Quality Management software helps organizations maintain uniformity and consistency in their products and services. It focuses on end-to-end processes, right from the quality of products and services to the activities and means to achieving it and consistently managing it. One such tool is - BM QualityMaster. It allows businesses to improve quality, achieve compliance, decrease risk, and reduce complaints by streamlining their quality management. Check out the PPT to know further-
How to Implement and Maintain an Audit-Ready QMS Leveraging TechnologyGreenlight Guru
Despite ever-changing and increasingly complex medical device regulations, many companies have built their compliance systems on risky paper-based quality systems or legacy, general-purpose software not built for med device. You can do better.
Inefficient systems increase your risk of noncompliance and increase your development time. That translates into missed sales opportunities and patients waiting longer for your new medical technologies.
So we’ll show you a modern, purpose-built software that ensures compliance with all the latest regulations to free up your engineers’ time, reduce risk, time to market, and help you pass audits with flying colors.
• Step-by-step instructions on how to implement and maintain an audit-ready QMS leveraging Jon’s S.M.A.R.T. quality management philosophy
• How to accelerate product development efforts — from napkin idea to 510(k) clearance to market release months or years quicker
• How to manage risk to drive the safety and quality of products and processes through QMS per ISO 13485:2016 & 21 CFR Part 820
• How to change their company’s focus from simply meeting regulations to building quality into their processes as a differentiator
• How to understand and stay ahead of the FDA and EU changing quality regulations as leaders instead of followers
This session took place live at the Greenlight Guru True Quality Virtual Summit, a three-day event for medical device professionals to learn to get their devices to market faster, stay ahead of regulatory changes, and use quality as their multiplier to grow their device business.
Qualityze is an enterprise quality management system (EQMS) built on the salesforce platform It helps manufacturers and other industry suppliers meet their quality and compliance goals by connecting all relevant processes across the company.
Quality Management software helps organizations maintain uniformity and consistency in their products and services. It focuses on end-to-end processes, right from the quality of products and services to the activities and means to achieving it and consistently managing it. One such tool is - BM QualityMaster. It allows businesses to improve quality, achieve compliance, decrease risk, and reduce complaints by streamlining their quality management. Check out the PPT to know further-
How to Implement and Maintain an Audit-Ready QMS Leveraging TechnologyGreenlight Guru
Despite ever-changing and increasingly complex medical device regulations, many companies have built their compliance systems on risky paper-based quality systems or legacy, general-purpose software not built for med device. You can do better.
Inefficient systems increase your risk of noncompliance and increase your development time. That translates into missed sales opportunities and patients waiting longer for your new medical technologies.
So we’ll show you a modern, purpose-built software that ensures compliance with all the latest regulations to free up your engineers’ time, reduce risk, time to market, and help you pass audits with flying colors.
• Step-by-step instructions on how to implement and maintain an audit-ready QMS leveraging Jon’s S.M.A.R.T. quality management philosophy
• How to accelerate product development efforts — from napkin idea to 510(k) clearance to market release months or years quicker
• How to manage risk to drive the safety and quality of products and processes through QMS per ISO 13485:2016 & 21 CFR Part 820
• How to change their company’s focus from simply meeting regulations to building quality into their processes as a differentiator
• How to understand and stay ahead of the FDA and EU changing quality regulations as leaders instead of followers
This session took place live at the Greenlight Guru True Quality Virtual Summit, a three-day event for medical device professionals to learn to get their devices to market faster, stay ahead of regulatory changes, and use quality as their multiplier to grow their device business.
Qualityze is an enterprise quality management system (EQMS) built on the salesforce platform It helps manufacturers and other industry suppliers meet their quality and compliance goals by connecting all relevant processes across the company.
This ppt is informative for the concept of automated manufacturing and the concept of quality planning and analysis. The concept of quality culture is also involved.
In their efforts to decrease costs, improve customer loyalty and extend brand reputation, organizations need a holistic, long-term view of enterprise quality management systems.
4 Quality System Musts for Medtech Startups to Get Safer Products to Market F...Greenlight Guru
Medical device startups have a pile of things to address yet often don’t have the pile of money to take care of everything that is needed. Because of this, a medical device quality system often gets pushed to the back burner in favor of activities that are perceived to add more value and meaning to the startup.
Ignoring a quality system entirely until after development is complete and the product is launched is not a good idea.
A medical device startup should treat the development of a quality management system in a similar fashion as the development of a medical device. Learn how to build your medical device quality system as you go.
Understanding the Medical device Single Audit Program (MDSAP) & How to Prepar...Greenlight Guru
The Medical Device Single Audit Program (MDSAP) is an international initiative spearheaded by the International Medical Device Regulatory Forum (IMDRF) to develop a standardized global approach to auditing and inspecting of medical device manufacturers that will be accepted by multiple regulators to address QMS/GMP requirements.
Although the program has seen relatively low participation to date, the promise to help reduce compliance cost for device makers by eliminating the need for multiple quality system audits and inspections means there is much to be gained by industry from a successful implementation the program.
This presentation will cover:
-Understand the goals and benefits of the MDSAP program
-What are the main differences between MDSAP and standard auditing
-How to benchmark your QMS against the MDSAP
-How the new non-conformance grading system works
-How to prepare your company for a successful MDSAP implementation
Watch the presentation here: https://www.greenlight.guru/webinar/medical-device-single-audit-program-mdsap
EzyPro has expanded its foot print with the integration of computerized maintenance management system. With this from a compliance and quality management system the scope has expanded to a productivity, problem-solving and efficiency enhancing software as a service
free training on Quality Management systems in software industry.Iso 9000,ISO...aaditya
Concerned with ensuring that the required level of quality is achieved in a software product.
Involves defining appropriate quality standards and procedures and ensuring that these are followed.
Should aim to develop a ‘quality culture’ where quality is seen as everyone’s responsibility.
Understanding the who, what, why, and when of quality is essential in implementing an effective Quality Program. It requires a combination of distinct disciplines: Quality Assurance, Quality Control, and Quality Improvement. They are three unique disciplines which, when used together, can improve the efficiency and effectiveness of any organization leading to reduced cost and increased customer satisfaction.
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This presentation originally aired during the 2022 Global MedTech Regulatory Trends Virtual Summit.
This ppt is informative for the concept of automated manufacturing and the concept of quality planning and analysis. The concept of quality culture is also involved.
In their efforts to decrease costs, improve customer loyalty and extend brand reputation, organizations need a holistic, long-term view of enterprise quality management systems.
4 Quality System Musts for Medtech Startups to Get Safer Products to Market F...Greenlight Guru
Medical device startups have a pile of things to address yet often don’t have the pile of money to take care of everything that is needed. Because of this, a medical device quality system often gets pushed to the back burner in favor of activities that are perceived to add more value and meaning to the startup.
Ignoring a quality system entirely until after development is complete and the product is launched is not a good idea.
A medical device startup should treat the development of a quality management system in a similar fashion as the development of a medical device. Learn how to build your medical device quality system as you go.
Understanding the Medical device Single Audit Program (MDSAP) & How to Prepar...Greenlight Guru
The Medical Device Single Audit Program (MDSAP) is an international initiative spearheaded by the International Medical Device Regulatory Forum (IMDRF) to develop a standardized global approach to auditing and inspecting of medical device manufacturers that will be accepted by multiple regulators to address QMS/GMP requirements.
Although the program has seen relatively low participation to date, the promise to help reduce compliance cost for device makers by eliminating the need for multiple quality system audits and inspections means there is much to be gained by industry from a successful implementation the program.
This presentation will cover:
-Understand the goals and benefits of the MDSAP program
-What are the main differences between MDSAP and standard auditing
-How to benchmark your QMS against the MDSAP
-How the new non-conformance grading system works
-How to prepare your company for a successful MDSAP implementation
Watch the presentation here: https://www.greenlight.guru/webinar/medical-device-single-audit-program-mdsap
EzyPro has expanded its foot print with the integration of computerized maintenance management system. With this from a compliance and quality management system the scope has expanded to a productivity, problem-solving and efficiency enhancing software as a service
free training on Quality Management systems in software industry.Iso 9000,ISO...aaditya
Concerned with ensuring that the required level of quality is achieved in a software product.
Involves defining appropriate quality standards and procedures and ensuring that these are followed.
Should aim to develop a ‘quality culture’ where quality is seen as everyone’s responsibility.
Understanding the who, what, why, and when of quality is essential in implementing an effective Quality Program. It requires a combination of distinct disciplines: Quality Assurance, Quality Control, and Quality Improvement. They are three unique disciplines which, when used together, can improve the efficiency and effectiveness of any organization leading to reduced cost and increased customer satisfaction.
Join industry expert, Danny Kroo, key takeaways from the session include: 1. What is MDSAP and when should you consider it? 2. How to prepare for an MDSAP certification audit 3. What are common nonconformities issued by auditing organizations
This presentation originally aired during the 2022 Global MedTech Regulatory Trends Virtual Summit.
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2. IN THIS
PRESENTATION :
• ABOUT CHEMICAL MANUFACTURING
• QUICK STAT-FACT ABOUT CHEMICAL
MANUFACTURING
• WHAT IS CHEMICAL QMS ?
• NEED OF QMS SOFTWARE IN CHEMICAL
INDUSTRY
• BUSINESS ADVANTAGES OF CHEMICAL
INDUSTRY QUALITY MANAGEMENT
SOFTWARE
• BM QUALITYMASTER : NEXT-GEN EQMS
FOR MANAGING CHEMICAL INDUSTRY’S
QUALITY NEED
• WHAT BM QUALITYMASTER CAN DO TO
YOUR BUSINESS ?
• HOW IT HELPS?
• MODULES OF BM QUALITYMASTER
• WHY BM QUALITYMASTER ?
• CONCLUSION
3. ABOUT CHEMICAL
MANUFACTURING
• Chemical manufacturers produce products by transforming organic
and inorganic raw materials with chemical processes.
• Their operations require them to manage material quality, packaging,
environmental problems, toxic spills, compliance, employee safety,
etc.
• Out of these, preserving quality and abiding by the strict rules that are
imposed by the government are the key essentials.
• Why? Because compromising on the quality of these harmful/toxic
substances can cost them a boatload and can be hazardous for
consumers.
• Therefore, they need a comprehensive quality management software
to align all their quality related operations and establish a streamlined
workflow.
4. QUICK STAT-FACT ABOUT
CHEMICAL MANUFACTURING
• The chemical industry of India is a major industry in the Indian
economy and as of 2022, contributes 7% of the country's Gross
Domestic Product (GDP).
• India is the world's sixth largest producer of chemicals and the third
largest in Asia, as of 2022.
• Demand for chemical products is expected to grow at approximately
9% p.a. during 2020-2025 (https://www.investindia.gov.in/sector/chemicals )
• The Chemicals and Petrochemicals market is projected to reach
$300 billion by 2025 (https://www.investindia.gov.in/sector/chemicals )
5. WHAT IS A CHEMICAL QMS ?
Chemical Quality Management Software is a formalized system of
processes that helps firms in locating and resolving the fundamental
problems with product quality so they may get closer to the quality
objective they have set.
There are several uses for a QMS for chemical industry, including:
Raw material quality handling
Supplier check for quality purchasing
Managing product formulation to ensure consistency
Hazard management
Controlling & managing complete manufacturing process
Adhering to product standards
Packaging & labelling
6. NEED OF QMS SOFTWARE IN
CHEMICAL INDUSTRY
• Chemical manufacturers generally struggle to increase
efficiency, improve compliance, or produce higher-quality
goods without a chemical QMS software.
• Without a comprehensive specialty chemical
manufacturing software, they might fail to :
- Optimize their quality processes
- Get the resolutions of customer complaints
- Determine non-conformities
- Conduct audit activities
- Create important policies and
- Manage, secure and organize documents
7. BUSINESS ADVANTAGES OF
CHEMICAL INDUSTRY QUALITY
MANAGEMENT SOFTWARE
A right QMS System will not only streamline quality processes but will
also increase efficiency. It will also set your company apart from the
league. Here’s how –
• Tracks all nonconformities
• Provides powerful reporting & analytics capabilities
• Resolves customer complaints & queries
• Establishes a secured workflow for documentations
• Complies with regulatory requirements
• Maintains SOPs at one place
• Automates the audit processes
• Controls risk exposure
• Ensures continuous process improvement
8. BM QUALITYMASTER :
A NEXT-GEN EQMS FOR
MANAGING CHEMICAL
INDUSTRY’S QUALITY NEEDS
• It is an advanced QMS for chemical industry that offers better
visibility into and traceability of quality processes to chemical
manufacturers.
• It also helps in inspecting their manufacturing process, mitigating
risks, controlling & optimizing supplier quality, manage documents,
handle quality audits, along with effectively managing customer
complaints.
• With its feature-rich dashboards and customizable reports it brings
the entire organization on the same page regarding the regulatory
standards for safety, health and environmental care.
9. WHAT BM QUALITYMASTER
CAN TO YOUR BUSINESS ?
• BM QualityMaster incorporates the rest of the business in
terms of the legal duties for environmental, health, and safety
protection.
• By adhering to sops, providing deviation alerts, and following
the industry best practices, chemical producers can produce a
product of consistent quality.
• With its wide range of modules for quality and compliance
management, it elevates organizations into a collaborative and
paperless environment for ongoing improvement.
• It helps in lowering the overall administrative costs of
maintaining quality at every stages of production
• Being a cloud-based QMS software, it ensures that every stage
of the process is coordinated and compliant by creating a single
source of truth for goods, processes, and quality data.
10. HOW IT DOES THIS ?
• Maintains an audit trail of documents viewed,
accessed, and modified by any user
• Tracks nonconformity records and suggests
preventive actions accordingly
• Records the corrective measures taken to
prevent the recurrence of non-conformance
• Performs verification and maintains the
effectiveness of CAPA or any other vital
information related to the CAPA verification
process
• Stores documents in a centralized database for
resolving customer complaints
• Supports change management cycle
12. MODULES OF
BM QUALITYMASTER
This software possesses a wide array of features. Check them out
below:
•Non-Conformance – Efficiently capture, manage and track non-
conformance issues. Perform root cause analysis.
•CAPA – Identify quality issues, execute containment actions, mitigate
recurrence & verify the effectiveness of root cause elimination.
•Complaint Management – Helps investigate, track and resolve quality
related complaints right from identification to resolution.
•Training Management – Automate training processes & keep accurate
training records.
13. MODULES OF
BM QUALITYMASTER
•Change Management – Establish a proper document workflow &
automate change control processes.
•Document Management – Store, create, track, retrieve & manage
organizational documents.
•Compliance Management – Make a clear list of requirements. Automate
alerts for potential issues to manage compliance.
•Risk Management – Assess future risks and their impact. Drive
continuous process improvement through risk control and mitigation.
•Audit Management – Automate & streamline the process of planning,
scheduling & conducting audits
14. WHY BM QUALITYMASTER ?
BM QualityMaster for Chemicals is a powerful, scalable and easy-to-use
TQM software that allows manufacturers achieve quality standards,
compliance along with reducing costs and customer complaints.
Choosing this software is always “Win-Win” situation, because it:
- Can be implemented quickly and has simple UI/UX
- Can scale your business needs and growth
- Can seamlessly integrate with other software and enhance
functionalities
- Can offer data confidentiality & integrity with its cloud-based
approach
- Offers low-cost deployment and data migration
- Available on several platform such as: cloud, on-premise & hybrid
- Can be accessible 24*7 , anywhere through any device
- Provides a personalized dashboard to access the business workflows
directly.
15. CONCLUSION
• The chemical industry works under high regulations and deals with
high toxic chemicals. Hence, each and ever chemical manufacturing
company should incorporate efficient tools to ensure safe and quality
products.
• Implementing a competent QMS for chemical industry, like BM
QualityMaster definitely provides a major help to the manufacturers
to streamline their core operations, monitor product quality, and get a
competitive edge from the competitors by having better problem
solving approaches.
• Get in touch with our experts today and know how this software can
be useful for you.
16. Contact Us
BatchMaster Software Pvt. Ltd.
(An ISO 9001:2015 Certified Company)
Brilliant Solitaire Plot 6-A
Office 201-A to 204-B
Scheme 78, Part-II,
Indore – 452010
+91-731-4008039
+91-731-4008070
+91-731-4008035
Email:
contact@bmqualitymaster.com
About Us
BM QualityMaster is a product of BatchMaster
Software Pvt. Ltd. From last 20 plus years, we
are a leading business software development
company with noteworthy ERP, QMS, HRMS
and other technological products. we have
offices around the globe to serve customers
from all geographies and industries.