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.
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.
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.
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.
Supplementing lab analysis with inline quality measurements in food Industryola wesstrom
White paper describing various ideas how instrumentation can be used to supplement traditional lab measuerments to improve production yield, reduce re-work and to improve productivity of lab personnel in food industry
You will hear about an LLNL developed high-efficiency filter made from ceramic materials in a metal housing. The filters are scalable and can be engineered for myriad commercial applications.
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.
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.
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.
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.
Supplementing lab analysis with inline quality measurements in food Industryola wesstrom
White paper describing various ideas how instrumentation can be used to supplement traditional lab measuerments to improve production yield, reduce re-work and to improve productivity of lab personnel in food industry
You will hear about an LLNL developed high-efficiency filter made from ceramic materials in a metal housing. The filters are scalable and can be engineered for myriad commercial applications.
Learn about the benefits of including inline instrumentation in your food plant or related business. This high quality white paper describes what you need to know to get the most out of utilizing inline analyzers including how they can provide:
Improved Reliability
Seamless Integration
Simplified Calibration
As well as, how to get started in getting your business prepared for inline instrumentation.
Continuous Flow Chemistry And The Manufacture Of Active Pharmaceutical Ingr...Stuart Silverman
A Series Of Informative Disquisitions About Continuous Flow Chemistry
Part Three:
Translation of flow protocols from the bench to the plant
Reaction Classes
Workup and isolation
Life Cycle Management of Chromatographic Methods for BiopharmaceuticalsWaters Corporation
The development and manufacture of biopharmaceuticals is a dynamic and rapidly growing industry. By the nature of their production, biopharmaceuticals are highly complex heterogeneous mixtures that require many analytical techniques for characterization and routine testing. As a result, many manufacturers incorporate life cycle management into their respective workflows to take advantage of newer technologies and methodologies to ensure efficacy and patient safety.
In this presentation, we will address the range of chromatographic categories – HPLC, UHPLC, and UPLC – and define the characteristics associated with each. The discussion will continue with several examples of methods transferred from legacy HPLC instrumentation to modern UHPLC and UPLC instruments. We will compare qualitative and quantitative data across each chromatographic class. Resolution, sensitivity, and overall run time will be used as metrics to assess the success of the method transfer to the respective LC platform, to ensure the transferred methods are in line with current acceptance criteria.
Learn:
- The importance of selecting the correct instrumentation to meet user needs.
- Which parameters influence method transfer from one LC platform to another.
- How workflows can benefit from features such as Multi-flow path technology and Gradient SmartStart when transitioning methods.
Interested in more detail? Watch the related on-demand webinar: http://view6.workcast.net/register?pak=3479247014905635
15-20 August 2016. Kenya. AFLANET: Aflatoxin Networking on Aflatoxin Reduction in the Food Value Chain. The goal of this project is to establish a long-term network be-tween scientific and development partners in Kenya/East Africa and Germany to address the reduction of aflatoxins in the food value chain. It is funded by German Ministry for Food and Agriculture (BMEL) (Project Duration: 01.07.2016 - 31.07.2017).
Understanding the Impact of Chromatographic System Dispersion on Separation P...Waters Corporation
The last 10 years have seen substantial improvements in both chromatographic columns and instrumentation that have enabled faster and more efficient separations. The once common 4.6 x 150 mm column packed with 5 µm particles has been gradually replaced by smaller columns packed with smaller solid-core particles. To maximize the performance of these highly efficient solid-core particles one must understand the impact that instrument dispersion has on the chromatographic separation.
Presentation on the examination of microbiological data for assessment and trending.
Includes: normalizing data, graphs, and assessment of alert and action levels.
Webinar - Pharmacopeial Modernization: How Will Your Chromatography Workflow ...Waters Corporation
In this webinar, Dr. Leonel Santos and Dr. Horacio Pappa from the United States Pharmacopeia (USP) will provide an overview of its pharmacopeial harmonization and modernization efforts. The pair will also review changes described in the pending USP General Chapter <621> on liquid chromatography (LC), which will provide increased flexibility for gradient methods.
Amanda Dlugasch, from Waters Corporation, will follow with an illuminating case study, which leverages USP <621> allowable adjustments to illustrate the benefits of modernizing methods, including migrating HPLC methods to UHPLC or UPLC, without the need to revalidate.
Topics covered in this webinar will include:
- Pharmacopeial monograph modernization prioritization scheme
- Review of USP General Chapter <621> current allowable adjustments to validated chromatographic methods and forthcoming updates
- Case study on the migration of isocratic and gradient pharmacopeial methods to modern chromatography column technology, highlighting improved method performance and throughput
Replay the webinar, hosted by SelectScience:
https://www.selectscience.net/webinars/pharmacopeial-modernization-how-will-your-chromatography-workflow-benefit/?webinarID=1228
Learn about the benefits of including inline instrumentation in your food plant or related business. This high quality white paper describes what you need to know to get the most out of utilizing inline analyzers including how they can provide:
Improved Reliability
Seamless Integration
Simplified Calibration
As well as, how to get started in getting your business prepared for inline instrumentation.
Continuous Flow Chemistry And The Manufacture Of Active Pharmaceutical Ingr...Stuart Silverman
A Series Of Informative Disquisitions About Continuous Flow Chemistry
Part Three:
Translation of flow protocols from the bench to the plant
Reaction Classes
Workup and isolation
Life Cycle Management of Chromatographic Methods for BiopharmaceuticalsWaters Corporation
The development and manufacture of biopharmaceuticals is a dynamic and rapidly growing industry. By the nature of their production, biopharmaceuticals are highly complex heterogeneous mixtures that require many analytical techniques for characterization and routine testing. As a result, many manufacturers incorporate life cycle management into their respective workflows to take advantage of newer technologies and methodologies to ensure efficacy and patient safety.
In this presentation, we will address the range of chromatographic categories – HPLC, UHPLC, and UPLC – and define the characteristics associated with each. The discussion will continue with several examples of methods transferred from legacy HPLC instrumentation to modern UHPLC and UPLC instruments. We will compare qualitative and quantitative data across each chromatographic class. Resolution, sensitivity, and overall run time will be used as metrics to assess the success of the method transfer to the respective LC platform, to ensure the transferred methods are in line with current acceptance criteria.
Learn:
- The importance of selecting the correct instrumentation to meet user needs.
- Which parameters influence method transfer from one LC platform to another.
- How workflows can benefit from features such as Multi-flow path technology and Gradient SmartStart when transitioning methods.
Interested in more detail? Watch the related on-demand webinar: http://view6.workcast.net/register?pak=3479247014905635
15-20 August 2016. Kenya. AFLANET: Aflatoxin Networking on Aflatoxin Reduction in the Food Value Chain. The goal of this project is to establish a long-term network be-tween scientific and development partners in Kenya/East Africa and Germany to address the reduction of aflatoxins in the food value chain. It is funded by German Ministry for Food and Agriculture (BMEL) (Project Duration: 01.07.2016 - 31.07.2017).
Understanding the Impact of Chromatographic System Dispersion on Separation P...Waters Corporation
The last 10 years have seen substantial improvements in both chromatographic columns and instrumentation that have enabled faster and more efficient separations. The once common 4.6 x 150 mm column packed with 5 µm particles has been gradually replaced by smaller columns packed with smaller solid-core particles. To maximize the performance of these highly efficient solid-core particles one must understand the impact that instrument dispersion has on the chromatographic separation.
Presentation on the examination of microbiological data for assessment and trending.
Includes: normalizing data, graphs, and assessment of alert and action levels.
Webinar - Pharmacopeial Modernization: How Will Your Chromatography Workflow ...Waters Corporation
In this webinar, Dr. Leonel Santos and Dr. Horacio Pappa from the United States Pharmacopeia (USP) will provide an overview of its pharmacopeial harmonization and modernization efforts. The pair will also review changes described in the pending USP General Chapter <621> on liquid chromatography (LC), which will provide increased flexibility for gradient methods.
Amanda Dlugasch, from Waters Corporation, will follow with an illuminating case study, which leverages USP <621> allowable adjustments to illustrate the benefits of modernizing methods, including migrating HPLC methods to UHPLC or UPLC, without the need to revalidate.
Topics covered in this webinar will include:
- Pharmacopeial monograph modernization prioritization scheme
- Review of USP General Chapter <621> current allowable adjustments to validated chromatographic methods and forthcoming updates
- Case study on the migration of isocratic and gradient pharmacopeial methods to modern chromatography column technology, highlighting improved method performance and throughput
Replay the webinar, hosted by SelectScience:
https://www.selectscience.net/webinars/pharmacopeial-modernization-how-will-your-chromatography-workflow-benefit/?webinarID=1228
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.
Scared Straight: The Frightening Prospect of Mismanaging a Chemical EmergencyTriumvirate Environmental
This presentation presents the consequences of a mismanaged chemical emergency response to help you better prepare for a possible emergency. Learn about the 5 common missteps and some prevention methods you can implement today.
This presentation provides an overview of the major issues affecting pharmaceutical waste management, insight in to the new rule proposed by the EPA, and what it all means to healthcare facilities and reverse distributors.
This webinar provided methods to reduce waste, spend, and ultimately improve the efficiency of your waste management program. Expert Mike Farrell walked through various disposal options, including solvent recovery, waste to energy, and fuel blending. Attendees learned how to take ownership of their waste program to drive effectiveness and cost control.
This webinar offered insight into world of EH&S technology. Expert speaker, Mike Albert, provided analysis of digital compliance programs and the benefits that can be achieved by making the switch from a paper-only system. He gave an overview of some of the leading software platforms as well as a short demonstration of how Triumvirate's own compliance reporting tool works.
This presentation offers tips and best practices for ensuring your OSHA inspection preparedness. Don't get caught off guard next time OSHA comes knocking. Learn how to prepare your employees and your records in an effort to impress your auditor and minimize the risk of receiving a violation.
This presentation delves into sodium azide uses and health risks, guidelines for storage and handling, and remediation procedures for contaminated waste pipe to ensure a safe work environment. It provides a detailed explanation of NIOSH decontamination procedures and case study examples of sodium azide remediation in action.
How to build a composting program for your institution. Presented by Amy Lipman of Beth Israel Deaconess Medical Center for Triumvirate Environmental's roundtable on the Massachusetts food waste ban.
This presentation introduces an innovative new service provided by Triumvirate Environmental: Red2Green. You will learn about the common issues associated with medical waste disposal today, how the plastic in your RMW can actually be recycled, and what the service adoption and benefits consist of.
THe deadline to convert GHS labeling and the new SDS requirements is fast approaching: June 1, 2015. It's time to understand GHS. This webinar will cover everything you need to know about GHS ompliance. This include:
Written Program and Plan Updates
Labeling with Hazard Warnings and Pictograms
Employee Training Requirements
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.
This presentation outlines the issue of mold in the workplace, offering details on the most common types of mold and how to identify potential sources. It also analyzes your mold danger level and presents recommendations for action and remediation. Learn from a real-world case of mold contamination at a local college.
This presentation provides best practices and tactics for a successful OSHA inspection. It addresses what to expect when OSHA arrives, how to walk Inspectors through your facility and more!
This presentation addresses the various aspects and phases of a stormwater sampling project and how to go about planning and executing your next project. It focuses primarily on the preparation stage and provides tips to help overcome challenges associated with weather forecasts, lab requirements, safety and more.
Pharmaceutical Microbiology: Current and Future Challenges Tim Sandle, Ph.D.
The changing environment for pharmaceutical microbiology
Limitations of methods
Need for new (rapid) methods
Separating people form processes
Single-use technologies
Environmental monitoring programme
Best practices
Rapid methods
Contamination control strategy
Objectionable organisms
Burkholderia cepacia complex
For many higher education institutions, hazardous waste is disposed of as soon as it's generated and waste streams are typically comingled. Unfortunately, this approach toward waste management could cause you to lose money and result in your goals falling flat. It’s time to rethink your approach and adopt a more cost-effective and efficient strategy to managing your hazardous chemical waste.
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.
Do you have contamination in your biology lab? Preventing and remediating contamination in incubators, cold rooms, and biological safety cabinets allows your organization to run a smoother operation, reduce equipment downtime, and create a safe, environmentally compliant and healthy facility. Learn more at https://www.triumvirate.com/field-services/biological-decontamination-services.
Presentation on the importance of planning environmental sampling and some of the data quality issues that can become an issue during a litigation situation. Topics include sampling strategies, documentation, data quality etc.
Passive Samplers for Vapor Intrusion Monitoring: Update of EPA’s Technical S...Chris Lutes
Lutes, C., R. Truesdale, H. Hayes, T. McAlary, H. Dawson, B. Cosky , D. Grossee, B. Schumacher and J. Zimmerman Passive Samplers for Vapor Intrusion Monitoring: Update of EPA’s Technical Support Document and Research Results, Presented at Third International Symposium on Bioremediation and Sustainable Environmental Technologies (Battelle Symposium); Miami Florida 2015
This presentation focuses on tactics for hazardous waste disposal and opportunities to save time and money. It delves into the regulations and how you can take advantage of storage options. Our speaker also addresses waste minimization and ways to reduce and and segregate your waste streams to meet sustainability goals. Learn about a few case studies that back these strategies up.
Single-Use Tangential Flow Filtration for Closed ProcessingMerck Life Sciences
Watch the presentation of this webinar here: https://bit.ly/3b7vD60
Closed processing involves use of physical barriers to separate processing fluid from the external environment. This approach reduces capital expenditures and clean room classification while accelerating time to market. This webinar will present a TFF process run in a closed mode.
Closed processing with single-use technologies is a critical enabler for efficient and robust manufacturing for novel modalities as well as continuous biomanufacturing processing. It can also reduce the dependence on classified clean rooms for traditional modalities. This approach helps to mitigate the risk of contamination by adventitious agents while enhancing operator safety.
In this presentation, we discuss the implementation of closed processing for downstream applications and present the design and performance testing of a single use manufacturing-scale tangential flow filtration system to be able to operate in both functionally and fully closed mode.
In this webinar, you will learn:
• The context of closed processing
• Differences between closed and functionally closed processing
• The drivers for adoption
• Its practical implementation to a TFF step
Single-Use Tangential Flow Filtration for Closed ProcessingMilliporeSigma
Watch the presentation of this webinar here: https://bit.ly/3b7vD60
Closed processing involves use of physical barriers to separate processing fluid from the external environment. This approach reduces capital expenditures and clean room classification while accelerating time to market. This webinar will present a TFF process run in a closed mode.
Closed processing with single-use technologies is a critical enabler for efficient and robust manufacturing for novel modalities as well as continuous biomanufacturing processing. It can also reduce the dependence on classified clean rooms for traditional modalities. This approach helps to mitigate the risk of contamination by adventitious agents while enhancing operator safety.
In this presentation, we discuss the implementation of closed processing for downstream applications and present the design and performance testing of a single use manufacturing-scale tangential flow filtration system to be able to operate in both functionally and fully closed mode.
In this webinar, you will learn:
• The context of closed processing
• Differences between closed and functionally closed processing
• The drivers for adoption
• Its practical implementation to a TFF step
Single use technology: a regulatory perspectiveTGA Australia
An overview of the regulation of single use technology including Good Manufacturing Practice requirements and the types of deficiencies and issues observed at inspections
Similar to VOCLok: A Better Solution for Solvent Waste Collection in Labs (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
OSHA violations are expensive and time consuming to resolve. It is significantly cheaper and easier to create an OSHA-compliant workplace from the start. Ensuring OSHA compliance requires a complete understanding of the OSHA requirements and a complete assessment of your current workplace. In this webinar, our expert will walk you through the key steps to creating an OSHA-compliant workplace.
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
Recently there have been regulatory updates that affect healthcare facilities including standards that apply to hospital accreditation. The Joint Commission applies standards that pertain to federal Medicare and Medicaid reimbursement. Has your facility adapted to comply with the current and updated standards? Hear our expert provide a comprehensive look at the “Environment of Care” and see how to better adapt your facility to ensure the health and safety of hospital staff, patients, and visitors.
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
You have taken the first step and implemented an EHS program in your workplace, but how do you know if the program is working? Do you fall short on meeting department and corporate goals? Do you know which metrics you should be tracking to ensure the success of your EHS program?
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.
Why Audit? What Is the Difference Between Regulatory Auditing and ISO 14001 o...Triumvirate Environmental
We hear about the importance of conducting audits of your facilities. They allow us to be prepared for when the regulators show up. However, have you ever considered obtaining an ISO certification? The two standards that focus solely on EH&S are the ISO 14001 Environmental Management Standard or the ISO 45001 Occupations Health and Safety Standard. This session will cover the importance of auditing, what the ISO standards entail, and how they may actually help you with compliance and to show your end users that you care about your employees' health and safety and the environment.
Managing Medical or Biological Waste in Massachusetts - Guidance for GeneratorsTriumvirate Environmental
Medical or Biological Waste, a.k.a., Regulated Medical Waste, is regulated by the Massachusetts Department of Public Health. DPH has adopted management requirements codified under 105 CMR 480 that affect those who generate such wastes. Individuals impacted by these rules would be employees who are responsible for the medical/bio waste management program and those who manage the waste onsite (e.g., internal transport, storage, onsite treatment, and other handling).
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
Are you prepared for your next OSHA audit? Ensuring OSHA compliance requires a complete understanding of the OSHA requirements and a complete assessment of your current workplace. In this session, Rick will walk you through the key steps to building a compliant EHS program at your worksite and the key performance indicators needed to measure EHS progress.
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.
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Implicitly or explicitly all competing businesses employ a strategy to select a mix
of marketing resources. Formulating such competitive strategies fundamentally
involves recognizing relationships between elements of the marketing mix (e.g.,
price and product quality), as well as assessing competitive and market conditions
(i.e., industry structure in the language of economics).
Premium MEAN Stack Development Solutions for Modern BusinessesSynapseIndia
Stay ahead of the curve with our premium MEAN Stack Development Solutions. Our expert developers utilize MongoDB, Express.js, AngularJS, and Node.js to create modern and responsive web applications. Trust us for cutting-edge solutions that drive your business growth and success.
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Discover the innovative and creative projects that highlight my journey throu...dylandmeas
Discover the innovative and creative projects that highlight my journey through Full Sail University. Below, you’ll find a collection of my work showcasing my skills and expertise in digital marketing, event planning, and media production.
Attending a job Interview for B1 and B2 Englsih learnersErika906060
It is a sample of an interview for a business english class for pre-intermediate and intermediate english students with emphasis on the speking ability.
Falcon stands out as a top-tier P2P Invoice Discounting platform in India, bridging esteemed blue-chip companies and eager investors. Our goal is to transform the investment landscape in India by establishing a comprehensive destination for borrowers and investors with diverse profiles and needs, all while minimizing risk. What sets Falcon apart is the elimination of intermediaries such as commercial banks and depository institutions, allowing investors to enjoy higher yields.
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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.
RMD24 | Debunking the non-endemic revenue myth Marvin Vacquier Droop | First ...BBPMedia1
Marvin neemt je in deze presentatie mee in de voordelen van non-endemic advertising op retail media netwerken. Hij brengt ook de uitdagingen in beeld die de markt op dit moment heeft op het gebied van retail media voor niet-leveranciers.
Retail media wordt gezien als het nieuwe advertising-medium en ook mediabureaus richten massaal retail media-afdelingen op. Merken die niet in de betreffende winkel liggen staan ook nog niet in de rij om op de retail media netwerken te adverteren. Marvin belicht de uitdagingen die er zijn om echt aansluiting te vinden op die markt van non-endemic advertising.
Memorandum Of Association Constitution of Company.pptseri bangash
www.seribangash.com
A Memorandum of Association (MOA) is a legal document that outlines the fundamental principles and objectives upon which a company operates. It serves as the company's charter or constitution and defines the scope of its activities. Here's a detailed note on the MOA:
Contents of Memorandum of Association:
Name Clause: This clause states the name of the company, which should end with words like "Limited" or "Ltd." for a public limited company and "Private Limited" or "Pvt. Ltd." for a private limited company.
https://seribangash.com/article-of-association-is-legal-doc-of-company/
Registered Office Clause: It specifies the location where the company's registered office is situated. This office is where all official communications and notices are sent.
Objective Clause: This clause delineates the main objectives for which the company is formed. It's important to define these objectives clearly, as the company cannot undertake activities beyond those mentioned in this clause.
www.seribangash.com
Liability Clause: It outlines the extent of liability of the company's members. In the case of companies limited by shares, the liability of members is limited to the amount unpaid on their shares. For companies limited by guarantee, members' liability is limited to the amount they undertake to contribute if the company is wound up.
https://seribangash.com/promotors-is-person-conceived-formation-company/
Capital Clause: This clause specifies the authorized capital of the company, i.e., the maximum amount of share capital the company is authorized to issue. It also mentions the division of this capital into shares and their respective nominal value.
Association Clause: It simply states that the subscribers wish to form a company and agree to become members of it, in accordance with the terms of the MOA.
Importance of Memorandum of Association:
Legal Requirement: The MOA is a legal requirement for the formation of a company. It must be filed with the Registrar of Companies during the incorporation process.
Constitutional Document: It serves as the company's constitutional document, defining its scope, powers, and limitations.
Protection of Members: It protects the interests of the company's members by clearly defining the objectives and limiting their liability.
External Communication: It provides clarity to external parties, such as investors, creditors, and regulatory authorities, regarding the company's objectives and powers.
https://seribangash.com/difference-public-and-private-company-law/
Binding Authority: The company and its members are bound by the provisions of the MOA. Any action taken beyond its scope may be considered ultra vires (beyond the powers) of the company and therefore void.
Amendment of MOA:
While the MOA lays down the company's fundamental principles, it is not entirely immutable. It can be amended, but only under specific circumstances and in compliance with legal procedures. Amendments typically require shareholder
What is the TDS Return Filing Due Date for FY 2024-25.pdfseoforlegalpillers
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3. During This Webinar:
All lines will be muted.
Communicate via the questions tab in your
webinar panel.
Unanswered questions will be responded
to after the webinar.
Webinar recording and slides will be
emailed to you tomorrow.
4. Speaker Profile
Ian Lanza
Regional Director of Life
Sciences
He works to add value to companies by improving
sustainability, environmental, and safety performance,
while driving costs down. He works closely with the
world's premiere biotech and pharmaceutical companies
and executive leadership to identify sustainability and
environmental opportunities that can have short-term and
long-term impacts. Ian has been employed by Triumvirate
Environmental for ten years.
5. Agenda
HPLC and Other Laboratory Scale Process & Analytical Machines
Existing Waste Systems
Overview & Benefits of the VOCLok
Implementation and Maintenance
Case Studies
Wrap Up/Q&A
6. HPLC and Other Laboratory
Scale Process & Analytical
Machines
• Many research, development, and process laboratories use
benchtop process machines
• HPLC is the most common process with many applications
• These processes use various types of volatile and hazardous
chemicals to purify or analyze
• After using volatile or hazardous chemicals, the materials are
discharged as a waste
8. Agenda
HPLC and Other Laboratory Scale Process & Analytical Machines
Existing Waste Systems
Overview & Benefits of the VOCLok
Implementation and Maintenance
Case Studies
Wrap Up/Q&A
10. Existing Waste
Collection
Systems
• Process machines do not come with
a waste collection system – the
waste is often an after thought
• When EHS gets involved, more
sophisticated systems can be
employed which vary drastically in
design, regulatory compliance,
ease of use, safety for lab staff,
and cost
11. Common Results
1. Do nothing because compliant systems are too costly or too
complicated to install
• Problems: Dangerous, non-compliant, VOC exposure
2. MacGyver a solution (i.e. drill holes in lids for lines)
• Problems: Non-compliant, VOC exposure
3. Purchase a less expensive, but non-compliant or burdensome
system to manage
• Problems: Limited options, varying levels of compliance, VOC
exposure
4. Buy a highly technical and expensive waste collection system
• Problems: Cost, complicated, limited options
13. Agenda
HPLC and Other Laboratory Scale Process & Analytical Machines
Existing Waste Systems
Overview & Benefits of the VOCLok
Implementation and Maintenance
Case Studies
Wrap Up/Q&A
15. The Design Process
Designed by EHS professionals with compliance, safety,
and flexibility in mind. This resulted in a customizable
set up to fit each process machine and facility’s needs.
The system was designed to be:
• RCRA compliant
• Safe
• Customizable
• Cost competitive
• Elegant
17. • There are currently 12 different containers
• The containers range in size and functionality, from 1 gallon to 55
gallons, from shippable DOT containers to reusable durable containers
• All containers are designed to easily and safely transfer waste into
larger containers
Containers
18. Caps
• Versa Cap System is designed to
easily change waste containers.
The threaded collar allows users
to change containers without
tangling waste lines.
• We utilize many different puck
configurations to match unique
machine waste lines.
• Plugs, hose barbs, tubes, and
grommets come with the cap to
ensure a compliantly and closed
container.
19. Carbon Filters
• Carbon filters grab fugitive and displaced
evaporated solvents and odors from waste container
as waste enters the container
• Filters are outfitted with breakthrough indicators
20. Benefits of the
New System:
Safety
1. Ergonomics
2. The correct container
for the job
3. Capture of rogue
emissions
21. Benefits of the
New System:
Compliance
• Closed waste collection
system results in full RCRA
container closure compliance
• Container sizing can help
reduce hazardous material
volumes in the laboratories
22. Benefits of the
New System: Ease
of Use
• The right container for the job:
• Shippable containers
• Easy to pour containers
• Right sizing the container
• The Versa Cap technology makes it
easy to change out full containers
• Filter system is easy to change
and the breakthrough indicators
ensure filters are changed when
needed
23. Benefits of the
New System:
Cost Savings
• The system was designed and
manufactured to be up to half the
cost of similar setups
• The flexibility in these systems
allows facilities to set up the correct
container for the downstream
management of the waste
• This results in additional cost savings
24. Agenda
HPLC and Other Laboratory Scale Process & Analytical Machines
Existing Waste Systems
Overview & Benefits of the VOCLok
Implementation and Maintenance
Case Studies
Wrap Up/Q&A
25. Pre- Project Planning
• Identify project goal (RCRA
compliance, worker safety,
hazardous material volumes,
hazardous material
management)
• Identify/inventory all
laboratory process machines
• Map out hazardous material
management
• Select containers and caps
26. Scope and
Installation
• Triumvirate staff will scope the
caps and containers needed for
the project
• Triumvirate will supply all of
the caps, containers, and
additional hosing and
connections needed to install
the units
• Certified Triumvirate staff will
install each unit
27. Program
Maintenance
• Maintenance is minimal and can be
rolled into the hazardous waste
SAA compliance program
• Inspect caps and containers for
leaks (SAA RCRA compliance)
• Change filters when they become
loaded
• Utilize the breakthrough indicator
to know when filters need to be
changed
28. Agenda
HPLC and Other Laboratory Scale Process & Analytical Machines
Existing Waste Systems
Overview & Benefits of the VOCLok
Implementation and Maintenance
Case Studies
Wrap Up/Q&A
29. Case Study #1: Managing Flammable
Volumes at a Pharmaceutical Company
• A growing pharmaceutical company in Cambridge, MA was faced
with increasing workers and haz mat levels, while having to reduce
flammable volumes in the laboratories
• EHS was tasked with reducing the flammable volumes stored
throughout the labs
• Through an audit, it was found that there were close to 400 gallons
of flammable waste stored in SAAs throughout the labs
• Triumvirate was asked to design a solution to this problem
30. Case Study #1: Managing Flammable
Volumes at a Pharmaceutical Company
Project Goals:
• Reduce flammable levels in SAAs
by 50%
• Update waste collection system to
ensure RCRA compliance
• Improve safety in the labs
Project Outcomes:
• Installed 75 new waste collection
units throughout the facility
• Reduced flammable levels by 70%
(or 300 gallons)
• The versa cap and filters resulted
in a safer waste collection process
for the waste handlers and lab
workers
31. Case Study #2: Out of Compliance
University
• A large New England university received a notice of non-
compliance from the state environmental regulatory
agency for open containers at the point of generation
• The university was collecting waste from lab scale HPLC
units in various types of waste containers
• The waste lines were fed into open containers
• The University reached out to Triumvirate to provide a
systematic waste collection system for all HPLC machines
32. Project Goals:
• Install a compliant waste
collection system for the
collection of waste from HPLC
• Complete this project within a 5
week time frame
• Complete the project using an
existing waste budget
Project Outcomes:
• Triumvirate installed 34 waste
collection units throughout the
campus in 3 weeks
• The Triumvirate project proposal
was the least expensive and
fastest turnaround
• The University sited the
Triumvirate VOC Lok system in the
response letter to the notice of
non-compliance
Case Study #2: Out of Compliance
University
33. Agenda
HPLC and Other Laboratory Scale Process & Analytical Machines
Existing Waste Systems
Overview & Benefits of the VOCLok
Implementation and Maintenance
Case Studies
Wrap Up/Q&A
34. Wrap Up
Existing waste collection systems are flawed
The VOCLok addresses limitations and allows for
maximum
compliance and cost savings
Implementation is customized to fit user
requirements
Maintenance is minimal and managed by Triumvirate
36. Thank You For
Attending!
Ensure that your solvent waste
collection process is compliant:
http://info.triumvirate.com/free-
consultation-voclok
Call Us!
1-888-834-9697
www.triumvirate.com
Contact Ian:
ilanza@triumvirate.com
617-715-9002