Policy collection

Medicine Policies for CQC Registered Care Services

Medicine policies decide how safely a service handles the most common source of avoidable harm in social care, which is why every regulated provider needs them written properly rather than downloaded and edited at the last minute. This collection brings together the medicine policies a service uses every day: medicines management, administration and recording, controlled drugs, covert administration, as required medication, homely remedies, self-administration, and medication errors and near misses. We write each one for your service, so your registered company name, your Care Quality Commission provider and location identifiers, your registered manager and your named medicines lead appear in the text instead of a blank waiting to be filled. A person reads every document before it is sent. You receive it within two working days, print-ready on your own letterhead, with a sign-off block ready for signature. Buy a single policy or the whole set as a one-time purchase, with no subscription and no quote needed. CareStream made these for managers who want a document that holds up when somebody reads it closely. 

6 in this collectionWritten for your service, not a templateChecked against the law before it carries your name
Medicines Management Policy

Ordering, storage, administration, recording and disposal of medicines, including errors and self-administration.

£794 regulations
Controlled Drugs Policy

Receipt, storage, administration, recording and destruction of controlled drugs.

£693 regulations
Consent to Care and Treatment Policy

Seeking, recording and reviewing consent, including where capacity fluctuates.

£693 regulations
Clinical Governance Policy

How clinical quality is led, measured, audited and improved.

£693 regulations
Safe Care and Treatment Policy

The Regulation 12 umbrella: risk assessment, safe premises, medicines and infection prevention brought together.

£691 regulation
Care Planning Policy

Person-centred assessment, planning, review and involvement under Regulations 9 and 12.

£692 regulations

Policies your staff can follow, and your inspector can read, available to buy one at a time

Medicines sit under the Safe key question of the Care Quality Commission's Single Assessment Framework, in the quality statement on medicines optimisation. That is the practical reason this collection exists. When an inspector looks at how your service handles medicines, they are checking whether what is written down matches what happens on the floor, whether the document reflects the law as it stands today, and whether your staff can explain the process in their own words. A generic template cannot do that job, because it does not know who your medicines lead is, whether you hold controlled drugs, or whether your staff administer in a care home or in somebody's own kitchen. Each document here is written against your service profile, priced openly, and delivered as a finished document rather than a form to complete.

What a medicines policy is and which regulations it answers to

A medicines policy is the written statement of how your service orders, receives, stores, administers, records, transfers and disposes of medication, and who is accountable at each step. It answers directly to Regulation 12 of the Health and Social Care Act 2008 (Regulated Activities) Regulations 2014, which requires the proper and safe management of medicines as part of safe care and treatment, and to Regulation 17 on good governance, which requires accurate, complete and contemporaneous records. Where medication is given to somebody who cannot consent, the Mental Capacity Act 2005 applies. Where controlled drugs are held, the Misuse of Drugs Regulations 2001 set the storage, register and destruction requirements. Good practice is drawn from the National Institute for Health and Care Excellence guidance on managing medicines in care homes and for adults receiving social care in the community. Your policy should name all of this, not gesture at it.

Which medicine policies your service has to hold

There is no single statutory list, and the honest answer depends on what you do. A residential care home that administers from a monitored dosage system needs a medicines management policy, an administration and recording policy covering the Medication Administration Record, a policy on as required medication with individual protocols, a homely remedies policy, and one on errors and near misses. A nursing home holding Schedule 2 controlled drugs needs a controlled drugs policy with register, balance check and destruction arrangements. A domiciliary care agency needs a policy that distinguishes prompting, assisting and administering, because that distinction decides what your staff may lawfully do in somebody's home. Supported living services need a self-administration and capacity policy that starts from independence. Hospices need anticipatory and subcutaneous medication covered. Buy only what applies to you.

What is inside each document, from controlled drugs to homely remedies

Every document in this collection follows the same shape. It opens with scope and purpose, naming your service and setting, then states the regulation and guidance it answers to, then sets out the procedure step by step in the order your staff actually work through it. It names roles rather than people where roles are what matter, and names people where accountability requires it, including your registered manager, nominated individual and medicines lead. It covers recording, what a gap on a Medication Administration Record means and how it is investigated, what happens when a dose is refused, missed or given in error, when the prescriber is contacted, when a safeguarding referral is made, and how duty of candour applies. It ends with review date, version number, approval and a sign-off block for your letterhead.

Who these policy products are perfect for

These are made for the registered manager, owner or nominated individual of a small CQC registered service running one or two locations without a compliance department behind them. You know your service, and you know your regulations. What you do not have is a spare afternoon to rewrite a medicines policy from a template that still says insert name here, or a reason to buy a nine hundred pound pack when what you were asked for was one document. People buy from this collection at particular moments: an inspection booked or just finished, a report that named medicines as an area for improvement, a registration application or a new regulated activity, a local authority or integrated care board contract asking for evidence, a medication error that exposed a gap, or a new manager inheriting a folder nobody has opened in three years.

Written for your service, hand-checked, and updated when the law changes

Personalisation here means something specific rather than a merge field in a header. Before a document is written, we take your registered company name and trading name, your address, your Care Quality Commission provider identifier and location identifier, your registered manager and nominated individual, your regulated activities and your setting type. Those details are merged into the body of the text, so the policy reads as your service's own document from the first page. It is then checked against the regulations that apply to your setting rather than the sector in general, and read by a person before it reaches you. You get it within two working days, print-ready, with nothing left to complete except signatures.

Why our policies are better than free templates and nine hundred pound packs

Compare what you are actually holding. A free template is written for nobody, so it names no one accountable and cites regulations that may have moved. A large pack sold on subscription gives you nineteen documents you did not need in order to get the one you did, and bills you again next year. A consultant will write you something good and charge a day rate to send a file. What CareStream sells sits between those: one document, written for your service, human-reviewed, with the regulation named in full and the people named by role and name. When the law changes, we update the wording and tell you what moved, so your version does not quietly date. No policy can promise an inspection outcome, and we will not pretend otherwise. What it can do is stand up to being read carefully.

Prices, one-time purchase and secure checkout, with no subscription

Prices are on the page, because you should not have to ask. A single policy from this collection is £39 to £79 depending on length and complexity, so a homely remedies policy sits at the lower end and a full medicines management policy at the upper. A themed bundle covering the medicines documents a setting usually holds together is £295. The twenty statutory documents every CQC-registered service is expected to hold, medicines included, are £495. All of it is a one-time purchase through secure checkout, with no contract and no subscription, and nobody you have to speak to first. If the document is not right, tell us, and we will put it right or refund it in full under our return policy. Get started by choosing the document you were asked for.

How these documents connect to the rest of your policy set

Medicines documents are rarely bought alone, and inspectors rarely read them alone. They sit alongside your infection prevention and control policy, your safeguarding adults policy, your consent and mental capacity policy and your record keeping policy, all of which are available in the full library of care policies written for CQC registered services. A written policy also has to be matched by staff who can show they understood it, which is why most services pair this collection with medication administration and competency training for care staff. If you support people in their own homes, the medicines documents you need differ in scope from a care home's, and the setting-specific guidance on policies and procedures for domiciliary care agencies explains where those differences fall. Every document you buy is also held in your CareStream account, so the version you approved is the version your staff see.

Medicine Policies for CQC Registered Care Services FAQs

What is a medicines policy in a care service?

It is the written statement of how your service handles medication from ordering through to disposal, and who is accountable at each step. It covers storage, administration, recording on the Medication Administration Record, refusals, errors, transfers between settings and disposal. It is the document an inspector asks for when looking at the medicines optimisation quality statement, and the document your staff should be able to describe in their own words.

Which medicines policies do I need for CQC registration?

For a registration application, you would normally hold a medicines management policy covering ordering, storage, administration and disposal, plus a medication errors and near misses policy. If you will hold controlled drugs, add a controlled drugs policy. If you will administer to people who lack capacity, add a covert administration policy. The Care Quality Commission does not publish a fixed list, so the correct set follows from the regulated activities you have applied for.

Which medicine policies does a domiciliary care agency have to have?

A domiciliary care agency needs a policy that clearly separates prompting, assisting and administering, because that distinction governs what a care worker may lawfully do in somebody's home. It should also cover what happens when a visit is missed, how the Medication Administration Record is completed in the home, how medicines are stored by the person rather than the agency, and how errors are reported when nobody else is present.

What are the ten golden rules of medication administration?

There are no official ten golden rules issued by the Care Quality Commission or any English regulator. The phrase circulates in nursing education and varies by source. Rather than adopting somebody else's numbered list, a policy that will hold up sets out your own checks: identity, prescription, dose, route, timing, capacity and consent, recording, and what to do when any of those cannot be confirmed.

What are the key points of the Medicines Act 1968?

The Medicines Act 1968 created the licensing system for medicines in the United Kingdom and set the three legal categories under which medicines are supplied. Much of its licensing detail was later replaced by the Human Medicines Regulations 2012, which is now the main source for the supply and sale of medicines. For a care service, the practical inheritance of the Act is the category system and the rules on who may supply what.

Policies are one part of it.

CareStream is the compliance system underneath: your policies, your staff training, your audits and your evidence, kept current and ready for the day somebody asks to see them.

  • Policies written and kept updated for you
  • Staff training that records itself against the standard
  • Gap analysis showing what you are missing before an inspector does
  • Everything in one place, for one price

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