Inspection Software

AS9102B: First Article Inspection with Inspection Management Software

The aerospace industry is one of the most highly regulated industries in the world, requiring rigorous quality control measures to ensure the safety and reliability of its products. One such measure is the AS9102B, a standard that provides a comprehensive framework for first article inspection (FAI) in the aerospace sector. This article will delve into the details of AS9102B, discussing its importance, scope, and key components, and how our newest Inspection Management Software, can help you to better meet your requirements for FAI.

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Eqms Software

Pharmaceutical eQMS Software Validation Best Practices

As part of different regulatory requirements for pharmaceutical industry standards, the eQMS software needs to comply with several quality specifications and regulatory requirements for US FDA Title 21 CFR Part 11 Electronic Records and Electronic Signatures guidelines, US FDA Title 21 CFR Part 820 Document Controls guidelines, EU Annex 11 Computerized Systems guidelines, ISO 13485:2016 Control of Documents and Control of Records guidelines, and other GMP guidelines. As a result, the Computerized System Validation (CSV) is the prime requirement for any Pharmaceutical eQMS Software. To help pharmaceutical industry with this validation process, IntellaQuest incorporates the complete validation service along with its eQMS software package and quality consultancy.

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Medical Device risk management

How ISO 14971 Helps Medical Device Firms Better Meet QMS Risk Management Requirements

In the rapidly evolving world of medical device manufacturing, ensuring the safety and efficacy of products is of paramount importance. Manufacturers face a multitude of regulatory requirements designed to minimize risks to patients and healthcare providers while promoting innovation. Among these standards, ISO 14971 and ISO/TR 24971 play a crucial role in guiding medical device manufacturers through the process of risk management, and they play an important role in the implementation of a QMS that meets the requirements of ISO 13485. In this article, we will delve into the importance of ISO 14971, explore the complementary role of ISO/TR 24971, and discuss their applications in the medical device industry.

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EHS Management Software

A Company’s EHS Management Role in Accelerating Change Towards Water Conservation 

Water is an indispensable resource for all life forms on Earth, underpinning the functionality of ecosystems, agriculture, industry, and human survival. Its vital role encompasses drinking, cooking, sanitation, and hygiene, and it is pivotal in the production of food and goods. Uncontaminated and secure water access is a fundamental human entitlement; its absence can lead to poverty, disease, and conflict. Consequently, the preservation and judicious exploitation of water resources is pivotal for guaranteeing the prosperity of present and forthcoming generations. Within the framework of EHS Management, safeguarding these resources is integral to ensuring comprehensive quality management across all industry sectors.

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Overcoming Common PPAP Challenges That Lead to OEM Rejections

PPAP is a critical step in the automotive supply chain that is meant to ensure the quality of parts being produced by suppliers. The PPAP process is used by automotive OEMs to verify that the parts produced by suppliers meet their specifications, quality standards, and other requirements. However, submitting PPAP can be a challenging process, and there are many reasons why OEM customers reject initial PPAP submissions. Read on to learn more.

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EHS Management System

11 Pragmatic Ways for an Organization to Reduce their Carbon Footprint 

Climate change is a global issue which requires a coordinated global response. Countries have made commitments to reducing their greenhouse gas emissions and transitioning to cleaner energy sources. The private sector has also stepped up, with businesses pledging to reduce their carbon footprint and invest in renewable energy. Although there is visible progress, there is still a lot of work to be done, and continued global cooperation and action are essential to addressing the impacts of climate change. This article explores 11 pragmatic ways for an organization to reduce their carbon footprint.

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Quality Control

Quality Planning, Quality Control, and Quality Improvement with Inspection Management Software

Quality planning, control, and improvement are integral components of ensuring that products and services meet or exceed customer expectations. One key aspect of quality planning is a well-defined inspection plan, which is a set of procedures and guidelines used to inspect and evaluate products and services. Inspection plans help to ensure consistency and accuracy in the inspection process, identify potential problems early on, improve communication and collaboration between different departments, and reduce costs.

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