Toxicological Risk Assessment & Product Safety Forum
About the event
The Toxicological Risk Assessment & Product Safety Forum is a brand new event from Chemical Watch and Chemical Risk Manager. It will focus on how countries are evaluating risk, and ensuring safe products - such as personal care/consumer products, food and medical devices - are put into the market.
This event promises to be the first-of-its kind in Asia Pacific. Bringing together over 15 experts in global chemical risk assessment and regulation, from industry, agencies and professional organisations, this one-day practical conference will include presentations, round table discussions and interactive Q&A sessions to raise awareness and standards of Risk Assessment and Products Safety in Asia Pacific.
Speakers at the conference include key industry stakeholders, regulatory toxicologists from agencies in the EU (including European regulators), Asia Pacific, and ACTRA (Australasian College of Toxicology and Risk Assessment). They will cover a wide range of topics, including food, consumer products, personal care products, chemicals (including biocides and pesticides) and therapeutic goods/life science products.
There will also be updates from Singapore, Malaysia, South Korea, Thailand, Australia and Japan, along with an update on REACH and the role of ECHA, together with the latest news from industry case studies. Supported by the Singapore Manufacturing Federation, this conference offers a unique opportunity to stay in line with international chemicals regulation and expectations of chemicals risk management in products.
Location and time:
15 February 2017, Singapore
Marina Mandarin Hotel, 6 Raffles Boulevard, Marina Square, Singapore 039594
- Dr Keng-Meng Khoo, Head of Regulatory Asia, Lonza
- Ms Stefanie Koh, Scientific Officer from the Pollution Control Department, National Environment Agency
- Mr Douglas Foo, President, Singapore Manufacturing Federation
- Dr Peter Di Marco, President, Australasian College of Toxicology and Risk Assessment (ACTRA)
- Ms Hui Foong Mei, Director – CHPB, Complementary Health Products Branch, Pre-Marketing Division, Health Sciences Authority, Singapore
- Mr Chalermsak Karnchanawarin, Managing Director of HazChem Logistics Management Co. Ltd. Thailand
- Ms. Yunjin Jean Cho, Assistant Manager, New Chemical Assessment and Regulatory Affairs, Chemtopia Co. Ltd, South Korea
- Remi Lefevre, Scientific Officer, ECHA, Finland
- Mr Darwin Lai, Regulatory Affairs Manager Asia Pacific, DSM Singapore Industrial Pte Ltd
- John Frangos, Associate, Principal Toxicologist, Golder Associates Pty Ltd, Australia
- Dr Kenkichi Fujii, Senior Risk Assessor, R&D - Safety Science, Kao Corporation, Japan
- Dr Seok Kwon, Procter & Gamble, Singapore
- Mike Freemantle, Head of Regulations, Lonza, Singapore
- Laura Robinson, Toxicology Consulting Ltd, UK
- Dr Salmaan H Inayat-Hussain, Head Global Toxicology Group Health, Safety and Environment (GHSE), Petronas, Malaysia
- Dr Jeremy Wong, Product Safety and Toxicology, The Estée Lauder Companies, Inc., USA
- Tina Qu, Regulatory Affairs Manager, Vshine
Full programme outline:
08.30 Registration & networking
Mr Douglas Foo
President, Singapore Manufacturing Federation
09.15 Keynote address: Risk based management of chemical hazards. What’s it all about?
- History of Human Health Risk Assessment (HHRA - environmental and occupational)
- Improving RA methods relating to environmental health
- Chemical Regulation in Australia: history and current overview
Dr Peter Di Marco
President, Australasian College of Toxicology and Risk Assessment (ACTRA)
Session 1: Country updates
Chair: Dr Keng-Meng Khoo
Head of Regulatory Asia, Lonza
09.40 Overview of NEA’s Hazardous Substances Management in Singapore
Ms Stefanie Koh
Scientific Officer from the Pollution Control Department, National Environment Agency
10.00 Guiding Principles for Complementary Health Products (CHP) Safety Assessment
Ms Hui Foong Mei
Director – CHPB, Complementary Health Products Branch, Pre-Marketing Division, Health Sciences Authority, Singapore
10.20 Regulatory Framework on Chemical Management in Thailand
In Thailand, the Department of Industrial Works (DIW), the competent authority (CA) for industrial chemicals, has initiated the regulatory framework on chemical management which aims at enhancing the current control through the Hazardous Substances Act (HSA) to become more risk based approach (REACH like system). This session will mainly focus on the current and future plan of DIW in progressing such changes in the coming years towards the achievement of SAICM goals in 2020.
Mr Chalermsak Karnchanawarin
Managing Director of HazChem Logistics Management Co. Ltd, Thailand
10.40 K-REACH and the new biocide regulation: update on progress and the methods that may be used for biocide risk assessment under the new system
- Update on K-REACH and product management including biocide
- Risk assessment for K-REACH; CSA procedure and CSR format, use descriptor, SIMPLE BOX for environmental emission
- Risk assessment for highly risk concerned product and Safety standard & Labelling
Ms. Yunjin Jean Cho
Assistant Manager, New Chemical Assessment and Regulatory Affairs, Chemtopia Co. Ltd, South Korea
11.15 Coffee break
11.35 REACH: contribution to a safer use of articles
- Main principles of REACH
- What the tools REACH contains serve the objective of safer use of articles and how these have been implemented (with what results) so far
- What areas of improvement or further developments can be envisaged for the future
Scientific Officer, ECHA, Finland
11.55 Risk Assessment methods used by authorities in Australia (NICNAS, APVMA, TGA) and how these assessments are tied to the registration process
Australian risk assessment practice is dependent on the type of chemicals. Overall the techniques are consistent with international guidelines. Industrial and agricultural chemical assessment methodologies have relied on the International Programme for Chemical Safety and for medicines the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). Recent focus for regulators has been how to balance regulatory effort based on risk. Besides a description of toxicology and risk assessment approaches in regulatory risk assessments in Australia. The presentation will consider the rapid assessment of existing chemicals by NICNAS and recent developments in APVMA risk assessment.
Associate, Principal Toxicologist,
Golder Associates Pty Ltd, Australia
12.15 Risk assessment and Regulatory Science updates in Japan
- The framework of the Japanese Regulation and them Regulatory Science
- Risk assessment for Japanese Cosmetics and quasi drugs, Chemical raw materials, Food/ Fictional food, Consumer products
Dr Kenkichi Fujii
Senior Risk Assessor, R&D - Safety Science, Kao Corporation, Japan
12.50 Lunch & Networking
Session 2: Industry Specific
13.50 ASEAN Guiding Principles on Safety Substantiation of Health Supplements. A case study - safety substantiation of a new active ingredient
Mr Darwin Lai
Regulatory Affairs Manager Asia Pacific, DSM Singapore Industrial Pte Ltd
14.10 The USA Risk Assessment landscape: industry expert
Dr Jeremy Wong
Product Safety and Toxicology, The Estée Lauder Companies, Inc., USA
14.30 Global non-animal-testing policy for cosmetics, chemicals and pesticides
Decades of investment in novel testing approaches to replace, reduce or refine animal use in toxicology have yielded a diverse toolbox
of validated in vitro methods, non-testing and other innovative strategies that could be put to immediate use across a number
of product sectors. Case studies from the pesticide and chemicals sectors will be used to examine progress and ongoing efforts toward uptake of available 3R approaches in key markets in the context of current international best practice and the ultimate goal of 21st century non-animal toxicology articulated by the U.S. National Research Council.
Regulatory Affairs Manager, Vshine
15.05 Coffee break
Session 3: Risk Assessment Case Studies
Chair: Mr Albert Khoo
Business Development and Regulatory Affairs Manager, 3M Technologies (S) Pte Ltd
15.25 Industry expert: case study
Dr Seok Kwon
Procter & Gamble, Singapore
15.45 Environmental Risk Assessment
Head of Regulations, Lonza, Singapore
16.05 Human Health Risk Assessment
Toxicology Consulting Ltd, UK
16.25 WHO Human Health Risk Assessment Toolkit: Towards Improved Chemical Risk Assessment.
The World Health Organization (WHO) Human Health Risk Assessment Toolkit was developed to aid decision making on potential risks of chemicals exposure. It demonstrates how to identify and acquire information needed to assess chemical hazards, exposures and risks and utilize the information to estimate potential exposure to hazardous chemicals and the corresponding health risks. Developed to assist professionals who are responsible for conducting health risk assessments and making decisions on risk management.
Dr Salmaan H Inayat-Hussain
Head Global Toxicology Group Health, Safety and Environment (GHSE), Petronas, Malaysia
17.00 Close of conference
Pre-conference Training Course: TOXICOLOGY & GHS/CLP
14 February 2017, 12.00-17.00
This short training course will provide an overview of the substance and mixture classification approach for human health effects in accordance with GHS/CLP and will cover the differences (where they arise) between these approaches.
It is designed to be a “hands on” course where attendees will have the opportunity to put their learning into practice by means of set examples. This will help re-enforce their learning and build their confidence in classifying and labelling both substances and mixtures.
The course will cover the following:
- Introduction to GHS/CLP and why classification is important
- Data sources and reliability
- Harmonised classification Vs Self-classification.
- Steps for classification of a substance and mixture
- Hazard classes (human health effects) and categories (health effects) including:
- Acute toxicity
- Skin corrosion/irritation
- Serious eye damage/eye irritation
- Respiratory or skin sensitisation
- Germ cell mutagenicity
- Reproductive toxicity
- Specific Target Organ Toxicity – Single Exposure (STOT-SE)
- Specific Target Organ Toxicity – Repeated Exposure (STOT-RE)
- Aspiration hazard
Throughout the training course worked examples will be used to illustrate the classification process and re-enforce the learning. Furthermore, the course manual will contain practice questions (with answers) for completion at the end of the course. Full lecture notes (in the form of a training manual) are included together with a copy of the presentation slides and homework.
is a qualified toxicologist and chemist with over ten years' experience in health, safety and environmental issues, as well as chemical compliance. Laura is an accomplished toxicology trainer, consultant and author of two published books on toxicology.
Post-conference: Practical Risk Assessment Training
16 February 2017, 08.45-16.30
This course has been arranged by Chemical Watch and offers a practical introduction to regulatory safety and risk assessment. It is intended for those with either little or no knowledge of the risk assessment process.
The course offers a comprehensive coverage of the basics of risk assessment, including what it achieves and the requirements under various country-specific regulations.
Furthermore, case studies and the opportunity to put the learning into practice will be a key feature of this course.
The learning outcomes are to allow those attending to understand the key data endpoints that make up risk assessment, covering toxicity, chemistry and exposure
- Background and Introduction
- Hazard identification and assessment
- Human health data gathering
- How to find and evaluate data for risk assessment purposes
- The use of chemistry knowledge (i.e. structure and physicochemical properties)
- Identification of critical studies for use in the derivation of benchmark “safe dose”
- Worked (and group) examples throughout this section
- Exposure assessment
- The approach which should be taken in exposure assessment and the type of models which can be used (why and how)
- The importance of chemistry in the assessment of likely exposure routes
- Worked (and group) examples
- Risk characterisation
- Risk perception
- Tolerable and acceptable risk
- Risk management
- Risk characterisation
- Case study
During this intensive training course, selected expert speakers will take participants through the concepts of risk, using practical case studies wherever possible. The day is intended for those who have basic knowledge of Risk Assessment.
is a qualified toxicologist and chemist with over ten years’ experience in health, safety and environmental issues, as well as chemical compliance. Laura is an accomplished toxicology trainer, consultant and author of two published books on toxicology.
Peter Di Marco
is a Fellow of the Academy of Toxicological Sciences (FATS; US), President, ACTRA and President Elect, IUTOX. Peter is regulatory toxicologist with over 35 years experience in research, teaching and risk assessment.
Dr Jeremy Wong
Product Safety and Toxicology, The Estée Lauder Companies, Inc., USA
Full price - USD$750
Chemical Watch Subscribers - USD$700
Members of Singapore Manufacturing Federation - USD$700
Pre-conference Training Course: Toxicology & GHS/CLP - USD$300
Post-conference Practical Risk Assessment Training - USD$500
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