Quality Management in General 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 This reactive approach to quality management is costly, dangerous, outdated, and arguably the foremost obstacle to long-term growth.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 Quality Management Software 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 9000, AS 9100, ISO/IATF/TS 16949, ISO 13485, FDA 21 CFR Part 11, HACCP/ISO 22000, ISO 14000, and FDA GxP.
ISO 9000 Compliance
Quality management and quality assurance would not be what they are today without ISO 9000. 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 9000 requirements are met while making the set of standards work in your favor. Learn how IQS transforms the management of ISO 9000 (ISO 9001:2015).
AS 9100 Compliance
If managed without the proper knowhow 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.
ISO/IATF/TS 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 ISO/IATF/TS 16949 standards. IQS Quality Management and Compliance Software removes the burden of ISO/IATF/TS 16949 initiatives, so you can focus on delivering products on schedule and at the best cost. Learn why you can’t manage ISO/IATF/TS 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 Quality Management and Compliance Software 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 Quality Management Software. IQS takes an enterprise-wide approach to FDA 21 CFR Part 11, leveraging integrated document management and 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 Quality Management Software 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 Quality Management Software 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 Quality Management Software 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.