurance plan must include provisions in relation to the following matters—
(a) infection control;
(b) active clinical monitoring of patients;
(c) management of critical incidents;
(d) management of deteriorating patients;
(e) staff qualifications and training, assessment of qualifications and maintenance of the currency of qualifications;
(f) staff competencies and their maintenance and assessment by a registered training organisation;
(g) recognition of prior learning and overseas qualifications of staff providing clinical care and advice;
(h) access to clinical advice for crew members;
(i) drug security, including storage, use, disposal and records;
(j) manual handling of patients;
(k) patient records;
(l) transportation of personal belongings, including mobility devices;
(m) complaints management;
(n) clinical handover processes;
(o) vehicle equipment;
(p) vehicle crewing;
(q) vehicle and equipment maintenance;
(r) records of all maintenance and repairs to vehicles and equipment;
(s) vehicle and equipment cleaning;
(t) complaints register;
(u) process for investigating complaints.
Reg. 29(3) inserted by S.R. No. 148/2021 reg. 16(2).
(3) A quality assurance plan must be accredited by an accreditation body.
Reg. 30 amended by S.R. No. 148/2021 reg. 17.