Introduction to Regulatory Toxicology and Toxicity Testing ** NEW COURSE **

24th October 2019

Available times: 1000hrs – 1200hrs (UK time) OR 1400hrs – 1600hrs (UK time)

As this is a new course I am offering an early bird fee (until 30th September 2019): £ 170/attendee

Please reserve your place with an email to: [email protected]  
or call Laura on +44 (0)7985 923707   Or book directly here: Online Booking

 

About Introduction to Regulatory Toxicology and Toxicity Testing

This new training webinar class will take an introductory look at regulatory toxicology and the type of toxicity testing which is required. It is a very good follow on course to the Toxicology for Non-Toxicologists training webinar class.

This new webinar is designed in such a way that the information will be useful for a wide variety of industries/regulations e.g. REACH Regulation, Biocides (BPR), Cosmetics, etc. It will also be useful for those of you involved with writing safety data sheets (SDS) and classification and labelling (CLP/GHS).

This training webinar will cover aspects such as data waiving, exposure-based waiving, adaptation, the weight of evidence and read across (and how these can be used with examples). We will also look at sources of data and its reliability (Klimisch ratings) and, whether or not it should be used.

During this two – hour session we will also look at the toxicological endpoints and the current testing methods available (human data, QSAR, physicochemical properties, in vitro and in vivo data) and the regulatory approach to their evaluation/interpretation & use.

This includes acute toxicity (oral, dermal, inhalation), skin/eye/respiratory tract irritation/corrosion, respiratory and skin sensitisation, carcinogenicity, mutagenicity and toxic for reproduction (CMR) and also repeated dose toxicity (target organ toxicity).

Unfortunately, as this is only a two-hour webinar class, it will not give you a university degree in toxicology/regulatory toxicology, but it will help you understand the approach that is taken to testing, its interpretation and the rationale behind it!

Who should attend?

    • Technical/scientific staff who work in a regulatory department
    • Authors of safety data sheets (SDS) and/or extended safety data sheets (eSDS)
    • Staff involved in classification and labelling under EU CLP/ GHS

“I recently attended the Toxicology for Non-Toxicologists course. Laura was an  excellent trainer. Very knowledgeable but explains the subject very well to ensure that those non-technically trained, would understand. Would highly recommend”. Kirsty Ostle – Managing Director Advena Medical Ltd

Training resources included:

  •     Training handbook complementing the webinar
    • Copy of all slides used during the training
    • Copy of the live recording
    • Attendance on the two- hour live training course
    • Certificate of attendance (if required)
    • You can also ask questions at any time during or after the training webinar class

24th October 2019

Available times: 1000hrs – 1200hrs (UK time) OR 1400hrs – 1600hrs (UK time) As this is a new course I am offering an early bird fee (until 30th September 2019): £ 170/attendee

Please reserve your place with an email to: [email protected]  
or call Laura on +44 (0)7985 923707   Or book directly here: Online Booking