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jack 2023-11-20
As businesses strive to optimize their workflows, it's imperative to delve into the future trends shaping document management. Shift to Cloud-Based Document ManagementCloud computing has emerged as a game-changer in document management. Mobile Document ManagementThe future of document management is mobile. Compliance and Regulatory ConsiderationsAdapting document management systems to comply with regulations is non-negotiable. ConclusionIn conclusion, the future of document management is dynamic and promising.
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jack 2021-05-11
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This whitepaper explains about Embracing Enterprise Quality Management Systems to help migrate from paper based, be-spoke/non-integrated systems to a unified platform providing capabilities to automate key QMS processes across the organization.

Companies, as part of their digital transformation, embrace Enterprise Quality Management Systems to help migrate from paper based, be-spoke/non-integrated systems to a unified platform providing capabilities to automate key QMS processes across the organization.

As such, the question that often asked is, which solution(s) should I start with?

The typical consultant response would be, “Start with where you believe the maximum pain for the organization is and evolve from there”. 

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0
jack 2021-05-11
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This whitepaper documents ComplianceQuest’s position regarding compliance to Good Manufacturing Practice Medicinal Products For Human And Veterinary Use – Annex 11: Computerized Systems System Requirements  Some industrial segments need to be exponentially stringent with their quality and compliance processes compared to other segments.

The Life Science industry is part of this stringent segment.

They need to ensure the quality of their products because they deal with human safety.

The accuracy and efficiency of their work could well be a matter of life and death.

collect
0
jack 2021-05-10
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The QMS enables this by centralizing the quality management system, thereby providing an organization-wide view of data, information and processes.

A QMS ensures consistent quality of products and processes, mid-course corrections, root cause analysis in case of any problems and deviations, audit management, supplier customer relationship management, complaints handling as well as continuous improvement.

collect
0
jack 2022-05-04
img
The European Medical Device Regulation (EU MDR), a robust, transparent, predictable and sustainable regulatory framework for medical devices, ensures high standards of quality and safety being produced in or supplied into Europe. By improving the safety and performance of medical devices, the EU MDR regulations are intended to improve the safety of healthcare and the performance of medical devices in Europe. To do this, the EU MDR regulations aim to create a new and improved landscape for the quality and safety of medical devices with the following new guidelines:An independent assessment of all medical devices for safety and performance before they can be marketed in the EUMore transparent information on the benefits for patients, residual risks, and a comprehensive assessment of the overall risk/benefit ratio Clear rules to enable standardization and support simpler and less complex trading between EU member states; those that do not comply will be penalizedNew rules to support patient-oriented innovation and take particular account of the specific needs of the many small and medium-sized manufacturers in this sectorPlace further responsibilities on “Notified Bodies”, an independent third party that performs conformity assessments for medium and high-risk devicesrefer: eu mdrhttps://www. compliancequest. com/regulations/what-is-eu-mdr/
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0
jack 2021-05-11
img

This WhitePaper gives clear idea about Importance of Quality Management System and Salesforce for Faster Path to Compliance Manufacturers are responsible for the safety and quality of their products.

Legislators, the general public and manufacturers, themselves, recognize this indisputable fact.

Yet, this wasn’t always the case.Take the automotive industry, for example.

For most of the 20th century, American carmakers actually opposed the idea of assuming responsibility for product design flaws.

Unfortunately, it took a repeated loss of life to change this.

collect
0
jack 2021-05-11
img

Read this whitepaper to understand the 5 challenge areas that most businesses will face and how Quality can become a lever of your Business Continuity strategy.

Usually disasters are in the form of nature’s fury that disrupts lives, but this time, for the first time since the dawn of the digital age, the world is seeing a global lockdown of extraordinary magnitude.

Both digital and physical infrastructure are intact, but a deadly virus has largely crippled the movement of people and created economic destruction worldwide.

collect
0
jack 2021-05-10
img

In this whitepaper we delve deeper into these guiding principles that make the ComplianceQuest EQMS “next generation” and how it can help lead your organization towards Quality Excellence.

In today’s interconnected, complex world, quality and operational excellence frameworks like Lean and Six Sigma are simply not enough by themselves.

The smart enterprise of the future will need a quality system that is agile, flexible, connected and data-driven.

It should not only drive the execution of quality processes but help future-oriented teams innovate and move forward.

It should empower teams to learn and pick up new skills through training, quickly navigate between supplier, customer and internal dashboards and generate insights from quality and operational metrics.

collect
0
jack 2022-05-04
img
What is ISO 14001 Certification? Why is ISO 14001 Certification important? What are the practical steps for ISO 14001 Certification? Therefore, to provide the infrastructure to achieve ISO 14001, most EHS experts are trying to meet ISO 14001 standards relying on an environmental software platform. One of the most effective methods of achieving ISO 14001 certification and maintaining ISO status is the Environmental Software platform as it essentially provides a centralized digital platform for ISO documentation and a place to track environmental goals or KPIs that establish the right path for ISO 14001 certification.
collect
0
jack 2021-05-11
img

The goal of this whitepaper is to provide a simple guideline to help our readers think through the process of embracing digital transformation tools and techniques, as they gear up for the next level of quality and compliance within their enterprise.

Today, quality leaders have to embrace the world of digital transformation, taking advantage of the latest developments in cloud, mobile and digital technologies to make their jobs easier.Quality and compliance in today’s scenario is a collaborative effort.

It requires a seamless flow of data and key metrics across the entire supply chain and lifecycle of an organization.

It involves tracking quality events across suppliers, while simultaneously tracing customer experience and complaints.

It requires a nimble footed approach to taking corrective action, and all this is possible only through automation.

collect
0
jack 2021-05-10
img

This white paper will introduce an innovative quality suite that can help life science companies digitally transform their content and quality management As life science companies embrace the benefits of cloud computing, those who are most innovative are identifying additional ways to streamline their business and quality operations.

An effective electronic Content Management System points to the need for an Enterprise Quality Management System (EQMS) that incorporates document, training/learning, and change management.

collect
0
jack 2021-05-10
img

This Whitepaper explains A step-by-step approach to assess and rebuild your organization’s supply with ComplianceQuest Solutions.

Over the last few years at ComplianceQuest, we have had the privilege of working with many supply chain leaders, helping them automate their supplier management process.

It is a part of the ComplianceQuest QHSE (Quality, Health, Safety and Environmental Management) suite, and we have witnessed first-hand the power of automation in helping mitigate risk and fixing inefficiencies in key supplier management processes.

collect
0
jack 2022-05-03
img
The software supports each aspect of your own change management process from initiation and review/approval through to execution tracking, verification and closure. The backbone of any quality system, CQ Change Management connects automatically with other QMS processes including CAPA, Document Management and Training Management to ensure seamless integration between QMS processes. Establish and Follow Best PracticesSystematically follow proper procedures and practices when rolling out changes. Streamline the process and guarantee consistency and repeatability across the entire change process. Increase Change VisibilityTrack all change actions and related impact to understand how changes are progressing.
collect
0
jack 2021-05-11
img

This whitepaper documents ComplianceQuest’s position regarding compliance to Electronic Records; Electronic Signatures 21 CFR Part 11.

Some industrial segments need to be exponentially stringent with their quality and compliance processes compared to other segments.

The Life Science industry is part of this stringent segment.

They need to ensure the quality of their products because they deal with human safety.

The accuracy and efficiency of their work could well be a matter of life and death.

collect
0
jack 2021-05-10
img

The accuracy and efficiency of the devices’ performance could well be a matter of life and death.

Successful implementation of quality best practices for medical device companies requires a simple 7-Step approachMore than any other industrial segment, medical device manufacturers need to ensure the quality of their products because they deal with human safety.

collect
0
jack 2021-05-10
img

In this whitepaper, we focus on seven distinct advantages of implementing a unified system for quality and safety.

At ComplianceQuest, we have tremendous experience in the area of quality and compliance.

We’ve led the digital transformation and automation of quality processes for customers in over 800 locations worldwide.

With the current COVID19 pandemic, enterprises are forced to look at new processes and workflows related to health, safety, and the environment.

To implement these processes well, automation and digital transformation are crucial.

collect
0
jack 2023-11-20
As businesses strive to optimize their workflows, it's imperative to delve into the future trends shaping document management. Shift to Cloud-Based Document ManagementCloud computing has emerged as a game-changer in document management. Mobile Document ManagementThe future of document management is mobile. Compliance and Regulatory ConsiderationsAdapting document management systems to comply with regulations is non-negotiable. ConclusionIn conclusion, the future of document management is dynamic and promising.
jack 2022-05-04
img
What is ISO 14001 Certification? Why is ISO 14001 Certification important? What are the practical steps for ISO 14001 Certification? Therefore, to provide the infrastructure to achieve ISO 14001, most EHS experts are trying to meet ISO 14001 standards relying on an environmental software platform. One of the most effective methods of achieving ISO 14001 certification and maintaining ISO status is the Environmental Software platform as it essentially provides a centralized digital platform for ISO documentation and a place to track environmental goals or KPIs that establish the right path for ISO 14001 certification.
jack 2021-05-11
img

This whitepaper explains about Embracing Enterprise Quality Management Systems to help migrate from paper based, be-spoke/non-integrated systems to a unified platform providing capabilities to automate key QMS processes across the organization.

Companies, as part of their digital transformation, embrace Enterprise Quality Management Systems to help migrate from paper based, be-spoke/non-integrated systems to a unified platform providing capabilities to automate key QMS processes across the organization.

As such, the question that often asked is, which solution(s) should I start with?

The typical consultant response would be, “Start with where you believe the maximum pain for the organization is and evolve from there”. 

jack 2021-05-11
img

The goal of this whitepaper is to provide a simple guideline to help our readers think through the process of embracing digital transformation tools and techniques, as they gear up for the next level of quality and compliance within their enterprise.

Today, quality leaders have to embrace the world of digital transformation, taking advantage of the latest developments in cloud, mobile and digital technologies to make their jobs easier.Quality and compliance in today’s scenario is a collaborative effort.

It requires a seamless flow of data and key metrics across the entire supply chain and lifecycle of an organization.

It involves tracking quality events across suppliers, while simultaneously tracing customer experience and complaints.

It requires a nimble footed approach to taking corrective action, and all this is possible only through automation.

jack 2021-05-11
img

This whitepaper documents ComplianceQuest’s position regarding compliance to Good Manufacturing Practice Medicinal Products For Human And Veterinary Use – Annex 11: Computerized Systems System Requirements  Some industrial segments need to be exponentially stringent with their quality and compliance processes compared to other segments.

The Life Science industry is part of this stringent segment.

They need to ensure the quality of their products because they deal with human safety.

The accuracy and efficiency of their work could well be a matter of life and death.

jack 2021-05-10
img

This white paper will introduce an innovative quality suite that can help life science companies digitally transform their content and quality management As life science companies embrace the benefits of cloud computing, those who are most innovative are identifying additional ways to streamline their business and quality operations.

An effective electronic Content Management System points to the need for an Enterprise Quality Management System (EQMS) that incorporates document, training/learning, and change management.

jack 2021-05-10
img

The QMS enables this by centralizing the quality management system, thereby providing an organization-wide view of data, information and processes.

A QMS ensures consistent quality of products and processes, mid-course corrections, root cause analysis in case of any problems and deviations, audit management, supplier customer relationship management, complaints handling as well as continuous improvement.

jack 2021-05-10
img

This Whitepaper explains A step-by-step approach to assess and rebuild your organization’s supply with ComplianceQuest Solutions.

Over the last few years at ComplianceQuest, we have had the privilege of working with many supply chain leaders, helping them automate their supplier management process.

It is a part of the ComplianceQuest QHSE (Quality, Health, Safety and Environmental Management) suite, and we have witnessed first-hand the power of automation in helping mitigate risk and fixing inefficiencies in key supplier management processes.

jack 2022-05-04
img
The European Medical Device Regulation (EU MDR), a robust, transparent, predictable and sustainable regulatory framework for medical devices, ensures high standards of quality and safety being produced in or supplied into Europe. By improving the safety and performance of medical devices, the EU MDR regulations are intended to improve the safety of healthcare and the performance of medical devices in Europe. To do this, the EU MDR regulations aim to create a new and improved landscape for the quality and safety of medical devices with the following new guidelines:An independent assessment of all medical devices for safety and performance before they can be marketed in the EUMore transparent information on the benefits for patients, residual risks, and a comprehensive assessment of the overall risk/benefit ratio Clear rules to enable standardization and support simpler and less complex trading between EU member states; those that do not comply will be penalizedNew rules to support patient-oriented innovation and take particular account of the specific needs of the many small and medium-sized manufacturers in this sectorPlace further responsibilities on “Notified Bodies”, an independent third party that performs conformity assessments for medium and high-risk devicesrefer: eu mdrhttps://www. compliancequest. com/regulations/what-is-eu-mdr/
jack 2022-05-03
img
The software supports each aspect of your own change management process from initiation and review/approval through to execution tracking, verification and closure. The backbone of any quality system, CQ Change Management connects automatically with other QMS processes including CAPA, Document Management and Training Management to ensure seamless integration between QMS processes. Establish and Follow Best PracticesSystematically follow proper procedures and practices when rolling out changes. Streamline the process and guarantee consistency and repeatability across the entire change process. Increase Change VisibilityTrack all change actions and related impact to understand how changes are progressing.
jack 2021-05-11
img

This WhitePaper gives clear idea about Importance of Quality Management System and Salesforce for Faster Path to Compliance Manufacturers are responsible for the safety and quality of their products.

Legislators, the general public and manufacturers, themselves, recognize this indisputable fact.

Yet, this wasn’t always the case.Take the automotive industry, for example.

For most of the 20th century, American carmakers actually opposed the idea of assuming responsibility for product design flaws.

Unfortunately, it took a repeated loss of life to change this.

jack 2021-05-11
img

This whitepaper documents ComplianceQuest’s position regarding compliance to Electronic Records; Electronic Signatures 21 CFR Part 11.

Some industrial segments need to be exponentially stringent with their quality and compliance processes compared to other segments.

The Life Science industry is part of this stringent segment.

They need to ensure the quality of their products because they deal with human safety.

The accuracy and efficiency of their work could well be a matter of life and death.

jack 2021-05-11
img

Read this whitepaper to understand the 5 challenge areas that most businesses will face and how Quality can become a lever of your Business Continuity strategy.

Usually disasters are in the form of nature’s fury that disrupts lives, but this time, for the first time since the dawn of the digital age, the world is seeing a global lockdown of extraordinary magnitude.

Both digital and physical infrastructure are intact, but a deadly virus has largely crippled the movement of people and created economic destruction worldwide.

jack 2021-05-10
img

The accuracy and efficiency of the devices’ performance could well be a matter of life and death.

Successful implementation of quality best practices for medical device companies requires a simple 7-Step approachMore than any other industrial segment, medical device manufacturers need to ensure the quality of their products because they deal with human safety.

jack 2021-05-10
img

In this whitepaper we delve deeper into these guiding principles that make the ComplianceQuest EQMS “next generation” and how it can help lead your organization towards Quality Excellence.

In today’s interconnected, complex world, quality and operational excellence frameworks like Lean and Six Sigma are simply not enough by themselves.

The smart enterprise of the future will need a quality system that is agile, flexible, connected and data-driven.

It should not only drive the execution of quality processes but help future-oriented teams innovate and move forward.

It should empower teams to learn and pick up new skills through training, quickly navigate between supplier, customer and internal dashboards and generate insights from quality and operational metrics.

jack 2021-05-10
img

In this whitepaper, we focus on seven distinct advantages of implementing a unified system for quality and safety.

At ComplianceQuest, we have tremendous experience in the area of quality and compliance.

We’ve led the digital transformation and automation of quality processes for customers in over 800 locations worldwide.

With the current COVID19 pandemic, enterprises are forced to look at new processes and workflows related to health, safety, and the environment.

To implement these processes well, automation and digital transformation are crucial.