Standard operating procedure

Prescribing & Medicines Management Procedure

The step-by-step procedure for safely prescribing, obtaining, storing, administering and disposing of medicines in an aesthetic clinic.

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  • Editable Microsoft Word (.docx)
  • Mapped to the CQC standards
  • Optional 3-monthly updates

What's inside

This standard operating procedure is fully drafted and structured, ready to brand and complete for your service. It covers:

  • 1. Purpose
  • 2. Scope
  • 3. Definitions and abbreviations
  • 4. Responsibilities
  • 5. Equipment and materials
  • 6. Procedure
  • 7. Documentation
  • 8. Records
  • 9. Related documents
  • 10. Review and version control
  • 11. Disclaimer

Legislation & standards it maps to

  • Human Medicines Regulations 2012 (in particular Regulation 214 - sale or supply of prescription-only medicines)
  • Health and Social Care Act 2008 (Regulated Activities) Regulations 2014 - Regulation 12 (Safe care and treatment)
  • Misuse of Drugs Act 1971 and Misuse of Drugs Regulations 2001 (where controlled drugs are held)
  • Medicines and Healthcare products Regulatory Agency (MHRA) Yellow Card scheme

Who it applies to

All independent prescribers, practitioners, registered nurses and support staff who prescribe, order, store, handle, administer or dispose of medicines at [Organisation Name].

Glossary

Plain-English explanations of the technical terms and legislation used in this document.

Adrenaline (epinephrine)
The emergency medicine given by injection to treat a severe, life-threatening allergic reaction (anaphylaxis).
Adverse drug reaction (ADR)
An unwanted or harmful reaction that follows the use of a medicine.
Aseptic non-touch technique
A method of preparing and giving injections that avoids touching the parts that must stay sterile, so the medicine does not become contaminated.
Botulinum toxin
A prescription-only medicine injected to relax muscles, commonly used in aesthetic treatments to soften lines and wrinkles.
Care Quality Commission (CQC)
The independent regulator of health and social care services in England.
Cold chain
Keeping vaccines and certain medicines within a safe temperature range from delivery through to use.
Contemporaneous record
A record made at the time an action happens, or as soon as possible afterwards, so it is accurate and reliable.
Contraindication
A reason, such as a health condition or another medicine, why a particular treatment should not be given to a person.
Controlled drug
A medicine whose supply, storage and records are tightly restricted by law because of its potential for misuse.
Dermal filler
A gel-like substance injected beneath the skin to smooth lines or add volume; an adjunct is a product used alongside it.
Falsified medicine
A fake medicine that has been deliberately mislabelled about its identity, source or history.
Health and Social Care Act 2008 (Regulated Activities) Regulations 2014
The regulations setting the fundamental standards that providers of regulated care must meet, including Regulation 12 on safe care and treatment.
Human Medicines Regulations 2012
The main law in the United Kingdom governing how medicines for human use are licensed, supplied and administered.
Hyaluronidase
An injectable medicine used to dissolve dermal filler, including in an emergency such as a blocked blood vessel.
Independent prescriber
A doctor, dentist or other suitably qualified and registered professional who can assess a patient and prescribe medicines on their own responsibility.
Informed consent
Agreement to treatment given freely after the risks, benefits and alternatives have been clearly explained.
Local anaesthetic
A medicine that numbs a small area of the body so a procedure can be carried out without pain.
Medicines and Healthcare products Regulatory Agency (MHRA)
The body that regulates medicines and medical devices in the United Kingdom and runs the Yellow Card reporting scheme.
Misuse of Drugs Act 1971 and Misuse of Drugs Regulations 2001
The laws that control how controlled drugs may be stored, supplied, recorded and disposed of.
Near miss
An event that could have caused harm but did not, either by chance or because it was caught in time.
Off-label use
Using a licensed medicine in a way not covered by its official approval, for example for a different purpose or dose.
Patient Group Direction (PGD)
A written instruction letting named staff supply or give a medicine to a group of patients without an individual prescription.
Patient-specific direction
A written instruction from a prescriber to give a named medicine to a named, individually assessed patient.
Pharmacy (P) medicine
A medicine that can be sold only from a pharmacy under a pharmacist's supervision, without a prescription.
Prescription-only medicine (POM)
A medicine that may lawfully be supplied only on the instruction of an appropriate prescriber.
Quarantine (of stock)
Setting a product aside and clearly marking it as not for use until a decision is made about it.
Reconstitution
Mixing a medicine that comes as a powder with a liquid to make it ready to inject.
Registered Manager
The person registered with the regulator as responsible for the day-to-day running of a service.
Regulated activity
A type of care or treatment the law requires a provider to register with the regulator to deliver.
Remote prescribing
Prescribing a medicine without seeing the patient face to face, for example by telephone, video or online form.
Sharps
Needles, blades and other items that can cut or puncture the skin.
Standard Operating Procedure (SOP)
A written, step-by-step instruction for carrying out a routine task safely and consistently.
Stock rotation (first to expire, first out)
Arranging stock so that the items due to expire soonest are used first, to reduce waste.
Summary of Product Characteristics (SmPC)
The manufacturer's official, licensed information about a medicine, including how to use it safely.
Wholesale dealer
A licensed business that buys and supplies medicines in bulk to clinics, pharmacies and other authorised buyers.
Yellow Card scheme
The Medicines and Healthcare products Regulatory Agency's system for reporting suspected side effects and defective medicines.

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  3. Complete the placeholders for your service, then have it approved before use.
  4. Add the optional updates subscription and we keep it current as guidance changes.

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