Please, send us your e-mail free to receive information about news.

eFirma Doradztwo i Szkolenia
ul. Jasna 18A/19
87-800 Włocławek

phone: +48 605 328 922


eFirma Consulting and Training in order to provide its clients a comprehensive range of services, desiring to assist in fulfilling the obligations imposed on manufacturers, distributors, importers of substances and mixtures, and downstream users.

In our offer you will find services for the safe use of chemicals:

1.  REACH – implementation, consultancy and auditing for the registration of substances, their status, responsibilities, communication between the various participants in the supply chain, and a mandatory provision of information to the European Chemicals Agency (ECHA)

  • Needs analysis and assessment of current business, pre-audit and develop a timetable of activities
  • The role of companies in the supply chain of activities, define the obligations of the company under Regulation (EC) No 1907/2006 REACH, develop a list of substances manufactured, imported and chemicals used in your company require registration proper, who and when should it be made
  • Assistance in interpreting the provisions of REACH, preparing letters, assessment responsibilities of the company and its documentation
    • Ongoing consultations and support for companies at every stage, audits of suppliers, manufacturers, assist in the interpretation of legislative requirements, as the company is to cope with new responsibilities in the light of the EU and national co-operation with regulatory bodies
    • Assistance to manufacturers, importers of the substance at the full registration, prepare and submit the registration dossier, chemical safety assessment, the development of chemical safety report and exposure scenarios for specific applications
    • Support for downstream users who use chemicals in the manufacture of its products, the purification process or for other purposes. If the supplier of the substance does not register it for specific applications relevant to downstream users, it can register itself (exposure scenario developed for the application, complete the necessary documentation)
    • Assistance for the implementation of requirements and obligations under the REACH Regulation on the following issues: information ECHA in Helsinki on quantitative changes in the production or import, new information about the substances, preparation of documents relating to the safe marketing and use of chemicals, registration obligations (updated registration dossier) , completing and complementing the information and documents related to the production and marketing of hazardous chemicals and REACH imposed by national legislation
  •  Notification to ECHA SVHC in articles in accordance with Article. 7.2 REACH
  • Consultations on the implementation of the necessary laboratory tests and an indication of GLP / GLP in Europe, offers help in the selection of laboratories
  • Negotiations on your behalf or represent you as a representative within the Information Exchange Fora (SIEF) for sharing data, sharing the costs of research, joint registration
  • Evaluation of the PBT (persistent, bioaccumulative and toxic) and vPvB (very persistent and having a very bioaccumulative)

2. Safety Data Sheets/SDS

  •  Development of Material Safety Data Sheet / SDS for substances, mixtures, and biocidal products, pesticides, cosmetics based on the recipe
  • The Polish translation from the original data sheet/SDS manufacturer
  • Updated according to Regulation (EC) No 1907/2006 (REACH) Regulation (EC) No 1272/2008 (CLP), Regulation (EC) No 453/2010, Regulation (EC) No 2015/830

3. Classification, labelling of packages, labels, according to CLP

4.  Information Data Sheets, Technical Specifications

  • Notification of new classification and to ECHA in accordance with the CLP
  • Development of the classification, labeling and package / label and packaging of substances and mixtures in accordance with the CLP
  • Development of technical documentation as a form of promotion, leaflet, part of the directory information of each company – use it to the company should present a property, the parameters of its product and reach out effectively described in summary form to customer, translating in English on request

5.  Consultancy ADR

  • Introduction of procedures supervising activities related to the preparation, dispatch and transport of dangerous goods
  • Monitoring compliance of these measures with the requirements of the ADR and the law on road transport of dangerous goods

6.  NIH attests, certificates and technical recommendations

  •  Preparing the necessary documentation to the National Institute of Health (NIH) – if a company wants to sell your product to consumers, to participate in the tenders should have a certificate issued by the NIH National Health Fund, National Institute of Hygiene – information on the recommendations and use a product
  • Preparation of necessary documents and commissioned to perform additional research to obtain certificates, certificates, technical recommendations, as well as contacts with certification bodies (ITB, IBDiM, PCBiC, etc.)

7.  Registration dossiers for biocidal products

  • Preparation of documentation required for registration of biocidal products to the Office for Registration of Medicinal Products, Medical Devices and Biocides (URPLWMiPB)

This is a mandatory requirement for products classified as biocides in accordance with the accordance with the Act on Biocidal Products and Regulation (EU) No 528/2012 completed permitting the marketing of the biocidal product according to national procedure or European procedure

8.  Expertises, opinions interpretation

The development and interpretation of legislation, and help you implement them in the company, according to the profile of activity, according to their individual needs.
9. Training

  • Consulting about the latest regulations, requirements, responsibilities of individual participants in the chain dostawKlasyfikacja and labeling of chemicals according to CLP
  • Workshop preparation Safety Data Sheets for substances and mixtures according to new regulations
  • Assessment of the risks posed by chemicals to human health and the environment and risk management company in the chemical industry
  • Safety and health (OSH) in the company in the chemical industry
  • Preparing professionals to carry out chemical safety assessments, compile reports, data sheets and exposure scenarios

10.  Quality Management Systems according to ISO 9000 standards – implementation, consultancy and audits

ISO 9000 series consists of the following standards:

  • ISO 9000 – Basic information and terminology: the presentation of concepts and management systems used in the industry terminology
  • ISO 9001 – Requirements: identify the criteria that must be met in order to adapt to the assumptions of standards and certification. ISO 9001 is only one part of a series of standards for quality management systems. It helps organizations in the use of what is best in them, enabling them to achieve adequate knowledge related to the process of delivering products and services to customers
  • ISO 9004 – Tips for increasing effectiveness: based on eight principles of quality management information for senior executives, which is structured to enable organizations to achieve higher levels of efficiency by taking into account the needs of all stakeholders, not only to customer requirements.

11.  Environmental Management System ISO 14001 – implementation, consultancy and audits in policy development and environmental objectives, taking into account the requirements and regulations and information about significant environmental impacts

12.  Management System Occupational Health and Safety according to OHSAS 18001 PN-N – implementation, consultancy and audits in policy development and goals of health and safety, taking into account the requirements and regulations and information about significant impacts on the health and safety

13.  Food Safety Management System ISO 22000 – implementation, consultancy and HACCP audits on safety, quality of food (including supplements), cosmetics and medicinal products

  • Needs analysis and assessment of current business, pre-audit and develop a timetable of activities
  • Elaboration of Good Hygiene Practice (GHP) and Good Manufacturing Practice (GMP), HACCP books, design according to the standards BRC, IFS, procedures and instructions, to determine corrective actions.