Hierarchy

06Section VI — PRODUCTS OF THE CHEMICAL OR ALLIED INDUSTRIES

3006000000Pharmaceutical goods specified in note|4|to this chapter

3006910000Appliances identifiable for ostomy use 3006920000Waste pharmaceuticals

3006930000Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses

Duties & Measures

Third Country Duty0.000 %

Base rate (erga omnes)

Applies to all third countries without preferential agreement

0.000 %

Preferential rates(19)

Preferential rates - 19 Origin
Origin	Savings	Trade agreement	Details
EU-Switzerland agreement: re-imported goods1007 0.000 %	—	—	2
Preferential origin in accordance with the Agreement in the form of an Exchange of Letters between the European Union and the Kingdom of Morocco on the amendment of Protocols 1 and 4 to the Euro-Mediterranean Agreement establishing an association between the European Communities and their Member States, of the one part, and the Kingdom of Morocco, of the other part.2000 0.000 %	—	—
OCTs2080 0.000 %Overseas Association Decision	—	Overseas Association Decision
Andorra 0.000 %EU-Andorra Customs Union	—	EU-Andorra Customs Union
Switzerland 0.000 %EU-Switzerland Bilateral Agreements	—	EU-Switzerland Bilateral Agreements
Algeria 0.000 %EU-Algeria Association Agreement	—	EU-Algeria Association Agreement
Faroe Islands 0.000 %EU-Faroe Islands FTA	—	EU-Faroe Islands FTA
United Kingdom 0.000 %EU-UK Trade and Cooperation Agreement	—	EU-UK Trade and Cooperation Agreement

Low-value consignment customs duty(2)

inherited from 3000000000

ERGA OMNES

3.000 EURRegulation 0382/262026-07-01

TM01066From 1 July 2026 until 1 July 2028, a customs duty of EUR 3 per item in a consignment the intrinsic value of which does not exceed a total of EUR 150 shall apply instead of the relief eliminated pursuant to Article 1 of this Regulation, where: (a) the importation of the goods is exempt from VAT in accordance with Article 143(1), point (ca), of Directive 2006/112/EC; or (b) the goods are in a postal consignment as defined in Article 1, point (24), of Delegated Regulation (EU) 2015/2446.

ERGA OMNES

3.000 EUR4Regulation 0382/262026-11-01

4 certificate(s) required

C127Other certificates

Merchant product identifier

C128Other certificates

Non-standardised manufacturer product identifier

C129Other certificates

Standardised manufacturer product identifier

Y081Particular provisions

No standardised manufacturer product identifier for the declared product exists

Import not allowed

Import control(2)

inherited from 3000000000

Ukraine

Regulation 0692/142026-06-24

EU-Ukraine DCFTA(since 2016)

3 certificate(s) required

Y997Particular provisions

Goods not originating from or destined to Crimea or Sevastopol (Articles 2 and 2b.1 of Council Regulation (EU) No 692/2014)

N864UN/EDIFACT certificate

Invoice declaration or origin declaration made out by any exporter on invoice or any other commercial document

N954UN/EDIFACT certificate

Movement certificate EUR.1

Import not allowed

CD967I. According to Council Regulation (EU) No 692/2014, it shall be prohibited to import into European Union goods originating in Crimea or Sevastopol. The prohibition shall not apply in respect of goods originating in Crimea or Sevastopol which have been made available to the Ukrainian authorities for examination, for which compliance with the conditions conferring entitlement to preferential origin has been verified and for which a certificate of origin has been issued in accordance with the Association Agreement between the European Union and its Member States, of the one part, and Ukraine, of the other part. II. According to the Council Regulation (EU) 692/2014, the export of goods and technologies suited for use in the sectors of transport; telecommunications; energy; prospection, exploration and production of oil, gas and mineral resources is prohibited: (a) to any natural or legal person, entity or body in Crimea or Sevastopol, or (b) for use in Crimea or Sevastopol.

Ukraine

Regulation 0263/222026-06-24

EU-Ukraine DCFTA(since 2016)

3 certificate(s) required

Y984Particular provisions

Goods not originating from or not destined for the non-government controlled areas of Ukraine in the oblasts of Donetsk, Kherson, Luhansk and Zaporizhzhia

N954UN/EDIFACT certificate

Movement certificate EUR.1

N864UN/EDIFACT certificate

Invoice declaration or origin declaration made out by any exporter on invoice or any other commercial document

Import/export not allowed after control

CD860According to Council Regulation (EU) 2022/263 (OJ L42I, p. 77): I. It shall be prohibited to import into the European Union goods originating in non-government controlled areas of the Donetsk, Kherson, Luhansk and Zaporizhzhia oblasts of Ukraine. The import prohibitions not apply in respect of: (a) the execution until 24 May 2022 of trade contracts concluded before 23 February 2022, or of ancillary contracts necessary for the execution of such contracts, provided that the natural or legal person, entity or body seeking to perform the contract has notified, at least 10 working days in advance, the activity or transaction to the competent authority of the Member State in which they are established; (b) goods originating in the specified territories which have been made available to the Ukrainian authorities for examination, for which compliance with the conditions conferring entitlement to preferential origin has been verified and for which a certificate of origin has been issued in accordance with the EU-Ukraine Association Agreement. II. It shall be prohibited to sell, supply, transfer or export goods and technology listed in Annex II to Council Regulation (EU) 2022/263: (a) to any natural or legal person, entity or body in the specified territories, or (b) for use in the specified territories. Annex II shall include certain goods and technologies suited for use in the following key sectors: (i) transport; (ii) telecommunications; (iii) energy; (iv) the prospecting, exploration and production of oil, gas and mineral resources. The prohibitions in point II above shall be without prejudice to the execution until 24 August 2022 of an obligation arising from a contract concluded before 23 February 2022, or from ancillary contracts necessary for the execution of such contracts, provided that the competent authority has been informed at least five working days in advance.

Import control -fluorinated greenhouse gases(1)

ERGA OMNES

—Regulation 0573/242025-09-17

CD807https://climate.ec.europa.eu/system/files/2024-12/guidance%20customs%20F-gas%20labelling%20medicinal%20products.pdf

CD917By virtue of Article 4(6) of Regulation (EU) 2024/573, the placing on the market of fluorinated greenhouse gases shall be prohibited, unless importers provide evidence that any trifluoromethane, produced as a by-product during the production process of the fluorinated greenhouse gases has been destroyed or recovered for subsequent use, using best available techniques. By virtue of Article 11.1. of Regulation (EU) 2024/573, the placing on the market of products and equipment, including parts thereof, listed in Annex IV, with an exemption for military equipment, shall be prohibited from the date specified in that Annex. By virtue of Article 11.1 sub paragraph 2 (a)(b), (c) of Regulation (I) 2024/573, the placing on the market of parts of products and equipment required for repair and servicing of existing equipment listed in Annex IV shall be allowed. By virtue of Article 11.3. of Regulation (EU) 2024/573, the placing on the market of non-refillable containers for fluorinated greenhouse gases listed in Annex I and in Section 1 of Annex II, empty, or fully or partially filled, shall be prohibited. By virtue of Article 11.4 of Regulation (EU) 2024/573, undertakings which place on the market refillable containers for fluorinated greenhouse gases shall produce a declaration of conformity that includes evidence confirming that there are binding arrangements in place for the return of those containers for the purpose of refilling, in particular identifying the relevant actors, their obligatory commitments and the relevant logistical arrangements. By virtue of Article 12 of Regulation (EU) 2024/573, the following products and equipment that contain fluorinated greenhouse gases or whose functioning relies upon those gases shall only be placed on the market if they are labelled as: (a) refrigeration equipment ; (b) air-conditioning equipment ; (c) heat pumps ; (d) fire protection equipment ; (e) electrical switchgear ; (f) aerosol dispenser that contain fluorinated greenhouse gases, including metered dose inhalers; (g) all fluorinated greenhouse gas containers ; (h) fluorinated greenhouse gas-based solvents ; or (i) organic Rankine cycles. By virtue of Article 16 of Regulation (EU) 2024/573, the placing on the market of hydrofluorocarbons shall be allowed only to the extent that importers have been allocated quota by the Commission as set out in Article 17. By virtue of Article 19.1 of Regulation (EU) 2024/573, refrigeration and air-conditioning equipment, heat pumps and metered dose inhalers pre-charged with substances listed in Section 1 of Annex I shall not be placed on the market unless those substances with which the products or equipment have been pre-charged are accounted for within the quota system. By virtue of Article 19.2 of Regulation (EU) 2024/573, the placing on the market of goods falling under the provisions of Article 19.1 shall be subject to the presentation of a declaration of conformity. By virtue of Article 19.6 of Regulation (EU) 2024/573, undertakings that placed on the market less than 10 tonnes of CO2 equivalent of hydrofluorocarbons, per year, contained in the products or equipment referred to in Article 19.1 shall be exempted from the provisions of Article 19. By virtue of Article 20.4 of Regulation (EU) 2024/573, the undertakings shall have a valid registration in the F-gas Portal prior to carrying out any of the activities listed in points (a) to (g). By virtue of Article 23.3 (a) of Regulation (EU) 2024/573, the F-gas Portal registration identification number shall be declared. The information listed in Article 23.3(a) to (d) of Regulation (EU) 2024/573 shall be provided to customs authorities, where relevant, in the customs declaration.

Import control -REACH(1)

inherited from 3000000000

ERGA OMNES

Regulation 1907/062023-02-10

3 certificate(s) required

Y106Particular provisions

Compliance with the REACH restrictions defined in Column 2 of Annex XVII of Regulation (EC) No 1907/2006

Y110Particular provisions

Exemption from REACH restrictions by virtue of Article 67(1) and 67(2) of Regulation (EC) No 1907/2006

Y113Particular provisions

Substance/mixture not subjected to the provisions of Regulation (EC) No 1907/2006 (Annex XVII)

Import/export not allowed after control

CD730A substance for which Annex XVII contains a restriction shall not be imported unless it complies with the conditions of that restriction. This shall not apply to the manufacture, placing on the market or use of a substance in scientific research and development. Annex XVII shall specify if the restriction shall not apply to product and process orientated research and development, as well as the maximum quantity exempted. The restrictions shall not apply to the use of substances in cosmetic products, as defined by Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products (repealing the Directive 76/768/EEC), with regard to restrictions addressing the risks to human health within the scope of that regulation. (Article 67 points 1 and 2 of Regulation (EC) No 1907/2006).

CHM00009REACH - Annex XVII - Entry 9

Start date: 2022-01-01

Description & Classification

Common misclassifications

3006910000: The goods are identifiable for ostomy use.
3006920000: The goods are waste pharmaceuticals.

Classification tips

The goods are placebos or blinded or double-blinded clinical trial kits for a recognised clinical trial, put up in measured doses.

Typical uses

Placebo

Sample products

Regulatory notes

Chapter noteChapter 30 — Pharmaceutical products

1. This chapter does not cover: (a) foods or beverages (such as dietetic, diabetic or fortified foods, food supplements, tonic beverages and mineral waters), other than nutritional preparations for intravenous administration (Section IV); (b) preparations such as tablets, chewing gum or patches which are intended to help smokers stop smoking (heading 2106 or 3824); (c) plasters specially calcined or finely ground for use in dentistry (heading 2520); (d) aqueous distillates or aqueous solutions of essential oils, suitable for medicinal uses (heading 3301); (e) preparations of headings 3303 to 3307, even if they have therapeutic or prophylactic properties; (f) soap or other products of heading 3401 containing added medicaments; (g) preparations with a basis of plaster for use in dentistry (heading 3407); (h) albumin not prepared for therapeutic or prophylactic uses (heading 3502). 2. For the purposes of heading 3002, 'immunological products' applies when such products are used directly on patients for therapeutic or prophylactic purposes, including monoclonal antibodies (MAbs), antibody fragments, antibody conjugates and antibody fragment conjugates. 3. For the purposes of headings 3003 and 3004, the following are to be treated as: (a) 'unmixed products': unmixed products dissolved in water; all goods of Chapters 28 or 29; and simple vegetable extracts of heading 1302, merely standardised or dissolved in any solvent; (b) 'mixed products': colloidal solutions and suspensions; mixtures obtained from extraction of vegetable substances or of animal substances; and products of Note 3(a) to which substances have been added. 4. Heading 3006 applies only to: sterile surgical catgut and similar sterile suture materials; sterile laminaria and sterile laminaria tents; sterile absorbable surgical or dental haemostatics; opacifying preparations for X-ray examinations and diagnostic reagents designed to be administered to the patient; blood-grouping reagents; dental cements and other dental fillings; bone reconstruction cements; first-aid boxes and kits; chemical contraceptive preparations based on hormones, on other products of heading 2937 or on spermicides; gel preparations designed to be used in human or veterinary medicine as a lubricant for parts of the body for surgical operations or physical examinations or as a coupling agent between the body and medical instruments; pharmaceutical waste.

Non-preferential origin

tariff_shift

-- Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses

CTH

tariff_shift

-- Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses

CTH

Residual rule

Where the country of origin cannot be determined by application of the prima ry rules and the other

Annex 22-01 DA 2015/2446

FAQ

What is the EU customs duty for Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses (3006930000)?

The third country duty (erga omnes) for Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses is 0.000 %. This rate applies to imports from countries without a preferential trade agreement with the EU.

Are there tariff preferences for Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses (3006930000)?

Yes, 16 tariff preferences are available for this code. Preferential rates apply to imports from countries with a trade agreement with the EU.

Are import controls required for Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses (3006930000)?

Yes, 4 import control measure(s) apply to this code (e.g. CITES, REACH, sanitary controls, etc.).

What products are classified under code 3006930000?

TARIC code 3006930000 (Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses) covers the following products: Placebo, put up in measured doses, for a recognised blinded clinical trial, Double-blinded clinical trial kit, put up in measured doses.

Help

Need help?

Ask a question about this code or find a tariff classification expert.

Hierarchy

06Section VI — PRODUCTS OF THE CHEMICAL OR ALLIED INDUSTRIES

3000000000PHARMACEUTICAL PRODUCTS

3006000000Pharmaceutical goods specified in note|4|to this chapter

3006910000Other

3006910000Appliances identifiable for ostomy use 3006920000Waste pharmaceuticals

3006930000Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses

Duties & Measures

Third Country Duty0.000 %

Base rate (erga omnes)

Applies to all third countries without preferential agreement

0.000 %

Preferential rates(19)

Preferential rates - 19 Origin
Origin	Savings	Trade agreement	Details
EU-Switzerland agreement: re-imported goods1007 0.000 %	—	—	2
Preferential origin in accordance with the Agreement in the form of an Exchange of Letters between the European Union and the Kingdom of Morocco on the amendment of Protocols 1 and 4 to the Euro-Mediterranean Agreement establishing an association between the European Communities and their Member States, of the one part, and the Kingdom of Morocco, of the other part.2000 0.000 %	—	—
OCTs2080 0.000 %Overseas Association Decision	—	Overseas Association Decision
Andorra 0.000 %EU-Andorra Customs Union	—	EU-Andorra Customs Union
Switzerland 0.000 %EU-Switzerland Bilateral Agreements	—	EU-Switzerland Bilateral Agreements
Algeria 0.000 %EU-Algeria Association Agreement	—	EU-Algeria Association Agreement
Faroe Islands 0.000 %EU-Faroe Islands FTA	—	EU-Faroe Islands FTA
United Kingdom 0.000 %EU-UK Trade and Cooperation Agreement	—	EU-UK Trade and Cooperation Agreement

Low-value consignment customs duty(2)

inherited from 3000000000

ERGA OMNES

3.000 EURRegulation 0382/262026-07-01

ERGA OMNES

3.000 EUR4Regulation 0382/262026-11-01

4 certificate(s) required

C127Other certificates

Merchant product identifier

C128Other certificates

Non-standardised manufacturer product identifier

C129Other certificates

Standardised manufacturer product identifier

Y081Particular provisions

No standardised manufacturer product identifier for the declared product exists

Import not allowed

Import control(2)

inherited from 3000000000

Ukraine

Regulation 0692/142026-06-24

EU-Ukraine DCFTA(since 2016)

3 certificate(s) required

Y997Particular provisions

Goods not originating from or destined to Crimea or Sevastopol (Articles 2 and 2b.1 of Council Regulation (EU) No 692/2014)

N864UN/EDIFACT certificate

Invoice declaration or origin declaration made out by any exporter on invoice or any other commercial document

N954UN/EDIFACT certificate

Movement certificate EUR.1

Import not allowed

Ukraine

Regulation 0263/222026-06-24

EU-Ukraine DCFTA(since 2016)

3 certificate(s) required

Y984Particular provisions

Goods not originating from or not destined for the non-government controlled areas of Ukraine in the oblasts of Donetsk, Kherson, Luhansk and Zaporizhzhia

N954UN/EDIFACT certificate

Movement certificate EUR.1

N864UN/EDIFACT certificate

Invoice declaration or origin declaration made out by any exporter on invoice or any other commercial document

Import/export not allowed after control

Import control -fluorinated greenhouse gases(1)

ERGA OMNES

—Regulation 0573/242025-09-17

CD807https://climate.ec.europa.eu/system/files/2024-12/guidance%20customs%20F-gas%20labelling%20medicinal%20products.pdf

Import control -REACH(1)

inherited from 3000000000

ERGA OMNES

Regulation 1907/062023-02-10

3 certificate(s) required

Y106Particular provisions

Compliance with the REACH restrictions defined in Column 2 of Annex XVII of Regulation (EC) No 1907/2006

Y110Particular provisions

Exemption from REACH restrictions by virtue of Article 67(1) and 67(2) of Regulation (EC) No 1907/2006

Y113Particular provisions

Substance/mixture not subjected to the provisions of Regulation (EC) No 1907/2006 (Annex XVII)

Import/export not allowed after control

CHM00009REACH - Annex XVII - Entry 9

Start date: 2022-01-01

Trade Statistics

Description & Classification

Common misclassifications

3006910000: The goods are identifiable for ostomy use.
3006920000: The goods are waste pharmaceuticals.

Classification tips

The goods are placebos or blinded or double-blinded clinical trial kits for a recognised clinical trial, put up in measured doses.

Typical uses

Placebo

Sample products

Regulatory notes

Chapter noteChapter 30 — Pharmaceutical products

Non-preferential origin

tariff_shift

-- Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses

CTH

tariff_shift

-- Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses

CTH

Residual rule

Where the country of origin cannot be determined by application of the prima ry rules and the other

Annex 22-01 DA 2015/2446

FAQ

What is the EU customs duty for Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses (3006930000)?

Are there tariff preferences for Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses (3006930000)?

Yes, 16 tariff preferences are available for this code. Preferential rates apply to imports from countries with a trade agreement with the EU.

Are import controls required for Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses (3006930000)?

Yes, 4 import control measure(s) apply to this code (e.g. CITES, REACH, sanitary controls, etc.).

What products are classified under code 3006930000?

Help

Need help?

Ask a question about this code or find a tariff classification expert.

Section noteNotes to Section VI — Products of the chemical or allied industries

1. (A) Products (other than radioactive ores) answering to a description in heading 2844 or 2845 are to be classified in those headings and in no other heading of the Nomenclature. (B) Subject to paragraph (A) above, products answering to a description in heading 2843, 2846 or 2852 are to be classified in those headings and in no other heading of this Section. 2. Subject to Note 1 above, products classifiable in heading 3004, 3005, 3006, 3212, 3303, 3304, 3305, 3306, 3307, 3506, 3707 or 3808 by reason of being put up in measured doses or for retail sale are to be classified in those headings and in no other heading of the Nomenclature. 3. Goods put up in sets consisting of two or more separate constituents, some or all of which fall in this Section and are intended to be mixed together to obtain a product of Section VI or VII, are to be classified in the heading appropriate to that product, provided that the constituents are: (a) having regard to the manner in which they are put up, clearly identifiable as being intended for use together without first being repacked; (b) presented together; and (c) identifiable, whether by their nature or by the relative proportions in which they are present, as being complementary one to another.

What are the non-preferential origin rules for Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses (3006930000)?

Non-preferential origin rules for Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses are defined in Annex 22-01 of the UCC Delegated Act. These rules determine the country of origin for MFN duty rates, trade policy measures, and origin marking.

Can TARIC code 3006930000 be used on a customs declaration?

Yes, TARIC code 3006930000 (Placebos and blinded (or double-blinded) clinical trial kits for a recognised clinical trial, put up in measured doses) is a declarable code. It can be used directly on EU customs import and export declarations (Single Administrative Document).

Trade Statistics

Imports

€0

Exports

€0

Balance

€0

Import €/kg

€2.7K/kg

Export €/kg

€740.03/kg

Market concentration (HHI)

4,244

Concentrated

Trade value (2022–2025)

Import sources

Third-country sourcing partners

#	Partner	Value (EUR)	kg	€/kg	Share
1	🇬🇧 United Kingdom	€1.1B	65Kt	€17.3K/kg	59.0%
2	🇺🇸 United States	€461.2M	367Kt	€1.3K/kg	24.2%
3	🇨🇭 Switzerland	€246.9M	142Kt	€1.7K/kg	13.0%
4	🇨🇦 Canada	€44.5M	34Kt	€1.3K/kg	2.3%
5	🇨🇳 China	€27.7M	16Kt	€1.8K/kg	1.5%

Export markets

Third-country target markets

#	Partner	Value (EUR)	kg	€/kg	Share
1	🇺🇸 United States	€345.2M	206Kt	€1.7K/kg	45.5%
2	🇬🇧 United Kingdom	€185.8M	341Kt	€545.20/kg	24.5%
3	🇨🇳 China	€108.7M	33Kt	€3.3K/kg	14.3%
4	🇨🇭 Switzerland	€61.6M	52Kt	€1.2K/kg	8.1%
5	🇦🇷 Argentina	€56.9M	41Kt	€1.4K/kg	7.5%

EU Member States

EU ImportersEU Exporters

View full analysis

Imports

€0

Exports

€0

Balance

€0

Import €/kg

€2.7K/kg

Export €/kg

€740.03/kg

Market concentration (HHI)

4,244

Concentrated

Trade value (2022–2025)

Import sources

Third-country sourcing partners

#	Partner	Value (EUR)	kg	€/kg	Share
1	🇬🇧 United Kingdom	€1.1B	65Kt	€17.3K/kg	59.0%
2	🇺🇸 United States	€461.2M	367Kt	€1.3K/kg	24.2%
3	🇨🇭 Switzerland	€246.9M	142Kt	€1.7K/kg	13.0%
4	🇨🇦 Canada	€44.5M	34Kt	€1.3K/kg	2.3%
5	🇨🇳 China	€27.7M	16Kt	€1.8K/kg	1.5%

Export markets

Third-country target markets

#	Partner	Value (EUR)	kg	€/kg	Share
1	🇺🇸 United States	€345.2M	206Kt	€1.7K/kg	45.5%
2	🇬🇧 United Kingdom	€185.8M	341Kt	€545.20/kg	24.5%
3	🇨🇳 China	€108.7M	33Kt	€3.3K/kg	14.3%
4	🇨🇭 Switzerland	€61.6M	52Kt	€1.2K/kg	8.1%
5	🇦🇷 Argentina	€56.9M	41Kt	€1.4K/kg	7.5%

EU Member States

EU ImportersEU Exporters

View full analysis