On October 21, from 17:00 to 18:00 CEST, Costanza Rovida will be the presenter of a free webinar organized by American Society for Cellular and Computational Toxicology.
TEAM mastery will attend the Annual Biocontrol Industry Meeting, the premier global meeting for the biocontrol industry and is internationally recognized as the global platform for the industry to network, discover and unveil new products, market opportunities and research areas.
TEAM mastery S.r.l. will participate to the OpenTox Virtual Conference 2021, a four-day virtual global meeting for a safer world. The event will take place online from 20 to 24 September.
TEAM mastery will participate at the Biocides Europe 2019 conference dedicated to the latest developments of the BPR.
TEAM mastery will attend ABIM – the global biocontrol industry meeting. THE CONTEXT The Annual Biocontrol Industry Meeting (ABIM) is a joint project of the International Biocontrol Manufacturers Association (IBMA) and the Research Institute of Organic Agriculture (FiBL). ABIM is…
TEAM mastery and Centro Reach are promoting the constitution of a Task Force on Quaternary Ammonium Salts and are inviting companies to attend the event that will take place at “Auditorium of Federchimica” located in Via Giovanni da Procida, 11, Milan…
TEAM mastery is proud to be the ”event sponsor” of EUROTOX 2019 that will be held in Helsinki from the 8th to the 11th of September.
On July 22nd, a draft modification of Annex VIII of the CLP was published by the European Commission for the public consultation phase. ANNEX VIII CLP: WHAT IS GOING TO CHANGE The most representative changes are the following: 1. Postponement…
Secondo il Regolamento REACH (1907/2006) si definisce sostanza intermedia: una sostanza fabbricata, consumata o utilizzata per essere trasformata, mediante un processo chimico, in un’altra sostanza. Il REACH ha poi ulteriormente distinto tre tipologie di intermedi: Non isolati Isolati in sito…
Con l’entrata in vigore del Regolamento EU 745/2017 (MDR), che avrà piena e inderogabile applicazione a partire dal 26 maggio 2020, le aziende produttrici di dispositivi medici devono considerare tempi e modi per adeguarsi ai cambiamenti regolatori previsti. Alla base del nuovo…