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This document outlines the policies, requirements, and activities of an environmental lab for monitoring and compliance. It includes inputs from various departments on vision, safety, social responsibility, and maintenance policies. The lab establishes monitoring programs for air, water, noise and other areas according to legal requirements for establishment, operation and renewal. It monitors pollution control devices, ambient and stack emissions, bacteriology, and conducts audits. The lab aims to meet compliance standards through management programs and addressing any non-conformances found in monitoring results.
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Ciao,
Riccardo
Leveraging Gap Assessments and Internal Audits in ISO 22301
A focus on the strategic operation of the assessment and audit function of the BCMS to meet system goals and objectives, maintain conformance and leverage to enhance the awareness and benefits of the BCMS. Topics include the design and methodology of the internal audit plan and opportunities for using proven performance to promote awareness of the BCMS and quantify value of the system.
Main points covered:
• Gap Assessment and Internal Audit Plan
• Methodology
• Show ROI on performance
Presenter:
The presenter of this webinar will be Jan Decker. She is a Consultant in Emergency Management, Crisis Management and related Business Continuity plans, programs, and information systems. She is certified ISO 22301 Lead Implementer and Lead Auditor Trainer.
Link of the recorded session published on YouTube: https://youtu.be/7AyikpO6GLA
Corporate Social Responsibility: Balancing the Risks and Rewards
Geary Sikich is the principal of Logical Management Systems Corp., a consulting firm focused on enterprise risk management and issues analysis. Prior to founding Logical Management Systems in 1985, Geary held senior operational positions in various industries. The document contains information about Geary Sikich and his company, including contact details, and discusses various topics related to corporate social responsibility, risk management, and strategic planning. It provides copyright information and contains multiple sections related to these topics.
Embed RBI in your EAM
This document discusses embedding Risk-Based Inspection (RBI) software within IBM Maximo enterprise asset management solutions. RBI helps asset-intensive industries improve safety, uptime, and cost control by predicting failures and focusing resources. Embedding RBI provides predictive models, reliability analysis, and compliance monitoring to maximize asset performance while leveraging existing EAM investments. It can quantify risk, predict failures, focus work, and enable continuous improvement through an integrated approach within the Maximo platform.
[Kho tài liệu ngành may] tiếng anh chuyên ngành may
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Huawei RET alarms Troubleshooting Guide Flow Chart
Flow Chart describes RET Alarms Troubleshooting in Huawei Node-B
* ALM-26751 RET Antenna Motor Fault
* ALM-26752 ALD Hardware Fault
* ALM-26754 RET Antenna Data Loss
* ALM-26753 RET Antenna Not Calibrated
* ALM-26541 ALD Maintenance Link Failure
* ALM-26530 RF Unit ALD Current Out of Range
* ALM-26531 RF Unit ALD Switch Configuration Mismatch
* ALM-26757 RET Antenna Running Data and Configuration Mismatch
We've been hacked! Now, what's the BCP?
In this webinar, we will discuss how to Integrate Information Security with Business Continuity Planning. Tips for reducing BCP volumes and preventing your plan from ‘collecting dust on the shelf’ and achieving a hands-on BCP process and getting your organization truly 'incident ready'.
Main points covered:
• Integrating Information Security with Business Continuity Planning (BCP)
• Tips for reducing BCP volumes and preventing your plan from 'collecting dust on the shelf'
• Achieving a hands-on BCP process and getting your organization truly 'incident ready'
Presenter:
The presenter of this webinar will be Ms. Rinske Geerlings MSc, CBCP, MBCI, COBIT, ISO 22301 Master, ISO 31000 Lead Risk Manager, ISO 27001 Lead Implementer, and ITIL Master. She is an internationally known, award-winning consultant, speaker and certified trainer in Business Continuity, IT Management, Disaster Recovery, Risk Management and Information Security with 20 years global experience.
Link of the recorded session published on YouTube: https://youtu.be/5_lnQyFlGTs
Mori Seiki Maintenance Guide
This is a complete guide to all the inspection procedures you have to perform to the Mori Seiki machine.
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How to improve resilience and respond better to Cyber Attacks with ISO 22301?
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Leveraging Gap Assessments and Internal Audits in ISO 22301
Leveraging Gap Assessments and Internal Audits in ISO 22301
Corporate Social Responsibility: Balancing the Risks and Rewards
Corporate Social Responsibility: Balancing the Risks and Rewards
[Kho tài liệu ngành may] tiếng anh chuyên ngành may
[Kho tài liệu ngành may] tiếng anh chuyên ngành may
Huawei RET alarms Troubleshooting Guide Flow Chart
Huawei RET alarms Troubleshooting Guide Flow Chart
Similar to Process-flow CHART.
GOOD LABORATORY PRACTICES
Good laboratory practices (GLP) were established in the 1970s after fraudulent data was submitted to the FDA from toxicology laboratories. The key case involved Industrial Bio-Test Laboratories, which falsified safety tests. This led the FDA to create GLP regulations in 1978 to ensure non-clinical study data quality and integrity. The OECD later established universal GLP principles in 1981 to facilitate international acceptance of study data. GLP provides standards for test facility organization and quality management, facilities, test system handling, study conduct, reporting, and record keeping to ensure study data accurately represent results. India has established a National GLP Compliance Monitoring Authority to oversee adherence to GLP standards by domestic testing facilities.
Glp ppt
GLP (Good Laboratory Practice) is a quality system concerned with the organization and conditions under which non-clinical health and environmental safety studies are conducted. It was instituted in the US after fraudulent data was submitted by toxicology labs to the FDA. The OECD then established principles of GLP to harmonize standards internationally. The key principles cover organization and personnel, quality assurance, facilities, equipment, test systems, study conduct, reporting and record keeping. Compliance ensures the validity and integrity of study data submitted to regulatory authorities like the FDA. India has a National GLP Compliance Monitoring Authority that inspects and certifies laboratories according to OECD GLP principles.
Glp
The document discusses Good Laboratory Practices (GLP), which are regulations created by the FDA in 1978 that provide a framework for conducting laboratory studies. GLP was established in response to cases of poor laboratory practices including fraudulent activities and inaccurate reporting of results. The objectives of GLP are to ensure data submitted accurately reflects study results and is traceable. Laboratories must comply with standards for facilities, equipment, record-keeping, personnel qualifications and quality control to avoid penalties for noncompliance like disqualification and inability to conduct future studies.
Glp
The document discusses Good Laboratory Practices (GLP), which are regulations created by the FDA in 1978 that provide a framework for conducting laboratory studies. GLP was established in response to cases of poor laboratory practices including fraudulent activities and inaccurate reporting of results. The objectives of GLP are to ensure data submitted accurately reflects study results and is traceable. Laboratories must comply with requirements around facilities, equipment, recordkeeping, personnel qualifications and standard operating procedures to adhere to GLP. Noncompliance can result in disqualification and civil or criminal penalties for the laboratory.
GLP.ppt
Good Laboratory Practices (GLP) are regulations created by the FDA in 1978 that provide a framework for conducting laboratory studies. GLP aims to ensure study data accurately reflects results and is traceable. The regulations were established in response to discovered fraudulent activities and poor practices in toxicology labs in the 1970s. Facilities that do not comply with GLP standards risk disqualification, meaning they cannot conduct new studies or submit existing ones. Disqualified facilities can apply for reinstatement by demonstrating they will adhere to GLP procedures going forward.
GLP.ppt
Good Laboratory Practices (GLP) are regulations created by the FDA in 1978 that provide a framework for conducting laboratory studies. GLP aims to ensure study data accurately reflects results and is traceable. The regulations were established in response to discovered fraudulent activities and poor practices at toxicology labs in the 1970s. Facilities that do not comply with GLP standards risk disqualification, meaning they cannot conduct new studies or submit existing ones. Disqualified facilities can apply for reinstatement by demonstrating they will adhere to GLP procedures going forward.
Glp
GLP refers to Good Laboratory Practice, which are standards set by the FDA for conducting laboratory studies. GLP was created in the late 1970s after investigations found many cases of fraudulent activities and poor practices in toxicology labs. The objectives of GLP are to ensure laboratory data accurately reflects study results and is traceable. Facilities that do not comply with GLP standards risk disqualification, meaning they cannot conduct or submit studies to the FDA. Disqualification can occur if noncompliance affected study validity or a facility failed to improve after warnings.
Good Laboratory Practice
GLP (Good Laboratory Practice) is a quality system concerned with conducting non-clinical safety studies. It aims to ensure studies are accurately reported and not fraudulent. GLP has principles for organization, personnel, facilities, test systems, operating procedures, performance and reporting of studies. India's National GLP Compliance Monitoring Authority monitors adherence. GLP compliance certification is required for safety studies of products like pesticides, pharmaceuticals and food additives, and helps protect human and environmental health while facilitating international trade.
Glp
The document discusses the history and purpose of Good Laboratory Practice (GLP). It begins by explaining that GLP originated in the United States in the 1970s when the FDA found many cases of poor laboratory practices. The FDA then created GLP regulations in 1978 to promote quality and validity in non-clinical lab studies. The Organization for Economic Co-operation and Development (OECD) later established widely accepted GLP principles based on the US regulations. GLP aims to minimize mistakes and ensure consistency, documentation, and reproducibility in lab studies submitted to regulatory authorities. The document then goes on to discuss key aspects of GLP such as management responsibilities, quality assurance programs, standard operating procedures, and record keeping.
Good laboratory practices (GLP)
Good laboratory practices
introduction
reasons behind the creation of glp
Objectives of GLP
The OECD
GLP principles
Test facility organizational and personnel
Quality assurance programme
Facilities
Apparatus, materials and reagents
Test systems
Test and reference items
SOPS- Standard Operating Procedures
Performance of the study
Reporting of the study details
Storage and retention of records and materials
What GLP must contain?
Do this for GLP
Benefits of GLP
Conclusion
Good laboratory practices
Good Laboratory Practice (GLP) regulations were created by the FDA in the 1970s after discovering fraudulent activities and poor lab practices that undermined the quality and integrity of data submitted to the FDA. GLP aims to ensure that studies are conducted properly according to standardized operating procedures and that accurate records are kept. This allows data from non-clinical studies to be reliably submitted to regulatory authorities. Key aspects of GLP include requirements for facilities, test systems, operating procedures, personnel qualifications, quality assurance programs, and record keeping. Following GLP helps assure reproducibility and quality of results.
Good Laboratory Practice (GLP)
This document provides an overview of Good Laboratory Practices (GLP). It states that GLP is an FDA regulation that establishes a framework for conducting laboratory studies. The document discusses the history of GLP, including how it originated in the US in 1978 in response to cases of poor laboratory practices. It describes the objectives and mission of GLP to ensure data integrity and traceability. Key aspects of GLP like standard operating procedures, record keeping, and facility certification are summarized. Consequences of noncompliance, such as disqualification and inability to conduct studies, are also outlined.
Introduction to good laboratory practices
Good Laborarory Practices. Good Laboratory Practices (GLP) covers the organizational process and conditions under which clinical field studies are conducted, monitored, recorded and reported. GLP is carried out to improve quality of data for its international acceptance.
GOOD LABORATORY PRACTICES
GLP (Good Laboratory Practice) is a quality system for non-clinical health and environmental safety studies. It was instituted in the US after fraudulent data was submitted by toxicology labs. GLP aims to ensure studies are properly planned, monitored, and reported, and that data accurately reflects results. It promotes international acceptance of safety tests. The OECD principles provide an international standard for GLP, covering topics like facility organization, test system and item characterization, and record keeping. India has established a National GLP Compliance Monitoring Authority to oversee GLP standards.
Good laboratory practices (GLP) himanshu
Good Laboratory Practices (GLP)
History
Reason behind GLP created
Advantages and disadvantages of GLP
Objectives of GLP
Practice of GLP
b pharma 6th sem
pharmaceutical quality assurance
Glp
GLP (Good Laboratory Practice) is a quality system with defined standards for conducting studies and reporting results. It ensures uniformity, consistency, reliability and reproducibility of testing through elements like SOPs, personnel roles, equipment validation and laboratory safety practices. Key aspects of GLP include establishing an independent quality assurance unit, documenting all study activities, ensuring personnel are qualified and equipment is properly maintained and calibrated, and archiving records for a defined period of time. Following GLP helps provide reasonable assurance that study results were collected as outlined and can be relied upon, even if it does not guarantee the scientific merit of the study itself.
Good laboratory practices
The document discusses Good Laboratory Practices (GLP) which provide a framework for conducting laboratory studies on chemicals and pharmaceuticals. It outlines that GLP were established to ensure quality, consistency and integrity of safety testing. The key points covered include:
- GLP applies to nonclinical safety studies for chemicals and pharmaceuticals
- They help assure regulators that submitted data accurately reflects study results
- Major events leading to their creation in response to fraud and misconduct in some laboratories
Good Laboratory Practices Mubashir Maqbool
GLP (Good Laboratory Practice) is a quality system for managing non-clinical laboratory studies to ensure reliability and integrity of test data. It outlines requirements for facility organization, personnel responsibilities, quality assurance programs, standard operating procedures, and retention of records and reports. GLP aims to ensure studies are well-designed, conducted and documented according to all principles to allow for traceability and reproducibility of results.
Good laboratoty practise
Good Laboratory Practices: General Provisions, Organization and Personnel, Facilities, Equipment,
Testing Facilities Operation, Test and Control Articles, Protocol for Conduct of a Nonclinical Laboratory
Study, Records and Reports, Disqualification of Testing Facilities, Organization and Personnel, Facilities, Equipment,
Testing Facilities Operation, Test and Control Articles, Protocol for Conduct of a Nonclinical Laboratory
Study, Records and Reports, Disqualification of Testing Facilities
Glp seminar
The document discusses the MOD, which is an abbreviation that stands for Ministry of Defence in the United Kingdom. The MOD is responsible for implementing the defence policy set by Her Majesty's Government and the defence of the UK and overseas territories. It is the largest government department, employing over 100,000 full-time personnel and is responsible for defence policy, procurement, and the Armed Forces of the UK.
Similar to Process-flow CHART. (20)
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The incorporation of a 3DCSM and completion of HRSC provided a tool for enhanced, data-driven, decisions to support a change in remediation closure strategies. Currently, an approved pilot study has been obtained to shut-down the remediation systems (ISCO, P&T) and conduct a hydraulic study under non-pumping conditions. A separate micro-biological bench scale treatability study was competed that yielded positive results for an emerging innovative technology. As a result, a field pilot study has commenced with results expected in nine-twelve months. With the results of the hydraulic study, field pilot studies and an updated risk assessment leading site monitoring optimization cost lifecycle savings upwards of $15MM towards an alternatively evolved best available technology remediation closure strategy.
一比一原版西澳大学毕业证学历证书如何办理
原版定制【微信:741003700】《西澳大学毕业证学位证成绩单》【微信:741003700】成绩单 、雅思、外壳、留信学历认证永久存档查询，采用学校原版纸张、特殊工艺完全按照原版一比一制作（包括：隐形水印，阴影底纹，钢印LOGO烫金烫银，LOGO烫金烫银复合重叠，文字图案浮雕，激光镭射，紫外荧光，温感，复印防伪）行业标杆！精益求精，诚心合作，真诚制作！多年品质 ,按需精细制作，24小时接单,全套进口原装设备，十五年致力于帮助留学生解决难题，业务范围有加拿大、英国、澳洲、韩国、美国、新加坡，新西兰等学历材料，包您满意。
【业务选择办理准则】
一、工作未确定，回国需先给父母、亲戚朋友看下文凭的情况，办理一份毕业证【Q微信741003700】文凭即可
二、回国进私企、外企、自己做生意的情况，这些单位是不查询毕业证真伪的，而且国内没有渠道去查询国外文凭的真假，也不需要提供真实教育部认证。鉴于此，办理一份毕业证【Q微信741003700】即可
三、进国企，银行，事业单位，考公务员等等，这些单位是必需要提供真实教育部认证的，办理教育部认证所需资料众多且烦琐，所有材料您都必须提供原件，我们凭借丰富的经验，快捷的绿色通道帮您快速整合材料，让您少走弯路。
留信网认证的作用:
1:该专业认证可证明留学生真实身份
2:同时对留学生所学专业登记给予评定
3:国家专业人才认证中心颁发入库证书
4:这个认证书并且可以归档倒地方
5:凡事获得留信网入网的信息将会逐步更新到个人身份内，将在公安局网内查询个人身份证信息后，同步读取人才网入库信息
6:个人职称评审加20分
7:个人信誉贷款加10分
8:在国家人才网主办的国家网络招聘大会中纳入资料，供国家高端企业选择人才
【关于价格问题（保证一手价格）】
我们所定的价格是非常合理的，而且我们现在做得单子大多数都是代理和回头客户介绍的所以一般现在有新的单子 我给客户的都是第一手的代理价格，因为我想坦诚对待大家 不想跟大家在价格方面浪费时间
对于老客户或者被老客户介绍过来的朋友，我们都会适当给一些优惠。
原版制作(Newcastle毕业证书)纽卡斯尔大学毕业证在读证明一模一样
学校原件一模一样【微信：741003700 】《(Newcastle毕业证书)纽卡斯尔大学毕业证》【微信：741003700 】学位证，留信认证（真实可查，永久存档）原件一模一样纸张工艺/offer、雅思、外壳等材料/诚信可靠,可直接看成品样本，帮您解决无法毕业带来的各种难题！外壳，原版制作，诚信可靠，可直接看成品样本。行业标杆！精益求精，诚心合作，真诚制作！多年品质 ,按需精细制作，24小时接单,全套进口原装设备。十五年致力于帮助留学生解决难题，包您满意。
本公司拥有海外各大学样板无数，能完美还原。
1:1完美还原海外各大学毕业材料上的工艺：水印，阴影底纹，钢印LOGO烫金烫银，LOGO烫金烫银复合重叠。文字图案浮雕、激光镭射、紫外荧光、温感、复印防伪等防伪工艺。材料咨询办理、认证咨询办理请加学历顾问Q/微741003700
【主营项目】
一.毕业证【q微741003700】成绩单、使馆认证、教育部认证、雅思托福成绩单、学生卡等！
二.真实使馆公证(即留学回国人员证明,不成功不收费)
三.真实教育部学历学位认证（教育部存档！教育部留服网站永久可查）
四.办理各国各大学文凭(一对一专业服务,可全程监控跟踪进度)
如果您处于以下几种情况：
◇在校期间，因各种原因未能顺利毕业……拿不到官方毕业证【q/微741003700】
◇面对父母的压力，希望尽快拿到；
◇不清楚认证流程以及材料该如何准备；
◇回国时间很长，忘记办理；
◇回国马上就要找工作，办给用人单位看；
◇企事业单位必须要求办理的
◇需要报考公务员、购买免税车、落转户口
◇申请留学生创业基金
留信网认证的作用:
1:该专业认证可证明留学生真实身份
2:同时对留学生所学专业登记给予评定
3:国家专业人才认证中心颁发入库证书
4:这个认证书并且可以归档倒地方
5:凡事获得留信网入网的信息将会逐步更新到个人身份内，将在公安局网内查询个人身份证信息后，同步读取人才网入库信息
6:个人职称评审加20分
7:个人信誉贷款加10分
8:在国家人才网主办的国家网络招聘大会中纳入资料，供国家高端企业选择人才
在线办理(lboro毕业证书)拉夫堡大学毕业证学历证书一模一样
学校原件一模一样【微信：741003700 】《(lboro毕业证书)拉夫堡大学毕业证学历证书》【微信：741003700 】学位证，留信认证（真实可查，永久存档）原件一模一样纸张工艺/offer、雅思、外壳等材料/诚信可靠,可直接看成品样本，帮您解决无法毕业带来的各种难题！外壳，原版制作，诚信可靠，可直接看成品样本。行业标杆！精益求精，诚心合作，真诚制作！多年品质 ,按需精细制作，24小时接单,全套进口原装设备。十五年致力于帮助留学生解决难题，包您满意。
本公司拥有海外各大学样板无数，能完美还原。
1:1完美还原海外各大学毕业材料上的工艺：水印，阴影底纹，钢印LOGO烫金烫银，LOGO烫金烫银复合重叠。文字图案浮雕、激光镭射、紫外荧光、温感、复印防伪等防伪工艺。材料咨询办理、认证咨询办理请加学历顾问Q/微741003700
【主营项目】
一.毕业证【q微741003700】成绩单、使馆认证、教育部认证、雅思托福成绩单、学生卡等！
二.真实使馆公证(即留学回国人员证明,不成功不收费)
三.真实教育部学历学位认证（教育部存档！教育部留服网站永久可查）
四.办理各国各大学文凭(一对一专业服务,可全程监控跟踪进度)
如果您处于以下几种情况：
◇在校期间，因各种原因未能顺利毕业……拿不到官方毕业证【q/微741003700】
◇面对父母的压力，希望尽快拿到；
◇不清楚认证流程以及材料该如何准备；
◇回国时间很长，忘记办理；
◇回国马上就要找工作，办给用人单位看；
◇企事业单位必须要求办理的
◇需要报考公务员、购买免税车、落转户口
◇申请留学生创业基金
留信网认证的作用:
1:该专业认证可证明留学生真实身份
2:同时对留学生所学专业登记给予评定
3:国家专业人才认证中心颁发入库证书
4:这个认证书并且可以归档倒地方
5:凡事获得留信网入网的信息将会逐步更新到个人身份内，将在公安局网内查询个人身份证信息后，同步读取人才网入库信息
6:个人职称评审加20分
7:个人信誉贷款加10分
8:在国家人才网主办的国家网络招聘大会中纳入资料，供国家高端企业选择人才
Optimizing Post Remediation Groundwater Performance with Enhanced Microbiolog...
Results of geophysics and pneumatic injection pilot tests during 2003 – 2007 yielded significant positive results for injection delivery design and contaminant mass treatment, resulting in permanent shut-down of an existing groundwater Pump & Treat system.
Accessible source areas were subsequently removed (2011) by soil excavation and treated with the placement of Emulsified Vegetable Oil EVO and zero-valent iron ZVI to accelerate treatment of impacted groundwater in overburden and weathered fractured bedrock. Post pilot test and post remediation groundwater monitoring has included analyses of CVOCs, organic fatty acids, dissolved gases and QuantArray® -Chlor to quantify key microorganisms (e.g., Dehalococcoides, Dehalobacter, etc.) and functional genes (e.g., vinyl chloride reductase, methane monooxygenase, etc.) to assess potential for reductive dechlorination and aerobic cometabolism of CVOCs.
In 2022, the first commercial application of MetaArray™ was performed at the site. MetaArray™ utilizes statistical analysis, such as principal component analysis and multivariate analysis to provide evidence that reductive dechlorination is active or even that it is slowing. This creates actionable data allowing users to save money by making important site management decisions earlier.
The results of the MetaArray™ analysis’ support vector machine (SVM) identified groundwater monitoring wells with a 80% confidence that were characterized as either Limited for Reductive Decholorination or had a High Reductive Reduction Dechlorination potential. The results of MetaArray™ will be used to further optimize the site’s post remediation monitoring program for monitored natural attenuation.
快速办理(Calabria毕业证书)卡拉布里亚大学毕业证在读证明一模一样
原件一模一样【微信：bwp0011】《(Calabria毕业证书)卡拉布里亚大学毕业证》【微信：bwp0011】学位证，留信认证（真实可查，永久存档）原件一模一样纸张工艺/offer、雅思、外壳等材料/诚信可靠,可直接看成品样本，帮您解决无法毕业带来的各种难题！外壳，原版制作，诚信可靠，可直接看成品样本。行业标杆！精益求精，诚心合作，真诚制作！多年品质 ,按需精细制作，24小时接单,全套进口原装设备。十五年致力于帮助留学生解决难题，包您满意。
本公司拥有海外各大学样板无数，能完美还原。
1:1完美还原海外各大学毕业材料上的工艺：水印，阴影底纹，钢印LOGO烫金烫银，LOGO烫金烫银复合重叠。文字图案浮雕、激光镭射、紫外荧光、温感、复印防伪等防伪工艺。材料咨询办理、认证咨询办理请加学历顾问微bwp0011
【主营项目】
一.毕业证【微bwp0011】成绩单、使馆认证、教育部认证、雅思托福成绩单、学生卡等！
二.真实使馆公证(即留学回国人员证明,不成功不收费)
三.真实教育部学历学位认证（教育部存档！教育部留服网站永久可查）
四.办理各国各大学文凭(一对一专业服务,可全程监控跟踪进度)
如果您处于以下几种情况：
◇在校期间，因各种原因未能顺利毕业……拿不到官方毕业证【微bwp0011】
◇面对父母的压力，希望尽快拿到；
◇不清楚认证流程以及材料该如何准备；
◇回国时间很长，忘记办理；
◇回国马上就要找工作，办给用人单位看；
◇企事业单位必须要求办理的
◇需要报考公务员、购买免税车、落转户口
◇申请留学生创业基金
留信网认证的作用:
1:该专业认证可证明留学生真实身份
2:同时对留学生所学专业登记给予评定
3:国家专业人才认证中心颁发入库证书
4:这个认证书并且可以归档倒地方
5:凡事获得留信网入网的信息将会逐步更新到个人身份内，将在公安局网内查询个人身份证信息后，同步读取人才网入库信息
6:个人职称评审加20分
7:个人信誉贷款加10分
8:在国家人才网主办的国家网络招聘大会中纳入资料，供国家高端企业选择人才
学校原版(unuk学位证书)英国牛津布鲁克斯大学毕业证硕士文凭原版一模一样
原版定制【微信:bwp0011】《(unuk学位证书)英国牛津布鲁克斯大学毕业证硕士文凭》【微信:bwp0011】成绩单 、雅思、外壳、留信学历认证永久存档查询，采用学校原版纸张、特殊工艺完全按照原版一比一制作（包括：隐形水印，阴影底纹，钢印LOGO烫金烫银，LOGO烫金烫银复合重叠，文字图案浮雕，激光镭射，紫外荧光，温感，复印防伪）行业标杆！精益求精，诚心合作，真诚制作！多年品质 ,按需精细制作，24小时接单,全套进口原装设备，十五年致力于帮助留学生解决难题，业务范围有加拿大、英国、澳洲、韩国、美国、新加坡，新西兰等学历材料，包您满意。
【业务选择办理准则】
一、工作未确定，回国需先给父母、亲戚朋友看下文凭的情况，办理一份就读学校的毕业证【微信bwp0011】文凭即可
二、回国进私企、外企、自己做生意的情况，这些单位是不查询毕业证真伪的，而且国内没有渠道去查询国外文凭的真假，也不需要提供真实教育部认证。鉴于此，办理一份毕业证【微信bwp0011】即可
三、进国企，银行，事业单位，考公务员等等，这些单位是必需要提供真实教育部认证的，办理教育部认证所需资料众多且烦琐，所有材料您都必须提供原件，我们凭借丰富的经验，快捷的绿色通道帮您快速整合材料，让您少走弯路。
留信网认证的作用:
1:该专业认证可证明留学生真实身份
2:同时对留学生所学专业登记给予评定
3:国家专业人才认证中心颁发入库证书
4:这个认证书并且可以归档倒地方
5:凡事获得留信网入网的信息将会逐步更新到个人身份内，将在公安局网内查询个人身份证信息后，同步读取人才网入库信息
6:个人职称评审加20分
7:个人信誉贷款加10分
8:在国家人才网主办的国家网络招聘大会中纳入资料，供国家高端企业选择人才
【关于价格问题（保证一手价格）】
我们所定的价格是非常合理的，而且我们现在做得单子大多数都是代理和回头客户介绍的所以一般现在有新的单子 我给客户的都是第一手的代理价格，因为我想坦诚对待大家 不想跟大家在价格方面浪费时间
对于老客户或者被老客户介绍过来的朋友，我们都会适当给一些优惠。
原版制作(Manitoba毕业证书)曼尼托巴大学毕业证学位证一模一样
学校原件一模一样【微信：741003700 】《(Manitoba毕业证书)曼尼托巴大学毕业证学位证》【微信：741003700 】学位证，留信认证（真实可查，永久存档）原件一模一样纸张工艺/offer、雅思、外壳等材料/诚信可靠,可直接看成品样本，帮您解决无法毕业带来的各种难题！外壳，原版制作，诚信可靠，可直接看成品样本。行业标杆！精益求精，诚心合作，真诚制作！多年品质 ,按需精细制作，24小时接单,全套进口原装设备。十五年致力于帮助留学生解决难题，包您满意。
本公司拥有海外各大学样板无数，能完美还原。
1:1完美还原海外各大学毕业材料上的工艺：水印，阴影底纹，钢印LOGO烫金烫银，LOGO烫金烫银复合重叠。文字图案浮雕、激光镭射、紫外荧光、温感、复印防伪等防伪工艺。材料咨询办理、认证咨询办理请加学历顾问Q/微741003700
【主营项目】
一.毕业证【q微741003700】成绩单、使馆认证、教育部认证、雅思托福成绩单、学生卡等！
二.真实使馆公证(即留学回国人员证明,不成功不收费)
三.真实教育部学历学位认证（教育部存档！教育部留服网站永久可查）
四.办理各国各大学文凭(一对一专业服务,可全程监控跟踪进度)
如果您处于以下几种情况：
◇在校期间，因各种原因未能顺利毕业……拿不到官方毕业证【q/微741003700】
◇面对父母的压力，希望尽快拿到；
◇不清楚认证流程以及材料该如何准备；
◇回国时间很长，忘记办理；
◇回国马上就要找工作，办给用人单位看；
◇企事业单位必须要求办理的
◇需要报考公务员、购买免税车、落转户口
◇申请留学生创业基金
留信网认证的作用:
1:该专业认证可证明留学生真实身份
2:同时对留学生所学专业登记给予评定
3:国家专业人才认证中心颁发入库证书
4:这个认证书并且可以归档倒地方
5:凡事获得留信网入网的信息将会逐步更新到个人身份内，将在公安局网内查询个人身份证信息后，同步读取人才网入库信息
6:个人职称评审加20分
7:个人信誉贷款加10分
8:在国家人才网主办的国家网络招聘大会中纳入资料，供国家高端企业选择人才
Kinetic studies on malachite green dye adsorption from aqueous solutions by A...
Kinetic studies on malachite green dye adsorption from aqueous solutions by A...Open Access Research Paper
Water polluted by dyestuffs compounds is a global threat to health and the environment; accordingly, we prepared a green novel sorbent chemical and Physical system from an algae, chitosan and chitosan nanoparticle and impregnated with algae with chitosan nanocomposite for the sorption of Malachite green dye from water. The algae with chitosan nanocomposite by a simple method and used as a recyclable and effective adsorbent for the removal of malachite green dye from aqueous solutions. Algae, chitosan, chitosan nanoparticle and algae with chitosan nanocomposite were characterized using different physicochemical methods. The functional groups and chemical compounds found in algae, chitosan, chitosan algae, chitosan nanoparticle, and chitosan nanoparticle with algae were identified using FTIR, SEM, and TGADTA/DTG techniques. The optimal adsorption conditions, different dosages, pH and Temperature the amount of algae with chitosan nanocomposite were determined. At optimized conditions and the batch equilibrium studies more than 99% of the dye was removed. The adsorption process data matched well kinetics showed that the reaction order for dye varied with pseudo-first order and pseudo-second order. Furthermore, the maximum adsorption capacity of the algae with chitosan nanocomposite toward malachite green dye reached as high as 15.5mg/g, respectively. Finally, multiple times reusing of algae with chitosan nanocomposite and removing dye from a real wastewater has made it a promising and attractive option for further practical applications.
Biomimicry in agriculture: Nature-Inspired Solutions for a Greener Future
Presentation made for the Webinar Series on Biomimicry for sustainability on 1st June 2024 organized by Green Building Council Sri Lanka
Lessons from operationalizing integrated landscape approaches
Presented by James Reed at "9th Landscape Sustainability Science Forum" on 11 May 2024
Environment Conservation Rules 2023 (ECR)-2023.pptx
Bangladesh Environment Conservation Rules 2023 (ECR-2023).
按照学校原版(UAL文凭证书)伦敦艺术大学毕业证快速办理
挂科购买【(UAL毕业证书)伦敦艺术大学毕业证】【176555708微信号】留学假毕业证成绩单、外壳、offer、留信学历认证（永久存档真实可查）采用学校原版纸张、特殊工艺完全按照原版一比一制作（包括：隐形水印，阴影底纹，钢印LOGO烫金烫银，LOGO烫金烫银复合重叠，文字图案浮雕，激光镭射，紫外荧光，温感，复印防伪）行业标杆！精益求精，诚心合作，真诚制作！多年品质 ,按需精细制作，24小时接单,全套进口原装设备，十五年致力于帮助留学生解决难题，业务范围有加拿大、英国、澳洲、韩国、美国、新加坡，新西兰等学历材料，包您满意。
【我们承诺采用的是学校原版纸张（纸质、底色、纹路），我们拥有全套进口原装设备，特殊工艺都是采用不同机器制作，仿真度基本可以达到100%，所有工艺效果都可提前给客户展示，不满意可以根据客户要求进行调整，直到满意为止！】
【业务选择办理准则】
一、工作未确定，回国需先给父母、亲戚朋友看下文凭的情况，办理一份就读学校的毕业证【微信176555708】文凭即可
二、回国进私企、外企、自己做生意的情况，这些单位是不查询毕业证真伪的，而且国内没有渠道去查询国外文凭的真假，也不需要提供真实教育部认证。鉴于此，办理一份毕业证【微信176555708】即可
三、进国企，银行，事业单位，考公务员等等，这些单位是必需要提供真实教育部认证的，办理教育部认证所需资料众多且烦琐，所有材料您都必须提供原件，我们凭借丰富的经验，快捷的绿色通道帮您快速整合材料，让您少走弯路。
留信网认证的作用:
1:该专业认证可证明留学生真实身份
2:同时对留学生所学专业登记给予评定
3:国家专业人才认证中心颁发入库证书
4:这个认证书并且可以归档倒地方
5:凡事获得留信网入网的信息将会逐步更新到个人身份内，将在公安局网内查询个人身份证信息后，同步读取人才网入库信息
6:个人职称评审加20分
7:个人信誉贷款加10分
8:在国家人才网主办的国家网络招聘大会中纳入资料，供国家高端企业选择人才
留信网服务项目：
1、留学生专业人才库服务（留信分析）
2、国（境）学习人员提供就业推荐信服务
3、留学人员区块链存储服务
→ 【关于价格问题（保证一手价格）】
我们所定的价格是非常合理的，而且我们现在做得单子大多数都是代理和回头客户介绍的所以一般现在有新的单子 我给客户的都是第一手的代理价格，因为我想坦诚对待大家 不想跟大家在价格方面浪费时间
对于老客户或者被老客户介绍过来的朋友，我们都会适当给一些优惠。
选择实体注册公司办理，更放心，更安全！我们的承诺：客户在留信官方认证查询网站查询到认证通过结果后付款，不成功不收费！
Improving the viability of probiotics by encapsulation methods for developmen...
Improving the viability of probiotics by encapsulation methods for developmen...Open Access Research Paper
The popularity of functional foods among scientists and common people has been increasing day by day. Awareness and modernization make the consumer think better regarding food and nutrition. Now a day’s individual knows very well about the relation between food consumption and disease prevalence. Humans have a diversity of microbes in the gut that together form the gut microflora. Probiotics are the health-promoting live microbial cells improve host health through gut and brain connection and fighting against harmful bacteria. Bifidobacterium and Lactobacillus are the two bacterial genera which are considered to be probiotic. These good bacteria are facing challenges of viability. There are so many factors such as sensitivity to heat, pH, acidity, osmotic effect, mechanical shear, chemical components, freezing and storage time as well which affects the viability of probiotics in the dairy food matrix as well as in the gut. Multiple efforts have been done in the past and ongoing in present for these beneficial microbial population stability until their destination in the gut. One of a useful technique known as microencapsulation makes the probiotic effective in the diversified conditions and maintain these microbe’s community to the optimum level for achieving targeted benefits. Dairy products are found to be an ideal vehicle for probiotic incorporation. It has been seen that the encapsulated microbial cells show higher viability than the free cells in different processing and storage conditions as well as against bile salts in the gut. They make the food functional when incorporated, without affecting the product sensory characteristics.
REPORT-PRESENTATION BY CHIEF SECRETARY, ANDAMAN NICOBAR ADMINISTRATION IN OA ...
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- 1. Inputs from 1. Vision, Mission & Core Values. 2. Environmental & Safety Policy. 3. Occupational Health & Safety Policy. 4. Corporate Social Responsibility 5. Total Productive Maintenance Policy. Inputs from 1. All departments 2. CPCB & SPCB, MOEF 3. Personal Responsibility and Goal Inputs from 1. Environmental Clearance. 2. Consent to Establish. 3. Consent to Operate. 4. Legal and other Requirements. S No Establishment of Environmental Lab Legal and Statutory requirement Pollution Control Device’s Environmental Monitoring & Analysis Interagetd Management System Monitoring & compliance 1 Air Monitoring Lab Application for consent to establishment Complete technical service for all types pollution control systems. Monitoring Schedule as per conditions Application for ISO 9001, ISO 14001 & OHSAS 18001 Monthly Monitoring Report 2 Water Analysis Lab Application for consent to Operate APC equipments operation & maintenance for preventive maintenance patterns. Ambient & Stack Emission Monitoring Interagetd Management System Policy Six Monthly Monitoring Report 3 Microbiology Lab Application for consent to renewal APC equipments spare parts management. Bacteriological analysis IMS Documentations Environmental Statement Report 4 Procurement of instruments, equipment, chemicals, Glass ware etc To meet statutory requirement Al l APC equipments power consumption management. Water& waste water sampling , analysis External, Internal or self Audit and issued the NCR/ Observations. Update new compliance monitoring 5 Infrastructure Dev. for lab Follow up with Pollution Control Board Shut down inspection of ESP, Bag Filters and suggest required maintenance. OHS monitoring Corrective & Preventive Action Monitoring as per New standard 6 Development of Analysis procedures Air Pollution Compliance APC equipment installation, inspection & commissioning. Vehicular Emission Monitoring Co-ordination with other department Other legal monitoring, if any 7 Installation /commissioning/ Operate, maintain & Calibration Solid Waste & Hazardous Waste Compliance etc. Train to staff for ability for coverage area. Infrastructure Development for monitoring Data analysis & discussion and closing NCR/Observations Final discussion with top management Monitoring - Health Safety Air, water, Noise etc Labour License Gate pass Safety PPEs Green belt development Land escaping Plant maintenance Garden development Nursery Development Compliance of conditions through EMPs/QMPs/SOPs/Action Plan on air, water, noise, solid waste etc. Result satisfactory Submission of monitoring results as per compliance status to PCB & MOEF and all concerned. Satisfactory Monitoring Management and Data Analysis Not satisfactory Environment Laboratory, Monitoring Management, APCD’s & Data analysis Environment Health & Safety Safety RAJEEV RANJAN SINGH – ENVIRONMENT HEALTH & SAFETY HorticultureHealth Safety