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About company

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NewChem OÜ is an innovative organization that offers services in various areas of the chemical industry and scientific activities. The main focus of the company is the correct solution of the problems that are always inherent in the input of any production process. As well as compiling the necessary documentation for the sale and production of your products. Our specialists have more than 15 years of experience in various fields. We are innovative because no one else offers a complex of similar services in one place. And also over the years of work, our specialists have developed their own vision of how to organize a cheap and efficient process and not engage in red tape that no one needs at all.

Do you want to sell a new product in Europe, but do not know which group it belongs to and what documents are required? Consult with us. We will help!

Our services

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Regulation (EC) No 1272/2008 - classification, labeling and packaging of substances and mixtures:

  • Advice on CLP regulations
  • Preparation of security postparts according to GHS, GOST, CLP
  • Registration at the Poison Center, according to CLP ANNEX VIII
  • UFI generation
  • Drawing up a label or control of the drawn up label
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Regulation (EC) No 2019/1020 of the European Parliament and of the Council of 20 June 2019 on detergents:

  • Labeling according to regulation 2019/1020
  • Existing label control, according to regulation 2019/1020
  • Advising on regulation 2019/1020
  • Creation digital passport according regulation 2019/1020
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Regulation (EC) No 1223/2009 of the European Parliament and of the Council of 30 November 2009 on cosmetic products:

  • Advice on regulation 1223/2009
  • Preparation of PIF, SAFETY REPORT in accordance with regulation 1223/2009
  • CPNP registration
  • Drawing up a label or control of the label drawn up in accordance with regulation 1223/2009
  • Testing of cosmetic products
  • Responsible person services for your cosmetic products
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Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017

On medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC

  • Advising on regulation 2017/745
  • Classification of a medical device
  • Registration with EUDAMED
  • UDI generation
  • Drawing up a label or control of the drawn up label, according to regulation 2017/745
  • Drawing up a technical file in accordance with regulation 2017/745
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Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012:

Concerning the making available on the market and use of biocidal products (labeling and control, registration, tests).

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Other services

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EU Ecolabel

Documentation at any stage of the application, recipe control, tests.

Nordic Swan

Documentation at any stage of the application, recipe control, tests.

Eco Right Way

Documentation at any stage of the application, recipe control, tests.

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Consultation

Do you want to organize production? Do you have questions that are not answered? Then this consultation is for you.
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Search and calculation of equipment

Do you know what you want, but do not know where to get the equipment for the production of your product? We will help you choose the best and inexpensive.
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Compilation of recipes and search for raw materials

Do you want to improve the formulation of your product or create a completely new product? We will help you realize your idea.
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Organization of production

You imagine what you want, but do not understand how to organize and implement it in practice? We will help you, at minimal cost, to get the desired result.

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