Responsible Person for Cosmetics in the EU: obligations, labels, notifications and compliance for importers If you want to import cosmetics into the EU, having a good formula and attractive packaging is not enough. Before placing a cosmetic product on the European market, you must make sure it complies with EU rules. One of the most […]
PCN notification in the case of contract manufacturing: the EC Regulation no. 1272/2008 (CLP) states that importers and downstream users of hazardous mixtures shall notify the information specified in Annex VIII to poison control centers through ECHA (European Chemicals Agency). What are the obligations relating to notification to poison centers (PCN notification) and the UFI […]
Is your biocide compliant? If not, are you ready to pay a fine? It was published in official gazette the Legislative Decree n. 179 of 2 November 2021, Discipline of sanctions for the violation of the provisions of Regulation (EU) no. 528/2012 (BPR) relating to the making available on the market and use of biocidal […]
Selling chemicals in Australia requires compliance with applicable regulations. In Australia, there are several rules within which chemical products may fall, whatever the sector of destination (professional, industrial or for the consumer). In general, placing chemicals on the Australian market requires: – compliance with the Industrial Chemicals (Notification and Assessment) Act 1989 of both the […]
In Italian official Journal n. 78 of March 31, 2021, the decree of December 28, 2020 for the notification of dangerous mixtures was published. The decree amends Annex XI of Legislative Decree no. 65 of March 14, 2003, confirming the notification procedures introduced by Annex VIII to european CLP regulation. The notifications must be sent […]
The health emergency triggered by the spread of COVID-19 has clearly highlighted the importance of disinfectant products, which from a regulatory point of view can be Surgical medical devices (PMC) or biocides depending on the active ingredient contained. The companies that, in unsuspected times, had authorized products with virucidal, bactericidal, yeast-containing claims, etc. they had […]
On June 26, the regulation (EU) 2020/878 was published in the European Official Journal, which modifies Annex II of REACH (requirements for the compilation of safety data sheets) and who will apply from January 1, 2021. The change concerns the nanoforms , the endocrine disruptors , L’ inclusion of the UFI ( unique formula identifier […]
Is it true that to deal with safety data sheets in a company you must have followed a qualification course and have a UNI certification? This short article on the SDS manager wants to be a loud reasoning to understand if it is necessary to certify according to UNI / PdR 60: 2019 to carry […]
On November 14, 2020, the two regulations amending the CLP Regulation for harmonized notifications entered into force. With the Delegated Regulation (EU) 2020/1677, Annex VIII of the CLP is further amended, offering both sectoral and intersectoral solutions. The Delegated Regulation (EU) 2020/1676, on the other hand, modifies article 25 of the CLP regulation by specifying […]
By surgical medical devices (PMC) we mean products disinfectants, insecticides, rat poisons and insect repellents containing an active substance under review (not yet included in the European list). PMCs can be placed on the Italian market following registration with the Ministry of Health pursuant to Presidential Decree no. 392 of 6 October 1998 and the […]