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Switzerland · Responsible person and agent

Sell cosmetics in Switzerland.

A Swiss-address responsible person for your products, with your file retained for ten years, as your partner for the Swiss market.

Swiss-address responsible person File kept for ten years Fixed transparent pricing
Swiss market scene, brand products with an Alpine backdrop

What the law requires

What the Swiss market requires.

Switzerland sits outside the EU and runs its own cosmetics rules. EU compliance does not carry across the Swiss border on its own. To sell a cosmetic in Switzerland, your brand must meet Swiss requirements directly.

Reviewed by Cassandra Maddocks, chemist & biochemist · last reviewed 26 July 2026

Switzerland requires a responsible person with a Swiss-territory address and a self-monitoring dossier kept ten years for cantonal inspection; there is no notification portal. Warnings must appear in at least one of German, French or Italian. CIG provides the Swiss address, holds the file and checks the labels.

Legal basis: Fedlex: Swiss Cosmetics Ordinance (VKos), EUR-Lex: Regulation (EC) 1223/2009.

The Swiss requirement is separate from the EU one, so a brand selling in both markets needs cover in each. They fit together in one relationship, but they are two obligations.

What Switzerland requires
A responsible person or agent with an address on Swiss territory.
A Product Information File, retained and available for ten years.
Swiss safety and labelling requirements met for each product.

The Swiss regime, in plain terms

Swiss cosmetics rules sit under the Federal Act on Foodstuffs and Utility Articles (817.0) and the Ordinance on Foodstuffs and Utility Articles. The instrument that governs cosmetics directly is Ordinance 817.023.331, the Ordinance on Cosmetic Products. Article 54 of the wider framework requires cosmetics to comply with the annexes of EU Regulation 1223/2009, so the prohibited-ingredient, colourant and preservative lists that apply in the EU also apply in Switzerland. The formulation rules line up closely with the EU. The compliance structure around them does not.

A Swiss-address responsible person, held on Swiss territory

The responsible person for the Swiss market can be the manufacturer, the importer, or an appointed agent, but that person or entity must have an address on Swiss territory. An importer or distributor may appoint an authorised representative in writing, provided that representative holds a Swiss address. The Swiss meaning of the role differs from the EU one. In Switzerland the responsible person is the contact point for the surveillance authorities and must be a physical person. If a brand does not designate anyone, the role does not simply lapse: the company’s CEO or equivalent legal representative assumes it by default, wherever they are based. For a foreign brand, that is usually unintended personal exposure rather than a deliberate choice.

An EU Responsible Person does not satisfy this requirement. An EU address may be printed on the packaging, but the legal obligation cannot be delegated to it or to anyone located abroad. Swiss authorities have no access to the EU CPNP database and cannot read your EU notification. The obligation has to sit inside Switzerland.

No pre-market notification: control is by cantonal inspection

Switzerland has no notification portal and no pre-market registration step. There is no Swiss equivalent of CPNP or SCPN, and nothing to submit before a product goes on sale. Instead, control happens after the product is on the market. Cantonal enforcement laboratories, working across the 26 cantons, carry out post-market inspections and can request your compliance data at any time. Because inspections are unannounced, the practical obligation is to hold a complete, current self-monitoring dossier ready to hand over on request, rather than to file anything up front.

The Product Information File and its ten-year clock

Each product needs a Product Information File that an inspector can be given on request. The file must be kept for ten years from the date the last batch was first placed on the market, and it has to stay available to the authorities for that whole period. A Product Information File already compiled abroad, for example an EU file, can satisfy the Swiss requirement if it meets Swiss cosmetics and labelling rules. It may be written in an official Swiss language or in English. The underlying safety work still has to be there: a safety assessment signed by a qualified assessor, a manufacturing method with a GMP statement to ISO 22716, stability and microbiological data, and support for any claim the label makes.

Labelling and Swiss language rules

Warnings and instructions for use must appear in at least one official Swiss language, meaning German, French, or Italian. EU or UK claim approvals do not carry across automatically, so packaging that is compliant for an EU shelf is not automatically compliant for a Swiss one. Switzerland also diverges from the EU on some technical points. It regulates chemicals under its own Chemical Risk Reduction Ordinance (ORRChem) rather than REACH, and it prohibits furocoumarins at or above 1 mg/kg in products intended for sun exposure. Products lawfully marketed in the EU can enter Switzerland under the Cassis de Dijon principle without reformulation, provided they still meet the supplementary Swiss requirements and are not on the published negative list.

Enforcement and who carries the risk

Enforcement is the job of the cantonal laboratories, exercised through post-market inspection rather than an approval gate. In practice the liability tends to land on the Swiss importer, who by default holds the Product Information File. A foreign brand without its own Swiss entity depends on that importer or on a paid agent, which complicates control of the dossier if the importer relationship changes. Appointing your own Swiss agent keeps the file and the named contact under your control rather than tied to a single distributor.

How CIG covers it

Your Swiss compliance, handled for you.

CIG acts as your Swiss responsible person and agent. We give your products the required Swiss address, hold your Product Information File for the full ten years, and handle contact with Swiss authorities on your behalf. As your range grows and the rules change, we keep your Swiss compliance current.

We act as your Swiss responsible person and agent.
We give your products the required Swiss address.
We hold your Product Information File and retain it for the full ten years.
We act as your point of contact for Swiss authorities.
We keep your Swiss compliance current as your range and the rules change.
Product Information File, a printed dossier with a signed safety report

How it works, step by step

From first email to a Swiss shelf.

Because Switzerland has no notification portal, the work is about building a complete file and putting a named Swiss contact behind it, then keeping both ready for inspection. Here is the order it runs in.

1

Submit your products

Send us your product list, formulas with full INCI, existing safety reports, current labels, and where the products are made. We tell you which of these already meet Swiss rules and what is still missing.

2

Receive a fixed quote

You get a fixed price and a timeline for Swiss coverage before any work starts. If you also need the EU, UK, or US, the quote covers those markets in the same document.

3

We build or check the file

We assemble the Product Information File to Swiss requirements or check an existing EU file against them. Where a signed safety report is needed, a qualified assessor prepares and signs it.

4

We fix the label

We review your label and claims for Swiss rules, including warnings in an official Swiss language, and tell you exactly what to change before the product ships.

5

We become your Swiss contact

We take on the responsible person and agent role with a Swiss address, and we hold your file for the full ten-year retention period.

6

Ready for inspection

Your dossier stays current and available to the cantonal laboratories. If an inspector asks for it, the complete file is already in place, and we handle the exchange.

Realistic timelines

How long this takes depends almost entirely on the state of your paperwork, not on any filing queue, because there is nothing to file. When your safety reports, formulas, and labels are already in order and only need checking against Swiss rules, appointing the Swiss agent and confirming the file is a matter of a short onboarding window. When a product still needs a signed safety assessment, or the underlying stability and microbiological testing has not been done, that testing sets the pace. Stability testing in particular can run for months, and no responsible person can compress it. The honest planning rule is to start Swiss coverage well before your intended launch, and to treat any missing lab work as the long pole in the schedule rather than the compliance paperwork itself.

Why products get pulled here

What goes wrong for first-timers.

Swiss control happens after a product is already on sale, so problems surface during an inspection rather than at a submission screen. These are the recurring reasons a foreign brand gets caught out.

Relying on the EU Responsible Person. The most common assumption is that an EU address on the pack covers Switzerland. It does not. With no Swiss-address responsible person appointed, the CEO becomes the responsible person by default, and there is no local contact for the authorities.
No self-monitoring dossier ready. Because nothing is filed up front, brands assume there is nothing to hold. When a cantonal laboratory asks for the file, an incomplete or missing Product Information File is exactly what triggers a finding.
An incomplete Product Information File. A missing signed safety assessment, absent stability or microbiological data, or no GMP statement to ISO 22716 leaves the file unable to stand up to inspection.
Warnings not in a Swiss language. Labels that carry warnings and instructions only in English fail the requirement to use at least one of German, French, or Italian. EU-compliant packaging is not automatically Swiss-compliant.
An unauthorised or restricted ingredient. Switzerland applies the EU annexes plus its own points of divergence, for example the furocoumarin limit in sun-exposure products. A formula that passes elsewhere can still breach a Swiss rule.
Unsupported claims. A claim on the label with no evidence behind it in the file is a recurring weakness that inspectors flag.
Losing control of the file through the importer. When the importer holds the Product Information File by default, a change of importer can leave a brand without access to its own dossier at the moment an inspector asks for it.
What we need from you
Your product list and the intended Swiss launch date.
Full formulas with INCI names for each product.
Any existing safety reports and Product Information Files.
Current label and packaging artwork, front and back.
The country of manufacture and manufacturing details.
A statement of the claims you want to make on each product.
What CIG delivers
A responsible person and agent with an address on Swiss territory.
A Product Information File built or checked to Swiss requirements.
A safety report signed by a qualified assessor where one is needed.
A label and claims review against Swiss language and content rules.
Your file held and kept available for the full ten-year period.
A named Swiss contact for the cantonal authorities and inspections.

Why CIG

Why brands choose CIG for Switzerland.

Swiss agent of record

Your responsible person sits in Switzerland, with a real Swiss address behind the role.

Fits with EU access

We cover Switzerland alongside the EU for brands selling in both markets.

Fixed, transparent pricing

Published prices, with a fixed quote before any work begins.

Four markets, one partner

Switzerland covered alongside the EU, UK and US, from a single relationship.

FAQ

Common questions about selling in Switzerland.

You need a separate Swiss one. Switzerland is not part of the EU, has its own rules, and its authorities have no access to the EU CPNP database. An EU address may be printed on your pack, but the compliance obligation cannot be delegated to it or to anyone located abroad. The role must sit with a manufacturer, importer, or appointed agent that has an address on Swiss territory.

By default, your company’s CEO or equivalent legal representative. In Switzerland the responsible person must be a physical person, and if none is designated the role falls onto the person legally representing the company, wherever they are based. For a foreign brand that is unintended personal exposure. Appointing a Swiss agent gives the authorities a named local contact instead.

No. Switzerland has no pre-market notification and no portal to submit to, so there is no Swiss version of CPNP or SCPN. Control happens after the product is on the market. Cantonal enforcement laboratories carry out inspections and can ask for your compliance data at any time, so the real obligation is to hold a complete, current file ready to hand over rather than to file anything up front.

Often, yes. A Product Information File compiled abroad, including an EU file, can satisfy the Swiss requirement if it meets Swiss cosmetics and labelling rules. It may be written in an official Swiss language or in English. We check your EU file against Swiss requirements and tell you exactly what, if anything, needs to be added or changed before it is fit for a Swiss inspection.

Warnings and instructions for use must appear in at least one official Swiss language: German, French, or Italian. EU or UK claim approvals do not carry across automatically, so packaging that is compliant for an EU shelf is not automatically compliant for a Swiss one. We review your label against the Swiss rules and set out the changes before the product ships.

Ten years from the date the last batch was first placed on the market. The file has to stay available to the authorities for that whole period. When we act as your Swiss agent, we hold the file and keep it available for the full ten years so it is ready whenever an inspector asks for it.

Inspections are post-market and can be unannounced. A cantonal laboratory can request your compliance data, which means your Product Information File: the product description, the signed safety assessment, the manufacturing method with a GMP statement, stability and microbiological data, and support for the claims on the label. As your named Swiss contact, we hold the current file and handle the exchange with the authorities on your behalf.

It depends on the state of your paperwork, not on any filing queue, because there is nothing to file. When your safety reports, formulas, and labels are already in order and only need checking against Swiss rules, appointing the agent and confirming the file is a short onboarding window. When a product still needs a signed safety assessment or the underlying lab testing has not been done, that testing sets the pace. Stability testing in particular can run for months, so start Swiss coverage well before your intended launch.

Switzerland runs its own tax and chemicals regimes, including its own VAT and a fee on certain volatile organic compounds that has no EU equivalent, so a product priced for the EU may carry Swiss-specific costs on top. Rates change, so confirm the current figures with your tax adviser or importer. Our fee for Swiss compliance is separate and fixed: you get a set price and a timeline before any work begins.

You get a fixed quote before any work starts, and our prices are published. A Product Information File is 400 dollars per product, a signed safety assessment is 450 to 600 dollars per product, and a label and claims review is 300 dollars per product. If you also need the EU, UK, or US, those markets appear on the same quote. See the pricing page for the full list.

Yes, and that is a reason to appoint your own agent. By default the Swiss importer holds the Product Information File, so a change of importer can leave a brand without access to its own dossier at the moment an inspector asks for it. When CIG holds the file as your Swiss agent, the file and the named contact stay with you rather than tied to one distributor.

We cover all four markets: the EU, the UK, Switzerland, and the US under MoCRA. Switzerland is a separate obligation from the EU, but a brand selling in both can hold them in one relationship. Tell us the markets you are entering and we quote them together, so you are not stitching together a separate vendor for each.

Ready to sell in Switzerland?

Tell us your products and we will quote your Swiss coverage at a fixed price.

In practice

Compliance, in the real world.

Swiss pharmacy cosmetics shelf in alpine light
Swiss Authorised Representative paperworkProduct with German and French labelling