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Medicines optimisation

Last quality assured: 15/06/2026
6-minute read

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Last reviewed: 15/06/2026

Medicines optimisation

Medicines optimisation

A female nurse talking to a man and his partner

This resource provides guidance and clinical support for nurses and other healthcare professionals on medicines matters in relation to prescribing and administration of medicines by non-medical healthcare professionals.

What is medicines optimisation?

Medicines optimisation, is a person-centered approach to the safe and effective use of medicines that ensures people obtain the best possible outcomes (NICE, 2015). This approach goes beyond traditional medicines management by focusing on shared decision making, evidence based prescribing, and supporting individuals to use their medicines in a way that maximises benefit and minimises harm.

Good medicines optimisation is a fundamental aspect of nursing and midwifery practice. It encompasses the safe administration of medicines, appropriate prescribing, and supporting people to use their medicines effectively. A medicines optimisation approach places the person at the centre of care, ensuring treatment is better targeted and individuals are better informed, ultimately helping them achieve the best possible outcomes from their medicines.

Medicine supply and administration

Good medicines management is an integral part of most nursing and midwifery practice and includes the administration of medicines, prescribing and supporting people to take their medicines correctly.

All medicines are classified according to three legal categories which are:

  • Prescription-Only Medicines (POM): Must be sold or supplied according to a prescription prescribed by an appropriately qualified health practitioner, this can be a doctor, dentist, or other independent or supplementary prescriber. They can generally only be supplied at a registered pharmacy premises by or under the supervision of a pharmacist.
  • Pharmacy (P) Medicines: Can generally only be sold or supplied at a registered pharmacy premises by or under the supervision of a pharmacist.
  • General Sales List (GSL) medicines: Can be sold from a wider range of premises such as supermarkets as long as those premises can be closed to exclude the public (i.e. they are lockable) and the medicines are pre-packed.

The legislation on medicines regulation is clearly defined under the Human Medicines Regulations 2012. Prescription only medicines (POMs) cannot be administered or supplied unless one of four types of instruction is in place:

  • a signed prescription
  • a signed Patient Specific Direction (PSD)
  • a Patient Group Direction (PGD)
  • a Vaccine Group Direction (VGD).

There are some specific exemptions in medicines legislation which may apply in limited circumstances, for example:

  • The administration of certain parenteral medicines such as adrenaline that can be administered in an emergency without the directions of a prescriber.
  • In occupational health settings, the legislation allows for the supply and/or administration of medicines specified in a written instruction signed by a medical practitioner.

The Specialist Pharmacy Service website outlines the key legal frameworks that govern how medicines can be supplied and administered, along with guidance to help determine the most appropriate mechanism for different situations.

For medicines optimisation in social care settings, there are several resources that outline the standards, requirements, and good‑practice expectations for safe and effective medicines management.

NICE Guideline – Managing Medicines in Care Homes (SC1)

This guideline sets out the national evidence‑based standards for how medicines should be handled in care homes. It covers the full medicines pathway and is the primary reference for providers, managers, and staff.

CQC – Adult Social Care Medicines Resources

The Care Quality Commission provides practical guidance on what “good” looks like when they inspect medicines management in adult social care services.

Regulation 12 (Safe Care and Treatment): What providers must do to ensure medicines are handled safely, including risk assessments, storage, and administration.

Regulation 17 (Good Governance): Requirements for accurate records, audits, and oversight of medicines systems.

Inspection expectations: What inspectors look for during visits, including MAR chart quality, stock control, PRN protocols, and controlled drugs management.

This resource helps providers understand how CQC assesses medicines safety and what is required to meet regulatory standards.

Further resources

RCN

Royal Pharmaceutical Society (RPS)

  • RPS Designated Prescribing Practitioner Competency Framework. This new framework will help universities running independent prescribing programmes, NHS trusts and boards with independent prescribers, trainee independent prescribers and experienced independent prescribers to understand the expectations for a DPP through standardised competency descriptors.
  • RPS. A Competency Framework for all Prescribers. This framework sets out what good prescribing looks like. It describes the demonstrable knowledge, skills, characteristics, qualities and behaviours for a safe and effective prescribing role.

NICE

Further resources

Further developments and feedback

If you have any queries on this guidance or suggestions as to how the guidance can be further developed please contact kim.ball@rcn.org.uk, Professional Lead for Primary Care.

Resource lead(s)

Contact details for the resource lead(s):

K

Kim

Ball

Professional Lead for Primary Care

Last quality assured: 15/06/2026
6-minute read
Last updated date 17/06/2026