Characterizing Chemical in Commerce: Using Data on High Production Volume (HPV) Chemicals December 12, 2006 L. Twerdok, Ph.D, DABT NPPTAC Member Report.

Slides:



Advertisements
Similar presentations
1 Consumer Exposure Assessment at the U.S. Environmental Protection Agency: A ccomplishments and Opportunities for Global Collaboration Thomas Brennan.
Advertisements

The Toxic Substances Control Act of 1976 Christopher Dang Mr. Bodas P.4.
Summary Slide Some Industry views on POP/PBT identification in Europe.
Canada/Australia Issues being faced in the regulation of nano-materials Deborah Willcocks – Department of Health and Ageing, Government of Australia Anne-Marie.
Challenges and opportunities for effective implementation of TSCA Joel A. Tickner, ScD School of Health and Environment, UMASS Lowell US EPA National Pollution.
1 High Production Volume (HPV) Challenge Program Diane Sheridan Chief, Existing Chemicals Branch, Chemical Control Division, Office of Pollution Prevention.
1 Globally Harmonized System of Classification and Labelling of Chemicals (GHS): U.S. Update.
1 High Production Volume (HPV) Challenge Program – Future Directions Jim Willis Director, Chemical Control Division, Office of Pollution Prevention and.
Environmental Indexes by Amit Joshi. Purpose Assess the potential risks posed by releases from industrial sources Conduct preliminary impact assessment.
Identifying HPV Chemicals of That May Pose a Risk to the Great Lakes Fishery Lynda Knobeloch & Henry Anderson Wisconsin Dept of Health & Family Services.
EPA Tier I Screening Process and
EDSP Validation Gary E.Timm Senior Technical Advisor Office of Science Coordination and Policy U.S. Environmental Protection Agency.
NSF/ANSI STANDARD 61 FRAMEWORK FOR RISK ASSESSMENTS For use by Toxicology Sub-committee only Please do not copy or distribute.
Chemical Screening Programs Ted Smith Dale Phenicie.
Ecological Risk Assessment Definition -Evaluates the likelihood that adverse ecological effects may occur or are occurring as a result of exposure to one.
US EPA’s Chemical Management Wendy Cleland-Hamnett, Acting Director Office of Pollution Prevention and Toxics.
1 Use of HPV Challenge Data and the EPI Suite TM Model E. Laurence Libelo Economics, Exposure, and Technology Division Office of Pollution Prevention and.
1 Discussion of the 2006 Inventory Update Reporting Data December 12, 2006 Nhan Nguyen U.S. EPA.
Sustainability: Innovation Through Creative Use of Existing Tools Ruth Hull Intrinsik Environmental Sciences Inc, Toronto, Canada SETAC (Society of Environmental.
1 International/OECD Nanotechnology Activities EPA/DoD Meeting on Nanotechnology March 9, 2007 Jim Willis, EPA/OPPT.
Dr. Manfred Wentz Director, Hohenstein Institutes (USA) Head, Oeko-Tex Certification Body (USA) AAFA – Environmental Committee Meeting November 10, 2008.
1 International Harmonization Efforts on Petroleum Substances Characterizing Chemicals in Commerce: Using Data on High Production Volume (HPV) Chemicals.
United States Chemicals Management Petroleum Sector Approach Jennifer Galvin, PhD, DABT, CIH Sound Management of Chemicals Working Group – Stakeholder.
GHS CLASSIFICATION ONLINE. Registration: Click on “Register”
International Initiatives and the U.S. HPV Challenge Program Ken Geiser, PhD Lowell Center for Sustainable Production University of Massachusetts Lowell.
EDSP’s Approach to Test Protocol Validation Office of Science Coordination and Policy U.S. Environmental Protection Agency.
U.S. High Production Volume (HPV) Challenge Program Diane Sheridan U.S. Environmental Protection Agency October 25, 2005 Region 2 Emerging Chemicals Workshop.
“The Dose makes the Poison”
U.S. Food and Drug Administration Notice: Archived Document The content in this document is provided on the FDA’s website for reference purposes only.
Chad B. Sandusky, Ph.D. Physicians Committee for Responsible Medicine, Washington DC, USA STRATEGIES TO REDUCE ANIMAL TESTING IN US EPA’S HIGH PRODUCTION.
U.S. High Production Volume (HPV) Challenge Program Diane Sheridan U.S. EPA, Office of Pollution Prevention and Toxics December 12, 2006.
Volker J. Soballa, Evonik Industries AG Introduction and Overview of ICCA GPS Risk Assessment Guidance Copyright© 2012 ICCA All Rights Reserved Responsible.
1 Selected Current and Suggested Ideas on Uses of HPV Challenge Data Nhan Nguyen US EPA Characterizing Chemicals in Commerce: Using Data on High Production.
Forging Partnerships on Emerging Contaminants November 2, 2005 John Vandenberg Associate Director for Health National Center for Environmental Assessment.
Charge Question 4-1: Please comment on the ecotoxicity studies selected to represent the most sensitive species in each of the risk scenarios (acute aquatic,
Identifying Tools to Rapidly Characterize & Prioritize Chemicals in Commerce for Prevention Joel A. Tickner, ScD Lowell Center for Sustainable Production.
Phasing Out PFOS and PBDEs: Voluntary and Regulatory Steps Kenneth Moss Chemical Control Division Office of Pollution Prevention and Toxics, EPA HQ October.
Translating HPV Information into Plain Language Characterizing Chemicals in Commerce Austin, TX December, 12-14, 2006.
1 Chemical Assessment and Management Program Tala Henry, ChAMP Coordinator Office of Pollution Prevention and Toxics U.S. Environmental Protection Agency.
Advisory Committee Kickoff Meeting SWRCB Program to Develop Sediment Quality Objectives for Enclosed Bays and Estuaries of California July 29, 2003 CAL/EPA.
Malaysia Update on “draft” proposal for the Environmentally Hazardous Substance (“EHS”) Notification and Registration Scheme.
GPS Implementation: Examples and Challenges Dr. Ahmed Al-Hazmi Manager, Environmental Affairs 25 September 2012.
December 2006Characterizing Chemicals in Commerce 1 Using the EPA HPVIS to Form Chemical Categories for Hazard Assessment Sandra Reiss Murphy, PhD Arkema.
September 22, 2011 Office of Pollution Prevention and Toxics1.
Measurement and Targeting – Design and Implement Programs to Track Results and Accountability National Environmental Partnership Summit 2006 Wednesday,
CALIFORNIA’S AIR TOXICS PROGRAM: IMPROVEMENTS TO ASSESS HEALTH RISK Update to the Air Resources Board July 24, 2014 California Environmental Protection.
Design for the Environment Program Characterizing Chemicals in Commerce Austin, Texas December 13, 2006 Clive Davies U.S. Environmental Protection Agency.
1 Nanoscale Materials Stewardship Program Environmental Summit May 20, 2008 Jim Alwood Chemical Control Division Office of Pollution Prevention and Toxics.
Environmental Protection Agency 1 The High Production Volume Information System (HPVIS) Demonstration and Status National Environmental Partnership Summit.
A Global Review of Methodologies for Aquatic Ecological Risk Assessment.
Prioritization Process and Development of the Hazard Characterization Documents Office of Pollution Prevention and Toxics U.S. Environmental Protection.
Criteria for Inherently toxic (iT) in CEPA, UNEP Proposed iT criteria for non-human organisms –aquatic acute effects levels of < 1 mg/L –above 1 mg/L.
Characterizing Chemicals in Commerce: Reflections and Wrap-Up Steven Russell American Chemistry Council December 14, 2006.
California Sediment Quality Advisory Committee Meeting SWRCB Program to Develop Sediment Quality Objectives for Enclosed Bays and Estuaries of California.
1 State of Play Prioritisation of Substances By modelling Hazard & Exposure Klaus Daginnus Institute for Health & Consumer Protection Joint Research Centre,
Office of Pollution Prevention and Toxics Development of the High Production Volume Information System (HPVIS) December 12, 2006 Characterizing Chemicals.
The new chemicals risk matrices. Workshop focus use of new online categorisation tools criteria used to categorise new chemicals under the proposed framework.
Abstract A step-wise or ‘tiered’ approach has been used as a rational procedure to conduct environmental risk assessments in many disciplines. The Technical.
Overview of the CPSC Directorate for Health Sciences * Mary Ann Danello, Ph.D. Associate Executive Director * The views expressed in this presentation.
Classification. Hazard Classification The GHS is designed to identify and classify the “hazards” of the substances or mixtures, and to communicate those.
Use of Borates in Swimming Pools: Consideration of Health Effects
ICCA GPS Risk Assessment and Guidance
Endocrine Disruptor Screening and Testing: An Industry Update
Communication: Safety Summary
GC Chemical Characteristics Task Group
OECD work on manufactured nanomaterials
Categorization of the Canadian Domestic Substances List
International Initiatives and the U.S. HPV Challenge Program
ATSDR Office Of Tribal Affairs
VICH GL 54, Studies to evaluate the safety of residues of veterinary drugs in human food: General approach to establish an Acute Reference Dose (ARfD)
Presentation transcript:

Characterizing Chemical in Commerce: Using Data on High Production Volume (HPV) Chemicals December 12, 2006 L. Twerdok, Ph.D, DABT NPPTAC Member Report on the National Pollution Prevention and Toxics Advisory Committee (NPPTAC): The HPV Data Screening Process

2 HPV Data Screening Process NPPTAC Mission & Background Present the screening process and screening criteria Present process validation results screening 53 HPV chemicals Purpose of Presentation

3 HPV Data Screening Process Provide advice & recommendations on overall policy and operations of EPA OPPT Risk Management: HPV, VCCEP, RTK programs Risk Communication: public RTK Pollution Prevention: PBTs, Green Chemistry, DfE Coordination of TSCA & P2 among EPA; Federal, State, Tribal, local gov’ts; NGO NPPTAC Mission

4 HPV Data Screening Process NPPTAC formed under the Federal Advisory Committee Act Chartered September, 2002 Multi-stakeholder representation Academia/research Industry Non-governmental organizations States Tribes OPPT & Federal Technical Advisors NPPTAC Background

5 HPV Data Screening Process Issue Data submissions on ~1,400 chemicals in U.S. HPV Challenge Program Requirements Management tool to logically arrange review order of HPV submissions Establish a review process for determining hazard potential based on data in HPV submissions Conservative screening process Screening Process Goals

6 Categories: OPPT Evaluates Category Analysis HPV Data Screening Process Flow Single Chemicals or Complex Class 2 Category EPA Risk Characterization Activities, such as: Human or Eco. Exposure Characterization Further Hazard Characterization Under Review Elsewhere? Refer to other EPA Office, Agency, etc. Others Voluntary / Regulatory Action to Collect / Share Information Vol. / Reg. Action to Manage Risk No Further Action Based on Findings New Information (e.g. IURA Data) No Further Hazard Characterization Required at This Time Additional Hazard Information Tier 1: Sort for Order of OPPT Review (Automated Process) First ThirdSecond Tier 2: Screening-Level Hazard Characterization HPV TIER PROCESS OPPT Disagrees OPPT Agrees Automated/ Manual Sort into Review Group 1, 2, or 3

7 HPV Data Screening Process Screening uses a subset of HPV required health and environmental hazard endpoints (SIDS*)  common starting point  partially automated process Utilize much of OECD ’ s GHS** criteria Tested with actual HPV data Tier I Screening Criteria: Overview * Screening Information Data Set ** Globally Harmonized System for Classification & Labeling of Hazardous Substances

8 HPV Data Screening Process Chemicals sorted into first, second, or third group for OPPT review Chemicals assigned preliminary review group based on: human health effects data environmental effects data Highest preliminary review group is assigned as the final review group Now, walk through criteria Tier I Screening Criteria: Application

9 HPV Data Screening Process Primary endpoint  Repeat Dose Toxicity Repeat dose results modified by Genetic toxicity (gene and chromosome) Reproductive toxicity Developmental toxicity Positive results for any one will move up one or more review groups, e.g. Third  Second Third  First Health Effects

10 HPV Data Screening Process ROUTE OF EXPOSUREUNITS First GroupSecond Group Oral (rat)mg / kg body weight/ day  Dermal(rat or rabbit)mg / kg body weight/ day  Inhalation (rat) gasppm / 6h / day  Inhalation (rat) vapourmg / litre / 6h /day  Inhalation (rat) dust/mist/fumemg / litre / 6h / day   Criteria applied to LOAEL (if only NOAEL provided, use NOAEL)  Chemicals that do not meet first or second group criteria  third  Criteria above for 90-day studies (tripled for 28-day studies) Health Effects Primary Endpoint  Repeat Dose Toxicity LOAEL = Lowest Observed Adverse Effect Level NOAEL = No Observed Adverse Effect Level

11 HPV Data Screening Process Primary Endpoints  Toxicity to fish, aquatic invertebrate (Daphnia), and algae Rank based on GHS criteria for LC 50 or EC 50 : First group< 1 mg/L Second group1 – 10 mg/L Third group> 10 mg/L Final environmental group = highest received among the three endpoints At OPPT’s discretion, environmental fate may further modify ranking Log K ow (octanol/water partition coefficient) Biodegradation Environmental Effects LC 50 or EC 50  median lethal (L) concentration or effective (E) concentration for 50% of the test population

12 HPV Data Screening Process Examples of Using Screening Criteria Human Health Ecotox Exceeds Env. Fate Criteria? FINAL Submission No. Repeat Dose Final Health Effects 82 nd 1 st No1 st 103 rd Both1 st or 2 nd 183 rd No3 rd 392 nd 3 rd Fail Biodeg.1 st 3053 rd 2 nd No2 nd

13 HPV Data Screening Process First Group29 (55%) Second Group 9 (17%) First or Second Group 4 ( 8%) Third Group 6 (11%) Unable to Classify* 5 ( 9%) Validation Based on 53 HPV Submissions *Unable to Classify because testing has been proposed, data are missing, or EPA and sponsor disagree about data

14 EPA critically evaluates data in HPV Challenge Program submissions Evaluate data quality and completeness Data not accepted at face value as in automated Tier I screening process Develop a screening-level hazard [not risk] assessment based on data provided by the sponsors Hazard assessments are culmination of Challenge Program Inform sponsors and public of EPA findings HPV Data Screening Process Tier II: Purpose

15 Tier II screening level hazard characterizations will then lead back into normal OPPT chemical management activities Chemical/category has low hazard potential; no further action required at this time new information in future could warrant reevaluation Chemical/category hazard potential is identified; OPPT options: Identify existing voluntary/regulatory risk management programs and practices to determine adequacy Require information gathering – hazard and/or exposure Initiate EPA-lead risk assessment Refer to more appropriate federal program for assessment Decide after closer examination that no further action is needed at this time HPV Data Screening Process Post-Tier II Activities

16 Categories: OPPT Evaluates Category Analysis HPV Data Screening Process Flow Single Chemicals or Complex Class 2 Category EPA Risk Characterization Activities, such as: Human or Eco. Exposure Characterization Further Hazard Characterization Under Review Elsewhere? Refer to other EPA Office, Agency, etc. Others Voluntary / Regulatory Action to Collect / Share Information Vol. / Reg. Action to Manage Risk No Further Action Based on Findings New Information (e.g. IURA Data) No Further Hazard Characterization Required at This Time Additional Hazard Information Tier 1: Sort for Order of OPPT Review (Automated Process) First ThirdSecond Tier 2: Screening-Level Hazard Characterization HPV TIER PROCESS OPPT Disagrees OPPT Agrees Manual Sort into Tier Group 1, 2, or 3

17 Questions? For more information: ommendationfeb2005.pdf (complete NPPTAC screening recommendation) ommendationfeb2005.pdf Lorraine Twerdok: