Wednesday 10th May 2017
Safeware Quasar Workshop (2.30pm – 5pm)
Safeware Quasar invites customers attending SafeCom to attend a free workshop, designed to provide an insight into new software developments as well as additional regulatory updates not covered in the conference agenda. Register your interest in attending by emailing email@example.com.
Wednesday 10th May 2017
Evening Dinner and Networking Event
The conference will be launched with an informal dinner (for those who wish to attend), providing a superb opportunity for delegates to network with peers, stakeholders and industry experts. Delegates can register from 7pm until 7.50pm.
|Morning Session 1|
|8.30am – 9am||Registration (day delegates only)|
|9am – 9.10am||Simon Robinson
|Welcome and Morning Session Introduction|
|9.10am – 9.40am||Robin Foster
More about Robin
|Important Updates on EU-CLP Regulations and UN GHS developments
Robin will provide delegates with an update on CLP (10th, 11th and 12th ATPs), as well as the changes introduced in the 7th edition of the GHS.
|9.40am –10.10am||Andreas Herdina
More about Andreas
Helpnet is a network made up of ECHA and national helpdesks to improve cooperation on areas of common interest, thus providing a consistent and harmonised approach across all Member States. This is a positive new initiative from ECHA and goes a long way to helping SME’s improve their levels of compliance. How does ECHA see this developing to further assist SME’s? Andreas Herdina will provide an update.
|10.10am – 10.40am||Stacie Abraham
|U.S. TSCA Reform: An Overview with Focus on Global and EU Impact
Stacie will provide delegates with an update on the TSCA Reform.
|10.40am – 10.55am||Q&A|
|10.55am – 11.20am||Break/Exhibition/Networking|
|Morning Session 2|
|11.20am – 11.50am||Jonai Hiroshi
Head of Japanese Delegation UNSCEGHS
More about Jonai
|An Insight into Japanese GHS, Experiences to Date and New Developments
It is 18 years since the UN issued its first revision of GHS. Many countries around the world have now completed local implementations of the GHS framework. The letter “H” represents harmonization but how successful has this process been?
Jonai will share Japan’s experience of GHS as it is implemented today, describing the framework implementing the regulations for chemical classification, chemical hazard labelling and provision of safety data sheets (SDSs).
Jonai will also discuss plans for Japan implementing future revisions of GHS and the impact of other regulations such as ISHL, PRTR and the Poisonous and Deleterious Substance Control Act on GHS.
|11.50am – 12.20pm||Dr Richard Elsmore
More about Richard
|The BPR: Current Status and Upcoming Deadlines
As more active substances are approved under the EU’s biocide legislation, the second phase of the legislation (product authorisation) is now impacting a significant number of biocidal products that contain these actives. Due to the phasing of active substance evaluations the first authorisations have been for products such as rodenticides, wood preservatives and insecticides, but we are now getting to the stage where a broader range of products including some disinfectants need to be approved. Many of these have traditionally only been lightly regulated in some member states such as the UK, so the impact on companies formulating this type of product is likely to be significant.
This presentation provides an update on the current situation with both active substance approvals and product authorisation deadlines and should be of interest to companies that formulate biocidal products or that use biocidal products including preservatives in their formulated product. The impact of the BPR on treated articles is discussed with particular reference to labelling requirements.
|12.20pm – 12.50pm||Chris Packham
More about Chris
|The Selection and Use of Gloves as Protection Against Chemical Hazards
The selection and use of gloves as protection against chemical hazards is more complex than many realise. Except for very minor hazards all such gloves should be category III with the manufacturer’s performance data provided in accordance with EN374-3. However, this standard test is only indicative of what was achieved during the prescribed test and does not indicate what will be achieved when gloves are actually used. Many factors affect how gloves will perform in practical use. This talk will explain some of these and suggest how to create an effective glove system.
|12.50pm – 1.05pm||Q&A|
|1.05pm – 2.30pm||Lunch/Exhibition/Networking|
|2.30pm – 2.40pm||Simon Robinson
|Afternoon Session Introduction|
|2.40pm – 3.10pm||Mark Selby
Denehurst Chemical Safety
More about Mark
|The Communication of Hazardous Substances in Articles (REACH Article 33)
Under REACH there is a requirement to identify the risks associated with the chemicals present in articles (ie objects defined by shape including toys, medical devices, food contact, etc.) and to communicate the risk to recipients and/or users (Article 33). Substances of Very High Concern are defined in the REACH text and if present in articles with a risk of exposure to users, then their presence must be communicated adequately and users must be given advice on safe handling and disposal. However, REACH does not mandate the supply of SDSs with articles and the CLP Regulation excludes articles from formal labelling requirements. So, how do we effectively communicate and when is such communication necessary? And what happens if the substance is Authorised or Restricted? This presentation seeks to confirm the requirements for communication of substances in Articles and controls needed if on Annex XIV or Annex XVII of REACH.
|3.10pm – 3.40pm||Caroline Raine
More about Caroline
|Poison Centres – The Past, Present and Future
Caroline Raine, National Chemical Emergency Centre (NCEC), will explore the current poison centre landscape and how this is affected by REACH and CLP, specifically the recent update to CLP, Annex VIII.
Caroline will provide an overview of the specific country requirements focus on the intricacies of registrations such as the varying data requirements and submission processes. Additionally, looking at how these numbers are accessed and whether they are mandatory.
|3.40pm -4.05pm||Dr Andy Holton
More about Andy
|Update of the Model Regulations and Any Specific Implications for ADR/IMDG/IATA
Andy will examine recent changes to the Model regulations and assess the subsequent impact for the various modes of transport.
|4.05pm – 4.30pm||Q&A|