Auxilife Newsletter

Amendment to the New Drugs and Clinical Trial Rules (2023)  Scientists and researchers empowered to explore alternative testing methods, reducing reliance on animal experimentation.   The amendment empowers scientists and researchers to explore alternative testing techniques such as in vitro studies, computer simulations, and other...

Health Canada’s Pest Management Regulatory Agency (PMRA) has released a comprehensive five-year work plan outlining its re-evaluation and special review activities ‘up to March 31, 2028’. The purpose of this plan is to inform registrants, pesticide regulatory officials, and the Canadian public about the agency’s...

PFAS (per- and polyfluoroalkyl substances) represent a large class of synthetic chemicals with extensive use. The proposal was prepared by authorities in Denmark, Germany, the Netherlands, Norway and Sweden then submitted it to ECHA. Aim of the PFAS restriction proposal is to reduce PFAS emissions...

European union has announced and adopted the regulation (EC) No. 1069/2009 regarding the usage of animal by-products in fertilizer products on dated 30th May 2023. Aim of this updation is to lay down public health and animal health rules for animal by-products. To ensure the...

This is exciting news for the assessment world! Software tool DROPLET has been developed by the Dutch Board for the Authorisation of Plant Protection Products and Biocides (Ctgb) to assess whether pesticides in Dutch surface water abstraction points for drinking water production may exceed the...

European Food Safety Authority (EFSA) has announced the release of its updated guidance document for assessing risks to honeybees, bumble bees and solitary bees from plant protection products. This new guidance document has been revised to incorporate the latest scientific knowledge and cutting-edge methodologies for...

ECHA launched the public consultation on formaldehyde released from the reaction products of paraformaldehyde and 2-hydroxypropylamine. If an active substance meets any of the criteria listed in Article 10(1) of the BPR, the evaluating competent authority may identify it as a potential candidate for substitution...

The BPR requires the evaluation of active substances contained in biocidal products, as well as the evaluation of the products themselves before they can be placed on the EU market. Member States of the EU are responsible for evaluating the active substances and biocidal products...

It has been announced that the European Commission has amended Annex I of Regulation (EC) No 1272/2008 to add hazard classes to the classification, labelling, and packaging of substances and mixtures and to introduce new classification criteria to identify endocrine disrupting chemicals (EDCs) and persistent...