Are you doing your lab move right? Not only will this webinar answer this question, it will give you expert insight into a tried lab relocation process. Learn an approach to lab relocation that wil help you reduce your project costs, minimize complications, keep compliance and decrease moving time.
Continual Improvement Plan
1 Purpose
This plan describes the steps to be followed in the establishment, monitoring and periodic review for continual improvement of the project.
2 Responsibility
Name / Designation Contact Number Responsibility
Project Director Promotion and monitor implementation of the plan and provide necessary resources.
Sr. Project Manager Support and monitor implementation of the plan and provide necessary resources.
HSE Manager Facilitate implementation of the plan.
Construction Manager Attends to action/s as required.
MEP Manager Attends to action/s as required.
Logistic Manager Attends to action/s as required.
3 KPI’s and Objectives
Set KPI’s and objectives will be reviewed on monthly basis. This will be done in accordance with Health and Safety Plan.
4 Mobilization / Office Set-up
Within the plot of land obtained from the Client for the purposes of establishing the Site Compound, will setup the Site Offices and laydown areas.
In addition, Temporary site and satellite offices as well as rest areas will be installed.
Innovation Strategy
The temporary site office and mobile rest areas will be equipped with solar panels as part of our innovation strategy.
The initiative was developed to provide an ECO welfare shelter for workers, a shaded area with cold drinking water and rotating fans. All of which is to be made available in a mobile containerized energy sufficient solution, that provides a friendly comfortable environment for workers on site.
5 Method Statement and Risk Assessment (MSRA)
Method Statements and Risk Assessment describing in detail the way a work task or process is to be completed shall be submitted for Consultant review and approval. The MSRA shall outline the hazards involved and include a step by step guide on how to do the job safely.
The MSRA shall also detail which control measures have been introduced to ensure the safety of anyone who is affected by the task or process.
6 Don’t Walk By
HSE system that provides triplicate self-carbonating pocket-sized booklets to be issued and explained to the nearest responsible supervisor whenever an unsafe act or condition is noticed.
Innovation Strategy
Currently the system use triplicate self-carbonating pocket-sized booklets (hard copy), this will be converted into electronic tools that could be utilized through tablet, android and smart phones as part of our innovation strategy. The process is in progress and is expected to be finalized soon.
7 Review and Update
Reviews and updates shall be conducted on Health and Safety Plan and all other safety related plans included in the deliverables in accordance to the frequency stipulated in the plans or whenever necessary.
TOOL BOX TALK | PERMIT TO WORK (PTW) SYSTEM
This TBT is written to refresh all personnel on how a Permit to Work (PTW) system works and the reasons why a PTW system will operate on the site you are working on.
It is not designed to replace any individual site specific PTW training you may receive.
What is Gemba?
For those who haven’t heard the term Gemba before, it is a Japanese word that means “The Real Place,” and is used in this context to refer to any area of a company where the action is taking place. This could be a warehouse where products are stored and shipped, or
a facility where products are made, or even a customer service area. Anywhere that action is taken and value is created in support of the business is considered Gemba.
So, a Gemba walk is when business leaders leave their offices and go out to see how things are done, and ideally, find ways to make improvements. Managers can get out and observe work from the ‘front lines’ rather than simply reviewing reports or listening to observations of others from behind their desks.
Continual Improvement Plan
1 Purpose
This plan describes the steps to be followed in the establishment, monitoring and periodic review for continual improvement of the project.
2 Responsibility
Name / Designation Contact Number Responsibility
Project Director Promotion and monitor implementation of the plan and provide necessary resources.
Sr. Project Manager Support and monitor implementation of the plan and provide necessary resources.
HSE Manager Facilitate implementation of the plan.
Construction Manager Attends to action/s as required.
MEP Manager Attends to action/s as required.
Logistic Manager Attends to action/s as required.
3 KPI’s and Objectives
Set KPI’s and objectives will be reviewed on monthly basis. This will be done in accordance with Health and Safety Plan.
4 Mobilization / Office Set-up
Within the plot of land obtained from the Client for the purposes of establishing the Site Compound, will setup the Site Offices and laydown areas.
In addition, Temporary site and satellite offices as well as rest areas will be installed.
Innovation Strategy
The temporary site office and mobile rest areas will be equipped with solar panels as part of our innovation strategy.
The initiative was developed to provide an ECO welfare shelter for workers, a shaded area with cold drinking water and rotating fans. All of which is to be made available in a mobile containerized energy sufficient solution, that provides a friendly comfortable environment for workers on site.
5 Method Statement and Risk Assessment (MSRA)
Method Statements and Risk Assessment describing in detail the way a work task or process is to be completed shall be submitted for Consultant review and approval. The MSRA shall outline the hazards involved and include a step by step guide on how to do the job safely.
The MSRA shall also detail which control measures have been introduced to ensure the safety of anyone who is affected by the task or process.
6 Don’t Walk By
HSE system that provides triplicate self-carbonating pocket-sized booklets to be issued and explained to the nearest responsible supervisor whenever an unsafe act or condition is noticed.
Innovation Strategy
Currently the system use triplicate self-carbonating pocket-sized booklets (hard copy), this will be converted into electronic tools that could be utilized through tablet, android and smart phones as part of our innovation strategy. The process is in progress and is expected to be finalized soon.
7 Review and Update
Reviews and updates shall be conducted on Health and Safety Plan and all other safety related plans included in the deliverables in accordance to the frequency stipulated in the plans or whenever necessary.
TOOL BOX TALK | PERMIT TO WORK (PTW) SYSTEM
This TBT is written to refresh all personnel on how a Permit to Work (PTW) system works and the reasons why a PTW system will operate on the site you are working on.
It is not designed to replace any individual site specific PTW training you may receive.
What is Gemba?
For those who haven’t heard the term Gemba before, it is a Japanese word that means “The Real Place,” and is used in this context to refer to any area of a company where the action is taking place. This could be a warehouse where products are stored and shipped, or
a facility where products are made, or even a customer service area. Anywhere that action is taken and value is created in support of the business is considered Gemba.
So, a Gemba walk is when business leaders leave their offices and go out to see how things are done, and ideally, find ways to make improvements. Managers can get out and observe work from the ‘front lines’ rather than simply reviewing reports or listening to observations of others from behind their desks.
Making process improvement results concrete and tangible is not that hard to do and can help quantify measurable results for not just individual projects but for an entire continuous improvement program. Although each organization may support different kinds of savings, we will share a general approach to help you quantify savings for your improvement project including hard and soft dollar savings.
6S (previously known as 5S) is a visual system for improvement that helps create and maintain an organised, clean, high performance workplace. It forms the basis for standards work, which enables you to measure improvements. The extra ‘S’ was added to the 5S Lean tool to emphasise the importance of safety. The 6S stands for:
o 1. Sort: remove what is not needed
o 2. Set in order: agree what goes where and make easily accessible
o 3. Shine: keep the environment clean
o 4. Standardise: a consistent process agreed by all
o 5. Sustain: continually improve.
o 6. Safety: identify and prevent unsafe conditions
Using 6S will help you to reduce the opportunity for variability in activities by ensuring that everything needed at each step of the process is easily available. This means that any defect in a particular step is easier to see.
This "Brief Guide" gives information on the Employee Handbook or Staff Handbook including list of policies and procedures required by law, those recommended highly so as to enable a company to defend itself and finally, discretionary policies. This document can be downloaded at http://www.collierbroderick.ie/Services/HR%20Compliance/Employee%20Handbook.asp
This slide is related to Good documentation Practice in Pharmaceutical Industries. It was presented in the pharmaceutical industry (Chemidrug Industry Private Ltd.) during the training session.
Good Document Control Practices and Procedures: ISO 9001:2015Qualsys Ltd
Read More: quality.eqms.co.uk/eqms-governance-risk-compliance-software-datasheets
Once upon a time, records lived in lever arch-files, filing cabinets and in cardboard boxes. All key documents and records were strictly guarded under lock-and-key by those who knew the rules, and applied them assiduously.
Nowadays, records exist all over the business, well beyond the reach of the traditional warden. With everything digital, records are stored on desktops or mobile devices, on clouds or on servers, on intranets or on social media.
But what impact has this decentralisation of records had on organisations?
In this fast paced, mobile world, documentation is created at break-neck pace.
Not only has the internet, remote working and globalisation completely changed the way documents are created, it has transformed how records are exchanged, viewed, interrogated and collaborated upon.
Despite the issues with lost company records, only a third of organisations feel their document control procedures are integrated enterprise-wide, according to an AIIM Industry Report.
Two in three organisations feel they have failed to integrate document control procedures across the organisation, or have little or no document control policy at all.
Not only do these companies risk litigation costs, loosing customer confidence, bad publicity and loosing confidential customer information, they are failing to exploit important knowledge resources.
EQMS Document Manager helps you to keep control of records. EQMS enables you to:
control access and usage of documented information, as well as the distribution and retrieval of documents.
Follow a systematic approach: e.g. follow the Plan > Do > Check > Act cycle.
Retain records: have documents to prove that you have done what you said you would do.
This supports organisations to meet the requirements of ISO 9001:2015 and other management standards.
This presentation will explore how Celgene a global biopharmaceuticals company has connected talent management with technology to place large, complex and critical spend categories such as Marketing, SG&A, and R&D under management by procurement.
Making process improvement results concrete and tangible is not that hard to do and can help quantify measurable results for not just individual projects but for an entire continuous improvement program. Although each organization may support different kinds of savings, we will share a general approach to help you quantify savings for your improvement project including hard and soft dollar savings.
6S (previously known as 5S) is a visual system for improvement that helps create and maintain an organised, clean, high performance workplace. It forms the basis for standards work, which enables you to measure improvements. The extra ‘S’ was added to the 5S Lean tool to emphasise the importance of safety. The 6S stands for:
o 1. Sort: remove what is not needed
o 2. Set in order: agree what goes where and make easily accessible
o 3. Shine: keep the environment clean
o 4. Standardise: a consistent process agreed by all
o 5. Sustain: continually improve.
o 6. Safety: identify and prevent unsafe conditions
Using 6S will help you to reduce the opportunity for variability in activities by ensuring that everything needed at each step of the process is easily available. This means that any defect in a particular step is easier to see.
This "Brief Guide" gives information on the Employee Handbook or Staff Handbook including list of policies and procedures required by law, those recommended highly so as to enable a company to defend itself and finally, discretionary policies. This document can be downloaded at http://www.collierbroderick.ie/Services/HR%20Compliance/Employee%20Handbook.asp
This slide is related to Good documentation Practice in Pharmaceutical Industries. It was presented in the pharmaceutical industry (Chemidrug Industry Private Ltd.) during the training session.
Good Document Control Practices and Procedures: ISO 9001:2015Qualsys Ltd
Read More: quality.eqms.co.uk/eqms-governance-risk-compliance-software-datasheets
Once upon a time, records lived in lever arch-files, filing cabinets and in cardboard boxes. All key documents and records were strictly guarded under lock-and-key by those who knew the rules, and applied them assiduously.
Nowadays, records exist all over the business, well beyond the reach of the traditional warden. With everything digital, records are stored on desktops or mobile devices, on clouds or on servers, on intranets or on social media.
But what impact has this decentralisation of records had on organisations?
In this fast paced, mobile world, documentation is created at break-neck pace.
Not only has the internet, remote working and globalisation completely changed the way documents are created, it has transformed how records are exchanged, viewed, interrogated and collaborated upon.
Despite the issues with lost company records, only a third of organisations feel their document control procedures are integrated enterprise-wide, according to an AIIM Industry Report.
Two in three organisations feel they have failed to integrate document control procedures across the organisation, or have little or no document control policy at all.
Not only do these companies risk litigation costs, loosing customer confidence, bad publicity and loosing confidential customer information, they are failing to exploit important knowledge resources.
EQMS Document Manager helps you to keep control of records. EQMS enables you to:
control access and usage of documented information, as well as the distribution and retrieval of documents.
Follow a systematic approach: e.g. follow the Plan > Do > Check > Act cycle.
Retain records: have documents to prove that you have done what you said you would do.
This supports organisations to meet the requirements of ISO 9001:2015 and other management standards.
This presentation will explore how Celgene a global biopharmaceuticals company has connected talent management with technology to place large, complex and critical spend categories such as Marketing, SG&A, and R&D under management by procurement.
How closely does Environmental, Health, and Safety (EH&S) monitor chemicals with the potential to form peroxides within the laboratories of your company? How well aware are your researchers of which chemicals these are and how to handle and dispose of them? Proper management of potential peroxide-forming solvents is vital to the safety of your researchers and facility staff, the compliance of your institution, the maintenance of your laboratory peroxide-forming chemical equipment and research materials, and the cost of your waste disposal. Take a look to find out everything you need to know about the hazards and handling of advanced peroxide forming chemicals.
Learn about the regulations surrounding the Clean Air Act and how to remain in compliance with them. This presentation covers:
Which regulations apply to your institution
How to meet recording and reporting requirements
Tactics for keeping compliant with all necessary regulations
Wednesday 14 October 2015 was a red letter day in the history of the Caribbean Examinations Council (CXC). It was the day CXC officially opened its own home, the new CXC Headquarters. This issue commemorates the opening of the CXC Headquarters
with some of the speeches and plenty of the photographs from the big day. It also celebrates the academic achievements of the 2015 Regional Top Awardees and their momentous trip Belize to receive their prizes and chronicles their “UnBelizable” experience.
Opportunity for healthcare and insurance sector investor. Attach pdf will introduce you the UAH (united Africa Health) health innovation - Smart integrated digital health kiosk features and project overview .
Africa's 1st digital health care & wellness clinic kiosk start up .
The "New Normal" of Africa Health care : UAH smart e- clinic & prevention care hub.
How UAH smart e- clinic kiosk is fixing Africa Chronic disease challenge , enabling convenient and data driven digital health care experience?
This presentation teaches:
How to prepare for and react during an emergency response situation.
A variety of scenarios including but not limited to mercury spills, unstable chemicals, water/sewer line breaks, oil spills and more.
How to create and implement plans and trainings prior to an emergency response situations
What information you should provide to a responding contractor.
What to expect when they arrive.
This presentation addresses the various emergency response scenarios and critical information you need to know when preparing for an ER. You will learn about fascinating ER calls, worst case versus best case and get lessons learned so you are fully prepared should an incident occur.
This webinar provided an overview of how to effectively manage peroxide formers, beginning with training and identification. Our expert shared real-world examples of institutions that have struggled with and rectified their peroxide former problems.
This presentation addresses the various drivers for environmental PM, as well as best practices for implementing an inspection-based PM program and calendar. Find out who the regulators are and how to ensure compliance with these cost-saving techniques.
Managing sharps and regulated medical waste (RMW) can be a costly and complicated process for healthcare facilities. Staying OSHA and RCRA compliant is a top priority, in addition to keeping costs down and operational efficiency up. This presentation provides information on how to revamp your program in a way that streamlines your RMW process to boost safety, efficiency and cost savings.
This presentation offers guidance to those hospitals that are rolling out a new pharmacy program as well best practices for maintaining and continuously improving current programs. Take a look and find out why annual program reviews are highly recommended.
This presentation addressing the various aspects of lab relocation, from building project teams and pre-project planning to managing hard and soft infrastructure. Learn how to maintain business continuity throughout the entire process.
Webinar presentation regarding waste stream analysis and best management practices. This presentations covers tactical topics including how to thoroughly and expediently analyze your own waste streams. It includes real life tactics for cost-efficient waste stream management.
This presentation details how to reduce liability through lab decommissioning. The presentation will teach you what factors to look out for when considering your liability as it applies to a decommissioning as well as best practices and the steps you need to take to assure your organization is protected.
Expert Ian Lanza shared tips and tricks for executing a safe and efficient laboratory relocation. Topics of focus included: Maintaining business continuity during your move, fulfilling lease obligations, and obtaining regulatory licenses, permits and other programs.
Have an upcoming decommissioning project? Check out these slides for methods and best practices to executing a successful laboratory move, renovation or closure. Our expert, Craig Sasse, shares his experience managing multiple decommissioning projects.
Despite having a full team in place, do you feel you are still not in control of your hazardous waste programs? Do you fall short on meeting department goals? There are several key elements to managing a high-level and elite program with less added cost than you might assume. Reducing cost, improving compliance and sustainability, while maximizing safety are some of the key components to include in all programs.
Everything You Need to Know About Planning and Executing Your Next Laboratory...Triumvirate Environmental
At the end of your laboratory relocation, it is necessary to ensure the old lab space is properly decontaminated and that the decontamination is properly documented. Thorough decontamination and documentation is necessary to ensure there is no contamination and all lease requirements are fulfilled when moving lab spaces. During this webinar, you will learn about managing the decommissioning and decontamination of spaces and equipment and how to make sure no environmental liability remains.
Despite having a full team in place, do you feel you're still not in control of your hazardous waste programs? Do you completely understand how your organization manages waste and the impacts associated with it? Do you fall short on meeting department goals? Are you tracking the right metrics that will increase your organization’s sustainability? There are several key elements to managing a high-level and elite program with less added cost than you might assume. Reducing cost, improving compliance and sustainability - while maximizing safety - are some of the key components to include in all programs.
Laboratories have traditionally collected liquid chemical waste in glass containers without much regard to the potential risks. Unfortunately, this often results in broken collection containers and the release of hazardous, non-compliant vapors into the air. As a way to provide an increased level of safety, compliance, and efficiency, Triumvirate has found a new solution to these traditional methods in the VOCLok.
Laboratories have traditionally collected liquid chemical waste in glass containers without much regard to the potential risks. Unfortunately, this often results in broken collection containers and the release of hazardous, non-compliant vapors into the air. As a way to provide an increased level of safety, compliance, and efficiency, Triumvirate has found a new solution to these traditional methods in the VOCLok.
Laboratories have traditionally collected liquid chemical waste in glass containers without much regard to the potential risks. Unfortunately, this often results in broken collection containers and the release of hazardous, non-compliant vapors into the air. As a way to provide an increased level of safety, compliance, and efficiency, Triumvirate has found a new solution to these traditional methods in the VOCLok.
Electronics recycling webinar final presentationNimonik
Electronic recyclers are experiencing demands that are difficult to meet in today’s ever-changing regulatory environment.
To help, Nimonik invited Ronald Lepore, a former RQO auditor, to discuss:
1- Common non-conformances during government and certification audits
2- Operational bottlenecks and best practices; with case studies
3- How to adapt to the changing trends
Everything You Need to Know About Planning and Executing Your Next Laboratory...Triumvirate Environmental
Laboratory relocations are inherently disruptive to an organization and can be hectic given how many people in the organization are affected, and the number of stakeholders required to pull off a successful relocation. Like any project, lab relocations require strong and competent project management to be successful in reducing the impact to the organization.
This presentation reviews existing methods for solvent waste collection and the drawbacks that are present, including compliance, VOC exposure and cost. Our speaker introduces a new system designed by Triumvirate Environmental that addresses these limitations. Find out how the VOCLok is installed and maintained and how other companies have benefited from migrating to this system.
This presentation provides insight into how to manage peroxide formers in a streamlined, cost effective way. You will learn how to create and implement a peroxide former management plan and see how other institutions have rectified their peroxide former problems through multiple case studies and real-world scenarios.
Similar to Lab Relocation: Is Your Facility Prepared? (20)
How to Prepare for and Respond to a Confirmed COVID-19 Case at Your Lab or Ma...Triumvirate Environmental
As essential businesses continue to operate, it’s crucial to consider how to handle a confirmed COVID-19 case in the workplace. Despite safety precautions to avoid the spread, one of your employees may get sick – do you know what to do? The COVID-19 pandemic has drastically altered how we work and operate. Take a proactive approach to safely keep your business operational in the event of a confirmed COVID-19 case by developing sound disinfection policies and procedures.
ISO auditing leads to improved company EHS culture, consistency, and team focus. When organizations conform to these ISO standards and obtain third-party ISO certification, it authenticates that they utilize standardized management systems to continuously improve Occupational Health and Safety and Environmental performance.
Does your organization need an industrial hygiene program? Are you looking to create a program but don’t know where to start? Industrial hygiene allows you to anticipate, evaluate and control environmental factors that impact people’s health. Critical to environmental health and safety, an industrial hygiene program is important not only for regulatory compliance but also to maintain your public relations and reputation.
The deadlines for Tier II Reports, Biennial Reports, and OSHA 300 Logs are all fast approaching. Are you prepared to file all your necessary reports in time? It is important to take the time to carefully review your facility to determine your requirements for these regulatory reports.
Cannabis growers, cultivators, and distributors face unique compliance challenges when navigating federal and state regulations, managing hazardous and non-hazardous waste streams, and ensuring your facility runs safely and compliantly. This webinar will help early-stage and fast-growing cannabis companies understand the state and federal regulatory environment, obtain permits and licenses, and build environmental, health, and safety (EH&S) programs. Whether your cannabis organization is new to the compliance world or has some safety programs in place, this webinar will provide guidance on how to reach operational excellence.
The Key Elements of Building an OSHA-Compliant Workplace from the Ground UpTriumvirate Environmental
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In September, OSHA released its latest “Top 10” list of most frequently cited workplace violations. Hear our expert analyze the most common OSHA violations and the overall state of EHS regulatory compliance in 2019.
2019 Healthcare Accreditation Regulatory Updates: How Do the New Regulations ...Triumvirate Environmental
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Oil spills present real public health and environmental concerns. In response to these concerns, the EPA created rules around SPCC. The EPA’s SPCC rules are meant to prevent oil discharge from entering navigable waters and/or adjoining shorelines.
There have been many recent changes to the DEA and EPA regulations regarding pharmaceutical waste management. Is your organization compliant with the current rules? Here is a comprehensive look at the disposal and onsite waste management regulations for controlled substances.
Measuring the Success of Your EHS Program: Are You Tracking These Key Perform...Triumvirate Environmental
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There are over 90 biotechnology and pharmaceutical laboratories located within the Cambridge city limits. With such a high concentration of labs, the city has stringent regulations to contain exposure risks and ensure that the community is safe. In this session, the Department of Public Health will discuss lab safety in the city. Join us to gain a more comprehensive understanding of Massachusetts and Cambridge regulations to ensure you are running a safe and compliant lab.
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Recently the National Safety Council collaborated with three Campbell Institute members to understand the role fatigue plays in their operations at selected locations. Research participants took part in a two-part survey consisting of an operational needs assessment and an employee survey.
Does your organization run internal audits regularly? Prepare for a regulator to come knocking at your door by catching areas of non-compliance before the inspector can. Internal audits allow you to identify gaps in your existing EHS programs and improve processes before an official inspection, so you can be confident in your audit-readiness.
Despite well-defined requirements, procedures, and targets, many organizations still struggle with delivering well-defined, exceptional EHS compliance programs. A strong external partnership can reposition your EHS compliance program and drive strong operational and financial outcomes. But once you decide to establish an EHS partnership, how do you ensure you are getting the most out of it?
Chemical inventory management is often a confusing and labor-intensive exercise. This webinar sheds light on how to build, operationalize, and improve a chemical inventory program. We will dissect the many nuances of a chemical inventory, and offer innovative, service-based solutions to help you successfully manage your chemical inventory program.
OSHA Compliance: Ensuring Laboratory & Manufacturing Safety at Your WorksiteTriumvirate Environmental
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Does your facility have a fully compliant environmental program? Are you prepared for your next EPA audit? In this session, you will receive a comprehensive overview of the EPA and the components needed to create a compliant environmental program for your workplace. We will cover environmental compliance in both laboratory and manufacturing settings.
Personal Brand Statement:
As an Army veteran dedicated to lifelong learning, I bring a disciplined, strategic mindset to my pursuits. I am constantly expanding my knowledge to innovate and lead effectively. My journey is driven by a commitment to excellence, and to make a meaningful impact in the world.
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Cultivating and maintaining discipline within teams is a critical differentiator for successful organisations.
Forward-thinking leaders and business managers understand the impact that discipline has on organisational success. A disciplined workforce operates with clarity, focus, and a shared understanding of expectations, ultimately driving better results, optimising productivity, and facilitating seamless collaboration.
Although discipline is not a one-size-fits-all approach, it can help create a work environment that encourages personal growth and accountability rather than solely relying on punitive measures.
In this deck, you will learn the significance of workplace discipline for organisational success. You’ll also learn
• Four (4) workplace discipline methods you should consider
• The best and most practical approach to implementing workplace discipline.
• Three (3) key tips to maintain a disciplined workplace.
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Explore our most comprehensive guide on lookback analysis at SafePaaS, covering access governance and how it can transform modern ERP audits. Browse now!
3. 1. All lines are muted, use the chat panel for tech issues.
2. Q&A at the end. Type questions into “questions” pane
in the chat panel.
3. Unanswered questions will be answered via email after
the webinar.
4. Webinar recording and slides will be emailed to you
this afternoon.
Share With the Audience
4. Meet Your Presenter
• Ian Lanza,
• Triumvirate Environmental – Regional
Life Sciences Director
• Triumvirate Employee: 8 Years
• Focus on: sustainability, environmental
and safety performance
• Works with: premier biotech and
pharmaceutical companies
• Contact:
• Email: ilanza@triumvirate.com
• Cell Phone: 802-522-9036
10. Control the Chaos
• Stakeholder Map and
Expectations
• Relocation Team
• Project Plan
• Regular Relocations
Meetings
11. Managing Stakeholders
• Identify all stakeholders
• Internal
• External
• Regulatory
• Understand needs and
expectations of each
stakeholder
• How will this impact
• Time
• Budget
• Logistics
12. Assemble a Relocation Team
• Assemble a team based on
your stakeholder map
• Select representatives from
key or important stakeholder
groups
• Don’t forget to include external
stakeholders
13. Build a Project Plan
• Have the relocation team build
(or review) a project plan using
the stakeholder map
• Critical path planning
• Risk Management
• Identify risk by stakeholder group
and project phase
14. Relocation Meetings
• Schedule routine relocation
meetings with the team to
discuss the plan. The plan
will evolve throughout the
planning period.
• Agenda
• Minutes
• Frequency
15. Project Phases
Phase VI – EHS Programs and Systems
Phase V – Permits and Licensing
EHS Programs/ Permits/ Licenses Other
Phase IV – Closure Assessment
Hazardous Materials Other
Phase III - Decontamination
Lab Spaces Non Lab Spaces
Phase II – Move
Hazardous Material Move Equipment, Furniture Move
Phase I – Disposal
Chemical Disposal Consumable/ equipment disposal
Phase 0 – Design
Hazardous Material Flow Facility Design and Engineering
16. Facility Move Project Schedule
Disposal
Chemical
Move
Decontamination
Closure
Assessment
Permitting
and Plans for
New Space
Training and EH&S Program
Implementation and
Maintenance
Existing
FacilitySpace
NewFacility
Space
Time Axis
Design
18. Phase 0: Design
• Engage relocation stakeholders
• Building design
• Material flow
• Engineering controls
This will improve business continuity throughout
the entire design, build, relocation project.
20. Phase 1: Discard Unwanted
Materials
Discard materials
that are:
Wastes
Expired materials
Irrelevant materials
Consider
Risk of moving material
vs. disposing and buying
new
Regulatory obligations for
moving and disposing of
material
Moving materials that have no impact on the new operations
(larger or smaller) present unnecessary risks and costs
21. Other Materials To Be Discarded
• Chemicals
• Electronics
• Equipment
• Furniture
• Consumables
• Municipal waste
Try to remove as much material prior
to the move as possible. In order to
exit your lease EVERYTHING will
need to be out!
23. Phase 2: Move
Identify the materials
and equipment
Regulatory obligations
Risks of moving the
material
High Risk Material
What’s
Moving?
24. Phase 2: Move
Refer to your critical path planning in the project plan
Time Management
What is the projected operational down time?
What is the schedule…when will what be moved?
Don’t forget about prep time!!
Logistics Management
Where are materials going? - Will they all fit?
Will labs be consolidated, split, or is it a one for one move?
Physical spaces
25. Phase 2: Move
• Work out logistics prior to the move:
• Access
• Locations (cold material, flammables, power)
• Critical Path Planning – is there an order of
when equipment, supplies, and furniture are
delivered?
• Have someone present from the relocation
team to ensure you everything is brought to
the proper space.
27. Phase 3: Decontamination
Determine “Performance
Standard”
Identify potential contaminates
Identify obligations in lease
agreement and regulatory
requirements.
Limit liability through best
management practices.
Develop a decontamination plan to
establish scope, means and methods,
confirmation of clean.
29. How Clean is Clean?
• Lease Language
• Property Owner
Expectation
• The American National
Standard/AIHA Z9.11–2008
• Organizational Standards
• Organizational risk
tolerance
30. Decontamination Plan
• Work with key stakeholder to develop a
decontamination plan.
• This may include prior sampling to determine
level of contamination or identify higher risk
areas prior to beginning.
• Clearly articulate scope and methods.
Complete this well before the relocation and
decontamination efforts begin. You should be able to
begin the decon as soon as the move is completed.
33. Phase 4: Closure Assessment
Document and ensure the removal of all hazardous
materials and other environmental hazards
Approve and confirm decontamination methods of all
spaces
Confirm ‘Clean’ through quantitative methods
Terminate all permits and licenses
Document and report the entire closure process
The facility closure report must be signed and
approved by a qualified individual
34. Phase 4: Lab Closure
Reports limit potential
liability when occupying,
leasing or leaving space.
Plans depicting areas
assessed
Document the cleaning
procedures
Photographic
documentation
Visual observations.
Include damage and “wear
and tear”
Clearance sampling
documentation
Review of plan
requirements and
deviations
QA/QC review
Waste disposal paperwork
Statement of “Acceptable
Level of Risk”
Signed by “Qualified
Individual”
36. Phase 5: Permits and Licenses
1.Remove materials
2.Notify the regulatory
agency of permit/ license
termination
3.Provide paperwork and
documentation to ensure
materials were removed
1.Identify the need for new
permits/ licenses
2.Establish controls and
programs for the permit/
license may require
3.Apply for the permit prior to
moving to the new facility
Old Facility – Terminate
permits and licenses
New Facility – Obtain new
permits and licenses
Begin the
process early!!
39. Phase 6: EH&S Programs and
Systems
Plan ahead
• Some permits take time to obtain
• Implement new engineering controls, where necessary
Roll out the new programs and systems as part of
the new operating facility
Establish expectations and standards from Day-1
Communicate the new EH&S programs, systems
and expectations through training within the
month of moving
40. Summary
• Relocation projects are complex because of the
number of stakeholders impacted and the number
of stakeholders to complete the project successfully
• PPPPP
• Think of a relo as part of a
much larger project (design,
build, relo, new programs)