Beruflich Dokumente
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2015 MANAGEMENT
SYSTEM GUIDANCE
MANUAL JOINT ROADMAP
DELIVERABLE
ZERO DISCHARGE
OF HAZARDOUS
CHEMICALS PROGRAMME
I N A S S O C I AT I O N W I T H
ES121114083500GNV
Contents
Section Page
Acronyms and Abbreviations........................................................................................................ v
Introduction ..................................................................................................................... INTRO-1
Overview......................................................................................................................... INTRO-1
ZDHC Goal....................................................................................................................... INTRO-1
Objective ........................................................................................................................ INTRO-1
ZDHC CMS Goals ............................................................................................................. INTRO-2
Engagement with ZDHC Stakeholders ............................................................................ INTRO-2
Structure of the CMS Manual ......................................................................................... INTRO-3
1 Commitments to CMS ................................................................................................... 1-1
1.1 Management Statement ........................................................................................... 1-1
1.1.1 Requirements ............................................................................................... 1-1
1.2 Scope of CMS............................................................................................................. 1-1
1.2.1 Requirements ............................................................................................... 1-1
2 Assessment, Planning and Prioritisation ........................................................................ 2-1
2.1 Systematically Identify and Document Chemicals Used and Stored in Your
Organisation .............................................................................................................. 2-1
2.1.1 Purpose......................................................................................................... 2-1
2.1.2 Facility Plan and Walk Through .................................................................... 2-1
2.1.3 Chemical Material Flow Diagrams (Element 2.1.2) ...................................... 2-2
2.1.4 Creating a Comprehensive Chemical List ..................................................... 2-2
2.2 Regulatory Assessment ............................................................................................. 2-5
2.2.1 Monitoring Regulations and Permits ........................................................... 2-5
2.2.2 Verification of Compliance ........................................................................... 2-6
2.3 Procurement/Supplier Practices ............................................................................... 2-6
2.3.1 Chemical Purchasing Policy Considerations ................................................. 2-7
2.3.2 Identify Chemical suppliers .......................................................................... 2-8
2.3.3 Supplier Approval/Removal Process ............................................................ 2-9
2.4 Chemical Risk Assessment......................................................................................... 2-9
2.4.1 Hazard and Risk Assessment ........................................................................ 2-9
2.4.2 Environmental ............................................................................................ 2-10
2.4.3 Health and Safety ....................................................................................... 2-11
2.5 Chemicals and Processes of Concern ...................................................................... 2-12
2.5.1 Identify Gaps and Losses in Current Processes .......................................... 2-12
2.5.2 RSL and MRSL Process ................................................................................ 2-13
2.6 Performance Goals and Action Plans ...................................................................... 2-14
2.6.1 MRSL Compliant Formulations ................................................................... 2-14
2.6.2 Alternatives Assessment ............................................................................ 2-14
3 Chemicals Management ................................................................................................ 3-1
3.1 Organisational Structure ........................................................................................... 3-1
3.1.1 Roles and Responsibilities ............................................................................ 3-1
3.1.2 Communication ............................................................................................ 3-2
3.2 Training ...................................................................................................................... 3-2
3.2.1 Management ................................................................................................ 3-2
3.2.2 Regulatory .................................................................................................... 3-2
3.2.3 Work Practices.............................................................................................. 3-2
3.2.4 ZDHC Training ............................................................................................... 3-3
3.3 Document Development ........................................................................................... 3-3
Section Page
3.4 Document and Record Control.................................................................................. 3-3
3.5 Chemical Management Work Practices .................................................................... 3-4
3.5.1 Exposure Control Measures ......................................................................... 3-4
3.5.2 Safety Data Sheet Management .................................................................. 3-5
3.5.3 Chemical Handling ........................................................................................ 3-6
3.5.4 Chemical Storage.......................................................................................... 3-6
3.5.5 Chemical Transportation .............................................................................. 3-6
3.5.6 Chemical Labelling ........................................................................................ 3-7
3.5.7 Chemical Use – Regular and Optimisation ................................................... 3-7
3.5.8 Personal Protective Equipment.................................................................... 3-7
3.5.9 Laboratory Practices..................................................................................... 3-8
3.5.10 Maintenance and Housekeeping ................................................................. 3-8
3.5.11 Waste and Disposal ...................................................................................... 3-9
3.6 Emergency Procedures.............................................................................................. 3-9
4 Monitor ........................................................................................................................ 4-1
4.1 Monitor and Measurement (Continuous Improvement) .......................................... 4-1
4.1.1 Goal Progress................................................................................................ 4-1
4.1.2 Regulatory Compliance ................................................................................ 4-1
4.1.3 Work Practice and Customer Requirements Implementation..................... 4-1
4.2 Internal Audit ............................................................................................................ 4-2
4.3 External Audit ............................................................................................................ 4-2
4.4 Change Management and Corrective Action ............................................................ 4-2
4.4.1 Change Management ................................................................................... 4-2
4.4.2 Corrective Action .......................................................................................... 4-3
5 Management Review .................................................................................................... 5-1
5.1 Disclosure of Substance in Use.................................................................................. 5-1
5.2 Stakeholder Review ................................................................................................... 5-1
5.3 Management Review ................................................................................................ 5-2
6 CMS Resources ............................................................................................................. 6-1
7 Glossary........................................................................................................................ 7-1
Appendixes
A Assessing Status
B Tables
C Chemical Inventory
D Risk Assessment Template Example
E AAFA Environmental standards
Introduction
Overview
This Chemical Management System (CMS) Guidance Manual focuses on the approach, structure and
documentation needed to create and support a Zero Discharge of Hazardous Chemicals (ZDHC)
Programme CMS. Information provided in this manual should be easily internalised by retailers,
brands and their supply chain partners while accommodating the complexities of the ZDHC roadmap
work and the textile supply chain chemistry applications. This framework will build on ISO
management standards and other applicable frameworks, such as the Deutsche Gesellschaft für
Internationale Zusammenarbeit (GIZ) Practical Chemical Management Toolkit and the Outdoor
Industry Association (OIA) Chemicals Management Working Group (CMWG) Framework. A sound
chemical management system is paramount to worker safety and will reduce environmental impacts
on the community and the broader environment. A CMS is therefore one of the cornerstones for
ensuring continuous improvement towards our 2020 goal of zero discharge of hazardous chemicals
throughout the life cycle of our products.
A CMS provides the ZDHC Group, its suppliers and other stakeholders a well‐defined structure to
move toward zero discharge. A management system is a framework that allows inclusion of all
projects introduced in the Joint Roadmap, Version 2.
Specifically, the ZDHC Group affirms that:
• A CMS is an effective framework for improving overall environmental and chemical performance
while achieving the goal of zero discharge.
• A management approach allows continuous chemical management improvement and
minimisation of environmental impact.
• A management approach can provide the structure for current roadmap projects.
• A management approach allows an entry point for different actors in the supply chain, including
the chemical industry, brands, Tier 1 and 2 suppliers and other stakeholders who wish to
contribute to the success of the ZDHC Group’s commitment.
The CMS Guidance Manual is intended to be a living document that will be periodically updated. This
first version of this manual focuses mainly on foundational matter. Later versions will include more
detailed content on progressive and aspirational matters.
ZDHC Goal
The ZDHC Group’s goal is to achieve zero discharge of hazardous chemicals across supply chains and
product life cycles in the production of apparel, footwear and accessory goods by 2020. The group
has developed tools like the Manufacturing Restricted Substances List (MRSL) and chemical guidance
sheets to improve chemical management and to assist facilities in achieving or maintaining
compliance with retailer, brand and government regulations. These tools fit within the CMS
framework in this guidance manual.
Objective
The ZDHC CMS objective is to develop a management framework that assists brands, retailers, Tier 1
and 2 suppliers and chemical suppliers in understanding their roles, by developing clear guidelines
that allow all committed supply chain stakeholders to participate and take responsibility for their part
of the value chain. This level of alignment and harmonisation will be key to delivering on the ZDHC
vision, mission and 2020 goal. Documentation in this manual includes outcomes of the ZDHC Group’s
work activities and thereby creates a comprehensive, yet pragmatic management system.
By developing a CMS structure for the apparel and footwear supply chain that includes all our existing
and future work activities, we provide the ZDHC programme with a sound structure that is
recognised, understood and easy to communicate to the textile industry.
Commitments to CMS
The first step in implementing any chemical management system is for an organisation to clearly and
publicly commit to the system. Such commitments clearly indicate an organisation’s overarching
strategy and intentions.
The SDS is the first place to look for hazardous and risk exposure information. Using information from
any of the above sources, the facility should create a hazard and risk assessment inventory that includes:
1. Chemical names: From inventory created in CMS Element 2.1
a. Common
b. CAS number
2. Process: Production, final product, laboratory, maintenance, discharge and other relevant
information
3. Area: Examples include dye kitchen, storage and printing
4. Supplier: Emergency contact information
5. SDS: Availability of SDS, Yes or No
6. Hazard statement: R-phrases from the SDS
7. Hazard type: Physical (flammability, explosivity), health (carcinogenicity, toxic to reproduction)
and environmental (bioaccumulative, persistency, eco-toxicity)
8. RSL/MRSL: Compliant chemical, yes or no
9. Amount per usage/batch/process: Estimate of how much of the chemical is used at one time
10. Amount lost to the environment: Use of information developed from mass balance and waste
records; estimate of the quantities of chemicals lost to the environment
11. Hazard Prioritisation: Prioritisation and ranking of the overall risks of the chemicals. See
Appendix D for Risk Assessment Template example
All work areas must at all times maintain an inventory of the hazardous chemicals according to the
following guidelines:
• When new hazardous chemicals are acquired, they must promptly be added to the inventory.
• When hazardous chemicals are expended or disposed, they must be removed from the inventory
or a single line shall be drawn through them.
• The inventory must be examined and updated periodically (at least annually).
• The inventory must be readily available to anyone entering the work area.
Safe Work Australia maintains a document on their web site called Managing Risks of Hazardous
Chemicals in the Workplace Code of Practice. This document includes good reference materials.
Appendix F (Overview of a Risk Assessment Process) and Appendix G (Risk Assessment Checklist) at
this web site also are useful hazard and risk management tools.
ZDHC Audit Questions
2.4.2 Environmental
Has the organisation established procedures
Expected CMS Deliverable: Process/Plan for to ensure that all wastes are collected and
Reducing Environmental Impacts handled in a timely and environmentally
Establish, document and implement a process for responsible manner and in accordance with
identifying and controlling the potential environmental any applicable legal/regulatory
impacts from use of their chemical inventory. For each requirements? (CMD 2.1.14)
of the below areas, the organisation should identify Do maintenance shops, laboratory and
environmental roles and responsibilities, where wastes other ancillary spaces practice proper
or discharges occur, appropriate control mechanisms chemical waste disposal? (CMW 2.1.12)
for discharges and how to monitor the control
mechanisms. The organisation also should set goals to reduce chemical wastes or discharges.
Environmental media that could be impacted are:
• Air • Noise and nuisance
• Soil • Waste and sludge
• Groundwater • Wastewater
An organisation also should establish, document and implement a process for monitoring and setting
goals to reduce their environmental impact. See Appendix E for example environmental standards
from the American Apparel and Footwear Association (AAFA).
A Job Safety Analysis (JSA) is one of the risk assessment tools used to identify and control workplace
hazards. The aim of a JSA is prevention of personal injury to a person or their colleagues and
workplace. A JSA is also known as an Activity Hazard Analysis (AHA), Job Hazard Analysis (JHA) and
Task Hazard Analysis (THA).
The JSA should be created by the work group performing the task. If available, it can be expedient to
review a prepared JSA that has been performed before. When conducting this type of JSA, the work
group must review all of the steps thoroughly to ensure that they are controlling all of the hazards for
this job. A JSA is usually completed on a form with the most common configuration a three column
table (although many companies include additional columns). Typical three column headings include:
1. Job step
2. Hazard
3. Controls
A hazard is any factor that can cause damage to personnel, property or the environment. Some
companies include loss of production or downtime in the definition as well. A control is any process in
place for controlling a hazard.
The work group should initially breakdown the task into its component steps and then identify
hazards for each step. Controls should be recorded in column three of the JSA for each hazard
identified.
Create (and maintain a chemical inventory list which references MRSL compliant formulations and
their suppliers and update this list annually. Set an annual chemical inventory goal for the percentage
of formulations that are MRSL compliant and work towards that goal through the development of
action plans, assigned responsibilities, timeframes for actions and an estimate of resource needs
(e.g., financial, human). This list of substances should represent chemicals that score well on the
hazard and risk assessment inventory (CMS Element 2.4.1) and that have low to near zero discharges
to the environment. The ZDHC Group has set a high priority for eliminating or substituting hazardous
chemicals in our members’ products and their manufacture by 2020.
Develop a process to phase out the intentional use of ZDHC Audit Questions
priority hazardous chemicals using clear target dates. Does the facility have programmes in place
A chemical inventory with a hazard assessment and to phase out the intentional use of the 11
MRSL compliant formulations is a great starting point priority chemical groups, as defined by the
for review and goal setting. Discussions and action plans ZDHC Group, with clear target dates?
should be formed with the chemical supplier to ensure (CRC 1.1.2)
a successful target completion date without impacting
the facility’s process efficiency and product performance.
For guidance on the industry’s best management practices, regarding chemical management, see
additional CMS Resources in Section 6.
2.6.2 Alternatives Assessment
Expected CMS Deliverable: Best Practice Alternative Assessment
Establish, document and implement a process for assessing alternatives for chemicals that are found
to have significant hazards, risks or discharges and set an annual goal for the number of alternatives it
will assess. The process for assessing alternatives should include the development of action plans,
assigned responsibilities, timeframes for actions and an estimate of resource needs (e.g., financial,
human) to conduct the assessment.
Chemicals Management
Responsible for RSL and MRSL compliance and communication with supply chain
RSL and MRSL Oversight
partners
Community of Practice and Acts as organisation’s representative for Chemical Management Community of Practice
Sustainable Chemistry Responsible for chemicals management and sustainable chemistry metrics
3.1.2 Communication
Expected CMS Deliverable: Safety Communication/ ZDHC Audit Questions
Hazardous Chemical Placards/Posted PPE Does the facility have a current (chemical)
Warnings SDS for each chemical, provided in the local
language and placed in chemical handling
Establish, document and implement a process for
and storage areas? (CMW 2.1.2)
communicating about the CMS amongst all of levels of
the organisation. An organisation also should establish, Has management established procedures
document and implement a process for receiving and that clearly define and communicate the
areas in which authorised personnel are
responding to external stakeholders, including
allowed to enter? (Primary focus is
documenting communications.
chemicals.) (CMW 2.1.5)
3.2 Training Is there a chemical emergency response
plan in place and practiced on a planned
To achieve a goal of zero discharge of hazardous schedule? (CME 2.1.1)
chemicals, organisations should:
1. Ensure that personnel are competent through appropriate education, training or experience.
Train employees about:
a. Preventive environmental and work safety practices
b. Saving resources
c. Proper use of goggles and face shields to avoid eye and skin contact
d. Use of protective clothing to avoid skin contact with chemicals
e. Selecting suitable gloves and removing gloves to avoid skin contact with chemicals
f. Proper hand washing
2. Retain associated chemical records ZDHC Audit Questions
3. Establish, document and implement a process to Are training records maintained to
conduct and track training demonstrate that facility personnel handling
chemicals have the required education,
4. Assess training effectiveness with a quiz or by training and skills to perform their assigned
monitoring an appropriate activity to demonstrate responsibilities and activities? (CMT 2.1.1)
learning
5. Ensure that personnel are aware of the relevance and importance of their activities and how they
contribute to achieving chemical objectives
3.2.1 Management
Establish, document and implement a process for informing top management of their roles in
managing chemicals. Include information about the hazards and risks associated with the existing
chemical inventory, the improvement goals of the organisation and the human and financial resource
needs for CMS implementation.
3.2.2 Regulatory
Establish, document and implement a training process for making appropriate staff knowledgeable
about the legal requirements (CMS Element 2.2) associated with chemicals in the organisation’s
inventory (CMS Element 2.1.3).
3.2.3 Work Practices
Establish, document and implement a process for making chemical-handling staff aware of
appropriate work practices. At a minimum, appropriate staff should be trained on the SOPs created
to fulfil CMS Element 3.5.
Keep SDS up to date and review regularly for new Has the organisation established and
implemented procedures to ensure
content (at least annually).
chemicals used are from oldest to newest
• Do not mix unknown chemicals. receipt date? (CMD 2.1.12)
• Do not use food containers for chemicals and do not eat near chemicals.
• Use ventilation systems to reduce chemical inhalation of dust/fumes.
• Do not smoke near chemical storage areas.
• Wash hands after handling chemicals.
ZDHC Audit Questions
3.5.8 Personal Protective Equipment
Is there an internal audit group that reviews,
CMS Deliverable: Procedure for PPE Use audits and verifies chemical hazards and
The main purpose of PPE should be to protect inventory? (CAA 3.1.1)
employees should an accident or incident occur despite Is there adequate space in and around
appropriate management systems and operational weigh areas, machinery and storage along
procedures. with appropriate environmental controls to
preclude mix ups or contamination?
Information on appropriate PPE can be found in the SDS (CMW 2.1.8)
for each chemical. PPE includes the following:
Have boiler and effluent treatment
• Eyes: Wear appropriate protective eyeglasses or chemicals been inventoried and
chemical safety goggles as described by the U.S. categorized? (CMW 2.1.15)
Occupational Safety and Health Administration’s
(OSHA’s) eye and face protection regulations in 29CFR 1910.133 or European Standard EN166.
6/5/08 Aluminium 7429-90-5 100% N/A 500 g Glass 200 g Chemical Storage
MA Room 110
Monitor
─ Continually improve the effectiveness of the Is there a corrective action plan in place for
the facility non-compliance? (CRR 1.1.2a)
CMS
Is there a documented procedure to deal
• Include determination of applicable methods, with chemical spills and leaks? (CMD 1.1.13)
including statistical techniques, and the extent of
their use in the plan. Does the facility maintain appropriate spill
containment kits in use and storage areas?
4.1.1 Goal Progress (CMW 2.1.13)
Establish, document and implement a process to Is there a chemical emergency response
monitor progress towards the goals created in CMS plan in place and practiced on a regular
Element 2.6. Make sure to document information used schedule? (CME 2.1.1)
to monitor performance and maintain associated Is management aware of the ZDHC 11
records. priority chemical groups and ZDHC goal of
4.1.2 Regulatory Compliance zero discharge? (CAG 3.1.1)
Does the facility have targets in place to
CMS Deliverable: Process to Monitor Regulatory
reduce or eliminate the use of hazardous
Conditions
chemicals in the facility? (CAG 3.2.1)
Establish, document and implement a process to
Does the facility set and review, at least
monitor progress towards regulatory conditions annually, formal targets to reduce the
identified in CMS Element 2.2. These could include amount of hazardous substances used?
MRSL, RSL, wastewater discharge limits, air emission (CAG 3.2.2)
restrictions or other qualitative or quantitative
conditions set through regulation or permits. Make sure to document performance and maintain
associated records. Equipment needed to conduct the measurements should be calibrated and
associated records maintained as well.
Management Review
5.1 Disclosure of Substance in Use
CMS Deliverable: Process for Disclosing
Substances in Use ZDHC Audit Questions
Does the facility have chemical hazard
Establish, document and implement a process for signage and safe handling equipment
disclosing the substances in use. An organisation should available in areas of the facility where
determine and document which stakeholders will be exposure could occur? (CD 4.1.1)
provided the substance in use information and how the
Is the annual usage (volume) of each
information will be communicated. The chemical risk
chemical monitored and recorded?
assessment information gathered in Section 2.4 can (CRS 1.1.4)
provide the basis for an organisation’s disclosure
practices.
4. Regulatory changes
5. Input from stakeholders
6. Follow-up actions from previous management reviews
7. Changes that could affect the CMS
8. Recommendations for improvement
Senior management should be responsible for providing feedback on how to improve the system and
guide the organisation closer to the goal of zero discharge of hazardous chemicals.
Documents and records, including meeting minutes, indicating performance of this element shall be
maintained.
CMS Resources
Organisational Skill CMS Manual Section Title & Description Hyperlink
Level (Symbol) Reference
Foundational
Progressive
Aspirational
Glossary
alignment agreement
analytics lab reports from air, soil and water chemical testing
audit an inspection or review
best practices processes and procedures exceeding requirements to achieve
best results
brand a trademark or distinctive name identifying a product, service
or organisation
downstream pertains to the latter part of a process or system
framework organisational structure used to manage or create
key performance indicator unit of measure to mark whether or not wanted progress is
being made
law/regulation statements from states and countries requiring adherence to
specific standards and protocols
life cycle from initial creation to final disposition
Manufacturing Restricted Substances list of substances banned from intentional use in processing
List (MRSL)
metrics type of measurement used to gauge some
measurable/quantifiable component of performance
milestone critical project/deliverable/performance date or
accomplishment
prioritisation determining level of importance relative to others
Restricted Substances List (RSL) information related to regulations and laws that restrict or ban
certain chemicals and substances in finished home textile,
apparel and footwear products around the world
retailer the business which sells goods or commodities directly to
consumers
stakeholder individual or organisation with an interest in the outcome or
status
supply chain system of activities, information and resources involved in
moving a product or service from supplier to customer
tier 1 suppliers tier 1 suppliers sell their product directly to major brands
tier 2 suppliers tier 2 suppliers sell their product to a company that then sells
product directly to the major corporation
training providing knowledge to improve competency and overall
capabilities
zero discharge of hazardous chemicals non-detectable limit based on best available testing capability
ZDHC MRSL compliance formulations list of chemicals/chemical formulas that comply with the
facility’s MRSL/RSL
Does your facility have written statements from the senior level
leadership of your company clearly communicating the
organisation’s goals and aspirations around Corporate Social
Responsibility?
Are you able to verify that your facility only utilises chemicals that
are in compliance with:
a. Regulations where your products are manufactured and sold?
b. Your customer’s MRSL/RSL?
c. Contract obligations?
Can you verify that all chemicals in use and products you
manufacture are in compliance with the most stringent global
regulatory requirements?
Do you monitor and can you verify that all your suppliers meet
their contractual obligation to comply with final product regulatory
requirements?
Can you verify that you follow a process in which you regularly
review the chemicals used in processes, and/or that can be found
in your products, against published lists to identify chemicals of
concern [e.g., REACH Substance of Very High concern (SVHC),
California Department of Toxic Substances Control DTSC)]?
Can you verify that all chemicals in use and products you manufacture
are in compliance with the most stringent global regulatory
requirements?
Can you verify that you have an established procurement process that
makes MRSL/RSL compliance part of contractual obligations with all
your chemical suppliers?
Can you verify that your facility is in compliance with all of your
customers’ RSLs and do you have a process to implement corrective
actions in case of non-compliance?
Does your facility go beyond compliance with regulations and RSLs and
has it implemented further restrictions on chemicals in use or
chemicals in products? Do you have a documented business process
for this implementation?
Can you verify that you have a valid Certificate of Analysis for each
chemical you use in your facility?
Have you shared the Bill of Chemical Substances (directly or via a third
party) with your customers?
Can you verify that you have a process in place in which you regularly
review the chemicals you use in your processes, and/or that can be
found in your products, against published lists to identify chemicals of
concern (e.g., REACH, SVHC, DTSC)?
Have you provided your suppliers and your customers with consumer
use information about your products, including (un)intended use and
disposal?
Can you verify that you practice a process to assess all chemicals
used to make your products against a defined and transparent set
of human and environmental hazard criteria (e.g., carcinogenic,
mutagenic or toxic for reproduction [CMR], persistent,
bioaccumulative and toxic [PBT], endocrine disruptor [ED]) that
helps to prioritise actions and encourages use of chemicals towards
safer alternatives?
Can you verify that you have a business process that factors hazard
assessments into chemical supplier and procurement decisions?
Can you verify that you have a business process to collaborate with
your supplier to use chemical hazard assessment data combined
with your knowledge of the manufacturing processes to assess the
potential risk of relevant human (worker and consumer) and
environmental exposure routes in your product’s life cycle?
Can you verify that you have a business process in place that factors
your supplier’s risk management actions into supplier selection and
procurement decisions?
Can you verify that you have a business process in place to evaluate
alternatives to determine which are most preferable and to decide
on substitutions or other actions and communicate your decision to
your suppliers and chemical suppliers?
Can you verify that you have a business process in place to use
alternatives assessments to develop and maintain a preferred
substances list?
Can you verify that you have a business process in place to verify
your suppliers’ compliance with your preferred substances list?
Can you verify that you have a business process in place to:
a. Score the sustainability of the chemicals and intermediates
used to make your products?
b. Give priority to those chemicals scoring higher as more
preferable?
Can you verify that you have a business process in place to reward
suppliers who employ sustainable chemistry in the design and
manufacture of their products?
Can you verify that you have a business process in place to score
materials and intermediate products made with more sustainable
production processes (documented and validated)?
Can you verify that you have business goals, metrics and an audit
programme to document the performance and continuous
improvement of your chemicals management and sustainable
chemistry efforts, including public reporting that communicates
progress?
Can you verify that you follow a process to assess all chemicals
used against a defined and transparent set of human and
environmental hazard criteria (e.g., CMR, PBT, ED) that helps to
prioritise actions and encourages use of chemicals towards safer
alternatives?
Can you verify that you have a business process that factors hazard
assessments into chemical supplier and procurement decisions?
Can you verify that you have a business process that uses chemical
hazard assessment data combined with your knowledge of the
manufacturing processes to assess the potential risk of relevant
human (worker and consumer) and environmental exposure
routes in your product’s life cycle?
Can you verify that you have a business process in place that
factors your chemical supplier’s risk management actions into
chemical supplier selection and procurement decisions?
Can you verify that you have a business process in place to verify
the use of preferred substances and compliance from all your
suppliers and communication to your customers
(brands/retailers)?
Can you verify that you have a business process in place to:
a. Score the sustainability of the chemicals and intermediates
you purchase?
b. Give priority to those scoring higher as more preferable?
Can you verify that you have a business process in place to reward
suppliers who employ sustainable chemistry in the design and
manufacture of their products?
Can you verify that you have a business process in place to score
materials and intermediate products made with more sustainable
production processes (documented and validated)?
Can you verify that you have business goals, metrics and an audit
programme to document the performance and continuous
improvement of your chemicals management and sustainable
chemistry efforts, including public reporting that communicates
progress?
Conditions Yes No
2. Does your facility have an individual or team responsible for chemical management or
environmental health and safety?
If so, who?
Do department heads know their responsibilities?
3. Does the facility have an inventory of the hazardous materials used in the facility?
If so, is the inventory electronic or paper? Where is it kept? How often is it updated and by
whom?
4. Are chemicals stored separated by hazard class and compatibility in a uniform storage
system?
Is there sufficient storage area?
5. Has the facility had a comprehensive facility-wide hazardous materials clean out to rid the
business of old, unwanted chemicals? If so, when was the last clean out?
8. Does the facility have Safety Data Sheet (SDS) for the hazardous materials used in the
facility?
Where are these sheets kept? Are they current within the last 3 years?
11. Is the facility properly registered under its applicable generator status of hazardous waste
with the local or regional government?
12. Does the facility have a proper waste management system in place to assure proper
management and disposal of chemicals?
The condition and appropriateness of the chemical storage area, equipment and environmental controls, such as
ventilation systems.
Comments:
Any chemical inventories for these storage areas, the status of these inventories and who maintains them.
Comments:
The location, condition, amount and appropriateness of personal protective equipment (PPE).
Comments:
The location, condition, amount and appropriateness of the emergency response supplies and equipment (e.g.,
fire extinguisher, fire host) for the amount and type of chemicals stored.
Comments:
The location, completeness and availability of Safety Data Sheets (SDSs) in each department using chemicals.
Comments:
Purchasing Yes No
2. One person or department designated with the responsibility of purchasing chemicals (i.e., basic
knowledge of chemistry required).
4. Chemicals purchased in quantities needed for current year only. Rate of use and shelf life considered in
order to minimise purchase quantity.
7. Appropriate means of chemical disposal determined before purchase (i.e., Is disposal as a hazardous waste
required?).
8. Adequate funds for appropriate and legal disposal of the chemical, or its end product, confirmed before
purchase.
10. Proper protective/safety equipment necessary for chemical on hand before purchase.
11. Environmental impact of chemical considered before purchase, (including manufacturing, use and disposal).
Alternatives considered if warranted.
12. Reagents ordered in polyethylene (PE) bottles or plastic coated glass bottles to minimise breakage,
corrosion and rust.
13. A check is made of the chemical inventories in other locations for duplication or excess.
Please complete this form and submit it to the Chemical Management Officer (CMO) for review. The
CMO with the assistance of the Chemical Management Committee will make a final determination
about whether the chemical requested may be purchased. An incomplete response will automatically
be denied.
Name Department_____________________________
Quantity requested
Date_____________________ Date_____________________
11 ZDHC
Priority On Catalogue Order
Room Chemical Factory/ZDHC On Brand's Number/Supplier
Department Building # Product name Chemical Name Chemical Supplier CAS # Quantity Units SDS on file? Hazard Class R Phrase Classes MRSL? RSL? Shelf Life Order Number
Use drop
down arrow Use drop down Use drop down Use drop down Use drop down
to select arrow to select arrow to select arrow to select arrow to select
XYZ Chemical
Dye Weigh House #1 12 Hydrochloric acid (37%) Hydrochloric Acid Company 7647-01-0 2 litres YES Class 8 R 35 N/A No No Jun-15 xxx-xx-xx
ABC Chemical
Dyeing #3 - Glauber's salt Sodium sulfate Company 7757-82-6 1000 kg YES Non-hazardous N/A N/A No No Jun-15 xxx-xx-xx
*This template is for illustrative purposes only. Competent persons undertaking chemical risk assessments may amend this
template to suit site-specific work activities.
Very unlikely Very low risk Very low risk High risk
Very likely Low risk Very high risk Very high risk
Note: These categorisations and the resulting asymmetry of the matrix arise from the examples of harm and likelihood.
Organisations should adjust the design and size of the matrix to suit their needs.
Long-term illness or
1 2 3 4
serious injury
Energy Standards
Management • Factories must have energy usage data available at the factory for the previous 5 full calendar
years. Data must include quantity, heat content and sulfur content information for all fuel types.
Data also must include all electricity use at the factory.
Best Practices
• Factories should develop and implement energy management and conservation procedures for
the factory. The Programme should address the monitoring and review of energy usage, setting
goals and plans for improving energy efficiency and should include provisions for comparing
actual performance against the goals. The Programme should include all processes, lighting,
compressed air systems, heating, ventilation, and air conditioning systems as well as fuel usage
in combustion equipment.
Hazardous Standards
Materials
• Handling, storage and transportation of all hazardous materials at each factory must comply
with all permits and applicable laws and regulations.
• Safety Data Sheets (SDSs) must be on file at the factory for each and every dye, chemical and
chemical product used and stored at the factory. The SDSs must be available for review by all
employees at the factory.
• Factories must have in place procedures to safely receive and handle hazardous materials that
are delivered to the factory.
• Factories must provide physical, chemical and environmental hazard information to transporters
for any hazardous materials transported from the factory.
• Factories must have in place appropriate and adequate spill response equipment and
procedures, in order that any hazardous material spills or releases can be safely and adequately
responded to in a timely manner.
Wastewater Standards
• All discharges from factories must meet limits prescribed by permits and applicable laws and
regulations, whichever is more protective. This standard includes land application of effluents.
• All wastewater and sewage discharges from factories must be properly treated on-site before
being discharged to a receiving stream, or must be discharged under proper authorisation to an
off-site public or private wastewater treatment facility that is operating according to its required
permit, for proper treatment. Untreated wastewater or sewage discharges to the environment
are prohibited.
• Each factory must have all current permits and authorisations required by law for the discharges.
Copies of permits, authorisations and applicable laws, regulations and standards must be on file
at the factory at all times.