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Quality in Manufacturing

Quality Management for Manufacturing

Manufacturers have been struggling with quality management since the dawn of production. The very nature of processes that demand precision down to the most finite specifications, administering partnerships between engineering and operations, getting the most out of global supplier relationships, and everything else required to take a product from ideation through delivery is as difficult to manage as it is crucial to business performance.

It’s time to stop managing quality and compliance in general manufacturing like they’re just any old item on your list of priorities. The vision of operational excellence should be right around the corner, when in reality too many manufacturers are operating with a set of disjointed homegrown and legacy systems. This reactive approach to quality management is costly, dangerous, outdated, and arguably the foremost obstacle to long-term growth.

IQS software focuses on quality management for manufacturing and cuts through the complexities of manufacturing operations. It elevates quality management systems, optimizing the connection between your people, processes, and modern technology. Under one integrated solution, IQS helps manage your quality systems and compliance mandates including ISO 9001, AS 9100, IATF 16949, ISO 13485, FDA 21 CFR Part 11, HACCP/ISO 22000, ISO 14000, and FDA GxP.

 

ISO 9001:2015 Compliance

Quality management and quality assurance would not be what they are today without ISO 9001. Adhering to the ISO 9000 family of standards is a requirement in most manufacturing settings, although maintaining industry compliance can be challenging at scale and when international borders are a factor. Built upon a foundation of compliance, IQS ensures ISO 9001 requirements are met while making the set of standards work in your favor. Learn how IQS transforms the management of ISO 9001:2015.

 

AS 9100 Compliance

If managed without the proper know-how or systems in place, the aerospace and defense industry’s unique set of compliance requirements can be inhibiting. AS 9100 compliance standards provide a framework for managing compliance. They are designed to identify possible vulnerabilities within quality management systems in aerospace and defense. IQS takes an integrated approach to AS 9100, helping companies demonstrate compliance in a streamlined and less costly way. Learn how IQS’s integrated approach to AS 9100 compliance works.

 

IATF 16949 Compliance

If recent high-profile events have taught us anything, it’s that quality management is at the heart of long-term success in the automotive industry. Regulations and standards are evolving, and maintaining compliance means keeping pace with the corresponding set of IATF 6949 standards. IQS Compliance and Quality Management Software for manufacturing removes the burden of IATF 16949 initiatives, so you can focus on delivering products on schedule and at the best cost. Learn why you can’t manage IATF 16949 without IQS software.

 

ISO 13485 Compliance

Medical device manufacturing is an industry known for world-changing innovations. But—rightly so—the complexities of manufacturing processes and their connection to the health and safety of individuals face high levels of scrutiny and compliance. IQS software for compliance and quality management for manufacturing incorporates deep industry expertise and knowledge of ISO 13485, so manufacturers can continue bringing new and innovative products to the world without being held back by dynamic domestic and international regulations. Learn how IQS takes a platform approach to ISO 13485 compliance.

 

FDA 21 CFR Part 11 Compliance

Effectively managing records and signatures is imperative for medical device, pharmaceuticals, and other types of manufacturing overseen by the FDA. To avoid getting bogged down by hefty FDA 21 CFR Part 11 documentation requirements, leading companies are deploying IQS software for compliance and quality management. IQS takes an enterprise-wide approach to FDA 21 CFR Part 11, leveraging integrated document control modules. Learn how FDA 21 CFR Part 11 and IQS software go hand in hand.

 

HACCP/ISO 22000 Compliance

For the food and beverages industry, the risk of recalls and other food safety-related issues could be virtually eliminated with a leading-edge quality management system supported by next-generation technology. Having a sound solution in place for managing HACCP/ISO 22000 compliance is a staple of a mature process manufacturing organization. IQS software for compliance and quality management for manufacturing applies industry expertise to HACCP/ISO 22000 compliance, ensuring standards are continuously met. Learn why F&B needs IQS for HACCP/ISO 22000 compliance.

 

EH&S/ISO 14000 Compliance

The environmental impacts of production have been under a microscope for decades. Touching every manufacturing industry in a unique way, EH&S and the ISO 14000 family of standards aim to reduce ways organizations negatively impact the environment. The challenge for manufacturing is there is no one-size-fits all approach to managing EH&S and ISO 14000 compliance. IQS software for compliance and quality management for manufacturing provides industry-specific solutions for the always-evolving set of environmental standards. Learn how EH&S/ISO 14000 requirements vary by industry.

 

FDA GxP Compliance

In the competitive world of medical device manufacturing, where innovation and time-to-market are key determinants of success, receiving citations from the FDA can take your momentum to a screeching halt. In order to maintain the level of speed needed to be competitive, organizations must adhere to FDA GxP mandates. IQS software for compliance and quality management for manufacturing aligns your actions with FDA GxP mandates, helping you easily remain compliant even in the most complex scenarios. Learn how IQS helps you manage GxP Compliance.

IQS Manufacturing Customers

IQS yields actionable insight into performance, cost of quality and risk-related metrics including real-time visibility on supplier quality, production and customer satisfaction. All things to help you maintain a competitive advantage. Here is a sampling of IQS customers in this industry who trust IQS for their quality management and compliance software needs.

customer_MTD Products_IQS
customer_panasonic_IQS
customer_Sealy_IQS
customer_Stanley_IQS
customer_Thomas&Betts_IQS
customer_worthington_IQS

LEARN MORE ABOUT THE CORE IQS QMS SOFTWARE PROCESSES:

Case Study How to Get Started with Performance Management

To gain a better understanding into the foundations of a strong quality performance management program, this report will focus on highlights from the recent LNS Research Global Executive Council meeting. In the meeting, Vice President of Quality & Lean Systems and Environment, Health, and Safety at Accuride Corporation, Jd Marhevko, shared best practices as well as her alternative approach to performance management. She and her team leverage a quality improvement methodology known as the Cost of Poor Execution (COPE).
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Quality 4.0 Get Educated, Get Involved, and Build a Successful Strategy

IQS understands that the responsibilities of industry leaders include effectively leveraging rapid change and creating an aggressive strategy for corporate success that aligns with quality management objectives. A recent research study developed by LNS Research, “Quality 4.0: Get Educated, Get Involved, and Build a Successful Strategy,” elucidates exactly how corporate leaders can utilize a powerful knowledge base to construct an informed direction in the marketplace. Digital transformation in terms of quality is  about placing your business on the path to dominance.
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Balancing the Cost of Quality IT Investments and Integrated QMS

In today’s global manufacturing industry, balancing the cost of quality, IT investments, and integrated QMS (quality management systems) presents as a never-ending series of challenges for your company.  To implement an integrated quality management solution effectively, you need to win buy-in from all stakeholders, particularly stakeholders in your company’s IT department.  The fact of the matter is that IT, too, has been forced to do more with less resources, which makes maximizing returns on previous technology investments all the more critical.
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