# ISOCONSULT S.R.L. - EU Authorized Representative (Romania)

> ISOCONSULT S.R.L. is a company registered in Romania (EUID ROONRC.J2025030488006) that acts as EU Authorized Representative and GPSR responsible person for manufacturers outside the European Union. The company is certified ISO 9001, ISO 14001 and ISO/IEC 27001.

Key facts:
- Legal name: ISOCONSULT S.R.L.; Romanian tax ID (CUI) 51705731; Trade Register J2025030488006; EUID ROONRC.J2025030488006
- Registered office: Str. Ștefan cel Mare nr. 52, Anexa 1, Sat Independența, Comuna Independența, Județul Galați, România
- Contact: contact@isoconsult-eu.com, +40 763 038 001
- Certifications: ISO 9001, ISO 14001, ISO/IEC 27001
- Services: EU Authorized Representative mandate (Regulation (EU) 2019/1020 Art. 4), GPSR responsible person (Regulation (EU) 2023/988), technical file, EU Declaration of Conformity, CE label approval, lab testing coordination, technical translation
- Prices: technical file setup 600-1,500 EUR per product family (one-off); EU Authorized Representative 1,200-3,500 EUR per year per manufacturer; lab testing at laboratory cost; consultancy and translation 60-100 EUR per hour; VAT excluded where applicable
- Languages of the website: English (primary), Romanian (/ro/), Simplified Chinese (/zh/)

## Services

- [Services](https://isoconsult-eu.com/services/): EU Authorized Representative mandate, GPSR responsible person, technical file, EU Declaration of Conformity, CE label approval, lab testing coordination and technical translation.
- [EU Authorized Representative](https://isoconsult-eu.com/services/eu-authorized-representative/): Appoint ISOCONSULT S.R.L. (Romania) as your EU Authorized Representative under Regulation (EU) 2019/1020. Annual mandate, 10-year technical file archive, authority liaison.
- [GPSR Responsible Person](https://isoconsult-eu.com/services/gpsr-responsible-person/): ISOCONSULT S.R.L. acts as EU responsible person under the General Product Safety Regulation (EU) 2023/988 for non-EU manufacturers and online sellers.
- [Technical File](https://isoconsult-eu.com/services/technical-file/): Complete EU technical documentation for non-EU manufacturers: product description, Declaration of Conformity, test reports, risk assessment, instructions and CE label. One-off setup fee per product family.
- [EU Declaration of Conformity](https://isoconsult-eu.com/services/declaration-of-conformity/): Correct EU Declaration of Conformity for CE-marked products: model structure, applicable directives and regulations, harmonised standards, notified body data, English and Romanian versions.
- [CE Label Approval](https://isoconsult-eu.com/services/label-artwork-approval/): We review product labels and packaging for CE marking, manufacturer and EU Authorized Representative details, traceability codes and mandatory warnings before production.
- [Lab Testing Coordination](https://isoconsult-eu.com/services/lab-testing/): Coordination of product testing with ISO/IEC 17025 accredited laboratories in Romania and the EU, and review of test reports from China. Laboratory fees charged at cost.
- [Technical Translation](https://isoconsult-eu.com/services/technical-translation/): Translation and adaptation of user manuals, safety warnings, technical data sheets and Declarations of Conformity into Romanian and other EU languages.

## CE marking and EU product rules

- [CE Marking](https://isoconsult-eu.com/ce-marking/): Practical CE marking guide: Low Voltage, EMC, RoHS, Radio Equipment, Toys, PPE and General Product Safety Regulation. What each law requires and which documents you need.
- [Low Voltage Directive (LVD)](https://isoconsult-eu.com/ce-marking/lvd/): LVD 2014/35/EU explained for non-EU manufacturers: scope, conformity assessment, harmonised standards, documents and labelling for electrical equipment.
- [EMC Directive](https://isoconsult-eu.com/ce-marking/emc/): Electromagnetic Compatibility Directive 2014/30/EU explained: scope, emission and immunity standards, documentation for electronic products sold in the EU.
- [RoHS Directive](https://isoconsult-eu.com/ce-marking/rohs/): RoHS 2011/65/EU for non-EU manufacturers: 10 restricted substances, limits, technical documentation according to EN IEC 63000 and CE marking.
- [Radio Equipment Directive (RED)](https://isoconsult-eu.com/ce-marking/red/): RED 2014/53/EU explained: safety, EMC, radio spectrum and cybersecurity requirements under Delegated Regulation (EU) 2022/30 for wireless products sold in the EU.
- [Toy Safety](https://isoconsult-eu.com/ce-marking/toys/): CE marking for toys under Directive 2009/48/EC: safety assessment, EN 71 standards, warnings, traceability and documentation for non-EU toy manufacturers.
- [Personal Protective Equipment](https://isoconsult-eu.com/ce-marking/ppe/): CE marking of personal protective equipment under Regulation (EU) 2016/425: risk categories I, II and III, notified body involvement and documentation.
- [General Product Safety (GPSR)](https://isoconsult-eu.com/ce-marking/gpsr/): GPSR 2023/988 for non-EU manufacturers: which products are covered, EU responsible person, technical documentation, labelling and online sales requirements.

## Company

- [How it works](https://isoconsult-eu.com/how-it-works/): Five steps to appoint ISOCONSULT S.R.L. as your EU Authorized Representative: due diligence, technical file review, mandate contract, label approval and 10-year archive.
- [Pricing](https://isoconsult-eu.com/pricing/): Published prices: technical file setup from 600 EUR per product family, EU Authorized Representative mandate from 1,200 EUR per year, lab testing at cost, consultancy 60 to 100 EUR per hour.
- [About us](https://isoconsult-eu.com/about/): ISOCONSULT S.R.L. is a Romanian company certified ISO 9001, ISO 14001 and ISO/IEC 27001, acting as EU Authorized Representative for non-EU manufacturers.
- [Authorities](https://isoconsult-eu.com/authorities/): Official links: ANPC, ANCOM, RENAR, Labour Inspectorate, Romanian Customs, NANDO, Safety Gate and ICSMS. Who checks which products in Romania and the EU.
- [FAQ](https://isoconsult-eu.com/faq/): Answers to the questions non-EU manufacturers ask most about EU Authorized Representatives, CE marking, GPSR, technical files, labels and prices.
- [Contact](https://isoconsult-eu.com/contact/): Request a quote for EU Authorized Representative services, technical file review or CE label approval. Reply within one business day.
- [Company information](https://isoconsult-eu.com/legal/company-information/): Legal and registration details of ISOCONSULT S.R.L.: registered office, tax ID, Trade Register number, EUID and contact.

## Articles

- [EU Authorized Representative vs Importer vs Responsible Person: Who Does What?](https://isoconsult-eu.com/blog/eu-authorized-representative-vs-importer/): Non-EU manufacturers often confuse the importer, the Authorized Representative and the GPSR responsible person. Here is how the roles differ under EU law and which one you need.
- [GPSR for Non-EU Manufacturers and Sellers: What Changed and What You Must Do](https://isoconsult-eu.com/blog/gpsr-requirements-for-non-eu-sellers/): The General Product Safety Regulation (EU) 2023/988 applies since 13 December 2024. A practical checklist for manufacturers and online sellers from outside the EU.
- [The CE Technical File: The 6 Documents EU Authorities Expect](https://isoconsult-eu.com/blog/ce-technical-file-six-documents/): What a complete EU technical file contains, the mistakes we see most often in files from non-EU manufacturers, and how to prepare yours before an inspection.

## FAQ

Q: What is an EU Authorized Representative?
A: A natural or legal person established in the EU who has a written mandate from a non-EU manufacturer to carry out specified tasks on its behalf, such as keeping the Declaration of Conformity and technical documentation available to authorities and cooperating with them.

Q: Do manufacturers from China need an EU representative?
A: Yes, in most cases. Article 4 of Regulation (EU) 2019/1020 requires an economic operator established in the EU for products such as electrical equipment, electronics, radio equipment, toys and PPE. Since December 2024, the General Product Safety Regulation extends this to consumer products in general. If you have no EU importer taking that role, you need an Authorized Representative.

Q: What is the difference between an importer and an Authorized Representative?
A: An importer buys the goods and places them on the EU market in its own name, with its own legal obligations. An Authorized Representative does not buy or sell the goods: it acts for the manufacturer under a written mandate. You can sell through any distributors while ISOCONSULT acts as your representative.

Q: Is a representative in Romania valid for sales in Germany, France or other EU countries?
A: Yes. The requirement is an operator established in the European Union. ISOCONSULT S.R.L. is established in Romania and can represent you for products sold anywhere in the EU.

Q: Can ISOCONSULT issue a CE certificate?
A: No. CE marking is affixed by the manufacturer after the conformity assessment. For most products no third party is involved. Where a notified body is required, for example for PPE category II and III, we help you find one and check its certificate. ISOCONSULT is not a notified body.

Q: Are test reports from Chinese laboratories accepted?
A: They can be, if the laboratory is accredited to ISO/IEC 17025 for the standards tested, the standards are current, and the tested model matches your product. We check each report and tell you if additional testing is needed.

Q: What must be printed on the label?
A: Depending on the product: CE marking, manufacturer name and postal address, the EU operator's name and contact details, a type, batch or serial number, and the required warnings and symbols. Consumer information must be in the language of the country of sale.

Q: How long do you keep our documents?
A: 10 years after the last product covered by the mandate is placed on the market, as required by EU legislation. This obligation continues even if the contract ends.

Q: What happens if an authority contacts you?
A: We inform you immediately, provide the requested documents within the legal deadline, usually 10 to 15 working days, and cooperate on any corrective action. That is why we need your technical file up to date at all times.

Q: How long does the setup take?
A: It depends on the quality of your documents. When the technical file is complete, the review and contract usually take about two weeks. If testing is needed, the laboratory timeline is added.

Q: Can you be our responsible person on Amazon and other marketplaces?
A: Yes. Once the mandate is active, we provide the EU responsible person details required by GPSR for your online listings.

Q: Which languages do you work in?
A: We work in English and Romanian. Chinese-language documents and correspondence are handled through translation.

Q: What if a product turns out to be unsafe?
A: We inform you and, where the law requires it, the authorities, and we cooperate on corrective measures. If a manufacturer breaches the contract, for example by changing a product without notice, we may suspend or terminate the mandate and notify the authorities.