Process

What a consultation must cover before a cosmetic procedure

What a cosmetic consultation is required to cover in the UK: who must assess you, what must be disclosed, and why a sales appointment is not a consultation.

Checks before you agree· Reviewed 2026-08-01·Published by Northbank Media
Institutional architecture, flat daylight. Documentary imagery only: this publication does not use treatment photography.
Institutional architecture, flat daylight. Documentary imagery only: this publication does not use treatment photography.
The short answer

A consultation before a cosmetic procedure should be carried out by the person who will perform it, should establish why you want it and whether it is appropriate for you, and must cover what the procedure involves, its realistic outcome, its risks and complications, the alternatives including doing nothing, what happens if you are unhappy, and the cost of any correction. Professional guidance from the GMC and other regulators treats consent as a process rather than a signature, and a meeting whose purpose is to close a sale is not a consultation.

The word consultation does an enormous amount of work in cosmetic advertising. It is used for everything from a proper clinical assessment by the person who will treat you, through to a fifteen minute appointment with a non clinical adviser whose job title is consultant and whose actual role is sales. The two are not related. Knowing which one you have been booked into is one of the more consequential things you can work out in advance.

Who should be doing it

The person who assesses you should be the person who will perform the procedure. This sounds obvious. It is routinely not what happens. In a model that has become common, a patient is assessed and sold to by one person, and treated on the day by another, sometimes meeting the treating practitioner for the first time minutes before the needle.

Professional guidance is clear on the principle. The GMC's guidance for doctors carrying out cosmetic interventions places responsibility for the consent discussion on the doctor performing the intervention, and says it must not be delegated. Similar expectations run through the standards of the other healthcare regulators. Where the person injecting you is not a registered healthcare professional at all, no regulator's guidance binds them, and you are relying entirely on their own standards.

CheckpointTest the appointment you have been offered
Ask who will carry out the consultationIf it is not the person who will perform the procedure, ask why, and ask when you will meet the person who will.
Ask whether the person consulting you is clinically qualifiedPatient adviser, treatment coordinator and consultant are job titles, not clinical registrations.
Ask what would make them decline to treat youA practitioner who cannot describe a case they would turn down is describing a sales process.
Ask what a complication would cost youCorrection, reversal and follow up. Get the answer before the deposit, not after the swelling.
Ask for the written information to take awayIf there is nothing to take away, there is nothing to reflect on.
If the answer is not thisIf the assessment and the treatment are the same appointment, and nobody offers you time, walk away.

Why you want it, and whether it is appropriate

A real consultation starts with you rather than the treatment menu. It asks what is prompting this, what you expect to change, whether the concern you are describing is actually addressed by the procedure being discussed, and whether there is anything in your medical history, your medication, your expectations or your circumstances that makes it a poor idea now.

Regulatory guidance in this area asks clinicians to consider psychological vulnerability, including whether a patient may have body dysmorphic disorder, and to be prepared to decline to treat. A consultation that is incapable of ending in the word no is not a consultation. If every path through the appointment leads to a booking, the appointment was never an assessment.

What must be covered

Whatever the setting, the following has to be on the table before you can meaningfully agree to anything.

  • What the procedure actually is, in plain language, including the product or drug class used and what it does in the body.
  • What result is realistic for you, as distinct from what is achievable for someone else.
  • The risks and complications, including the rare but serious ones, and what would be done about each.
  • The alternatives, including less invasive options and the option of doing nothing at all.
  • How long it lasts, whether it is reversible, and what happens as it wears off.
  • Recovery, downtime, and what is normal in the days afterwards as opposed to what is not.
  • Who to contact out of hours, and how fast they respond.
  • What a correction or a complication costs, and who pays for it.
  • The total price, including any follow up, and what is not included.

The last two are where a great many consultations quietly fail. The cost of the treatment is discussed enthusiastically. The cost of putting it right is not discussed at all.

Your rights

What you are entitled to at this stage

  • To be assessed by the person who will perform the procedure, and to have the consent discussion with them.
  • To be told the risks that would matter to you, not a generic list, and to have your own circumstances taken into account.
  • To be offered the alternatives, including the alternative of doing nothing.
  • To be given the price of correcting a poor result before you agree to the procedure.
  • To take the information away and decide later, without penalty or pressure.

Consent is a process. A signature at the end of it records the process. It cannot replace it.

Risk has to be personalised, not recited

The legal standard for what must be disclosed shifted decisively with the Supreme Court's decision in Montgomery v Lanarkshire Health Board in 2015. The test is no longer what a responsible body of clinicians would have disclosed. It is whether a reasonable person in the patient's position would attach significance to the risk, or whether the clinician should reasonably be aware that this particular patient would.

Applied to cosmetic work, that has a practical consequence. If your job, your hobby, your event next month or your particular anxiety makes a specific outcome significant to you, the discussion has to engage with that, not with a laminated list. A consultation that recites generic risks and never asks what matters to you is not meeting the standard.

Red flag

A consultation that ends with a signature on a consent form you were given for the first time that minute, in the treatment room, with the product already drawn up, has inverted the process. The form is meant to record a discussion that already happened.

Time between the discussion and the needle

There is no single statutory cooling off period for cosmetic procedures across the UK, and anyone who tells you otherwise is oversimplifying. What exists is professional guidance that expects patients to be given time to reflect, and consumer law that in some circumstances gives cancellation rights for contracts made at a distance or away from business premises. We set out how those interact in our guide to cooling off.

The practical point stands regardless of the law. If you were assessed and treated in the same appointment, you did not have time to reflect, and no form saying you did changes that.

What you should leave with

You should leave a consultation with written information about the procedure, a note of what was discussed including the risks, a clear price, and the name and registration of the person who will treat you. If a prescription only medicine is involved, you should know who is prescribing it and whether they have assessed you in person. That is covered in our guide to remote prescribing.

You should not leave with a deposit paid on a treatment you have not had time to think about, a finance agreement signed in the room, or a discount that expires before you could reasonably reflect. Those are sales devices, and their presence in a clinical appointment tells you what the appointment was for.

What a good consultation feels like

It is slower than you expect. It spends more time on your history than on the product. It names at least one thing that could go wrong in enough detail to be uncomfortable. It offers doing nothing as a real option rather than a rhetorical one. It gives you a price that includes the unglamorous parts. And it ends without a booking, because the practitioner assumes you will want to think.

If that description sounds unlike the appointment you have been offered, that is worth knowing before you go, not afterwards.

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This article contains no commercial links of any kind. No affiliate links, no sponsored placements, and no links to any clinic, practitioner, brand, product or retailer. Nobody paid for it, nobody previewed it and nobody outside the editorial team saw it before publication.

This publication does not name, rank, rate or review any clinic or practitioner, because it has assessed none of them. Our funding is set out in full on the about page and in our editorial standards.

Nothing here is medical or legal advice. Speak to a qualified clinician about your own circumstances, and to a solicitor about a claim.

Sources

We cite regulators, legislation and clinical institutions, and we link them so you can check the current position yourself. We do not link to clinics or retailers. Regulation in this field changes, so the primary source is always better than our summary of it.

Frequently asked questions

Does the person who treats me have to be the person who consults me?

Professional guidance for doctors is explicit that responsibility for the consent discussion sits with the doctor performing the intervention and should not be delegated, and comparable expectations apply across the other healthcare regulators. Where the injector is not a registered professional, no regulator's guidance applies to them at all.

Is a signed consent form proof that I consented?

It is evidence that a form was signed. Valid consent depends on whether you were given the information a reasonable person in your position would want, had capacity, and agreed voluntarily. A form signed minutes before treatment, with no prior discussion, is weak evidence of any of that.

How long should a cosmetic consultation take?

There is no fixed time. What matters is whether it covered your history, your motivation, realistic outcomes, risks, alternatives, complication costs and who to contact. If all of that happened properly, it was not brief.

Can a clinic refuse to treat me?

Yes, and a willingness to do so is a good sign. Professional guidance expects clinicians to decline where a procedure is not in the patient's interests, where expectations are unrealistic, or where there are signs of psychological vulnerability such as body dysmorphic disorder.

What if I was only offered a phone or video consultation?

Remote assessment can be reasonable for information gathering, but for procedures involving prescription only medicines the prescriber is expected to have an adequate assessment of you, and prescribing for injectables without a face to face assessment has been criticised by regulators. Ask specifically who is prescribing and whether they will see you.

When the rules change, we will tell you

One email when a law or a regulator's guidance changes in a way that alters what you should check, and when a new article is published. No treatment offers, no product recommendations and no clinic suggestions, because we do not make any.

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