New Course
DATES 22nd October 2024
Start Times
13:00 hrs
Finish Times
16:00 hrs
Location
UK - Webinar
Fee
*Early bird discounted course fee/attendee = £280.
[*Applies for up to 10 days prior to the scheduled course date]
Full fee/attendee = £350.
Toxicology Basics - Intermediate (13:00 - 16:00 hrs)m
This is a great follow-on course to the highly popular ‘Toxicology Basics – Introductory’ training course.
This live training webinar picks up from the ”Toxicology Basics – Introductory’ training course in that it looks in more detail at adverse and non adverse effects, testing strategies (alternatives and in vivo), including the purpose of controls and satellite groups, vehicles, group sizes, selection of doses and choice of exposure routes.
It will also look at how simple physicochemical properties can be used in the determination of likely exposure routes. The weight of evidence concept, adaptations and data waivers will also be covered.
Furthermore, this course will also look at the basic concepts of statistical significance, biological and toxicological significance. Sources of data and its reliability (Klimisch ratings) and, whether or not it should be used will also be covered. Examples will be provided throughout the session to illustrate key points.
It is a great training course for you to deepen your knowledge of toxicology – REACH, CLP/GHS, SDS, COSMETIC REGS, BIOCIDES -BPR,etc.
It 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 Regulation, etc. It will also be useful for those of you involved with writing safety data sheets (SDS) and classification and labelling (CLP/GHS)
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By attending this training course you will gain an understanding of,
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The use of data waivers, adaptation and weight of evidence in regulatory toxicology.
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Data sources and assessment of reliability – i.e. should I use this data?
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The differences between adverse and non adverse effects.
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How to use simple physicochemical properties for the assessment of potential exposure routes.
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The underlying principles regarding the assessment of toxicity – including alternatives and in vivo approaches.
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The importance of control groups, satellite groups, choice of appropriate vehicles, group sizes, dose selection and appropriate exposure routes.
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What is meant by statistical significance, biological and toxicological significance.
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- This training course 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).
- It is perfect for anyone who wants to deepen their knowledge of toxicology!
- Training notes complementing the webinar
- Copy of all slides used during the training
- Copy of the live recording
- Certificate of attendance (if required)
- You can also ask questions at any time during or after the training webinar class
Laura holds an MSc in Applied Toxicology, a BSc (Hons) Chemistry, PgC Occupational Hygiene and PGCE Post Compulsory Teaching Qualification.
She has worked for many years in industry working in product stewardship which includes writing safety data sheets, classification and labelling, regulatory submissions and workplace risk assessments. She is an experienced trainer and a published author.
Her recent book ‘A Practical Guide to Toxicology and Human Health Risk Assessment (John Wiley & Sons, December 2018)
Testimonials
Unable to attend the scheduled date/time of webinar?
Please contact me if you are unable to attend a scheduled date/time of a webinar and we can schedule one-off dates/times to suit.
This is particularly useful if you are based on the west coast of the USA/Canada or Asia-Pacific region where the timings of the webinars might be inconvenient!