The Risks of One-Size-Fits-All Security

Security concerns differ from industry to industry. So why do many businesses settle for one-size-fits-all security systems? Discover the potential threats to businesses such as car dealerships, restaurants and retailers, and the ways you can better pr…

Providing the Greatest Service: Protection

Your business plays a vital role in the community. As health-, personal- and business-oriented service providers, you deliver the goods and services people depend on daily. And as the backbone of society, it’s imperative that your business is protected…

Next Generation Bill of Materials (BOM)

In the world of product design and manufacturing, the bill of materials (BOMs) is a critical product information record for both the engineering and manufacturing teams. Managing BOMs with the wrong tools can cause product errors, delays and compliance…

5 Tips for Getting Executive Backing for a New or Expanded EQMS

If you and your team are responsible for improving the efficiency and effectiveness of quality and compliance in your organization, sooner or later you are likely to face a challenge—getting the support of executives and other departments in either establishing or expanding an electronic quality management system (EQMS).

Most executives cite the high cost of adopting technology as the main reason they reject plans to buy software or expand system usage. There are many reasons for interdepartmental resistance to system adoption, but the most common is the lack of understanding of the value of quality.

This white paper is based on a MasterControl group discussion that explored the underlying factors behind executive and organizational opposition to an electronic quality system. The participants came from regulated companies that use MasterControl software.

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How Effective Training Management Can Help You Prevent Quality Issues

It’s not enough to have your quality standards on paper. You have to implement and integrate them into your daily operations and prove to regulators that your standards and policies work. “Effective training should be a fundamental part of a company’s quality management strategy as it can help prevent many quality problems from ever occurring,” said Hunter.

In a regulated environment, training is a means to minimize (if not avoid) human error, a common cause of deviations and nonconformances. It’s no wonder that various standards and regulations, such as the following, require training as an integral part of the quality management system.

  • FDA 21 CFR Part 211.25 for pharmaceutical companies
  • FDA 21 CFR Part 820.25 for medical device manufacturers
  • ISO 9000 2000 for general manufacturers and other businesses
  • ISO 13485 for medical device manufacturers

Request Free!

5 Tips for Getting Executive Backing for a New or Expanded EQMS

If you and your team are responsible for improving the efficiency and effectiveness of quality and compliance in your organization, sooner or later you are likely to face a challenge—getting the support of executives and other departments in either establishing or expanding an electronic quality management system (EQMS).

Most executives cite the high cost of adopting technology as the main reason they reject plans to buy software or expand system usage. There are many reasons for interdepartmental resistance to system adoption, but the most common is the lack of understanding of the value of quality.

This white paper is based on a MasterControl group discussion that explored the underlying factors behind executive and organizational opposition to an electronic quality system. The participants came from regulated companies that use MasterControl software.

Request Free!

How Effective Training Management Can Help You Prevent Quality Issues

It’s not enough to have your quality standards on paper. You have to implement and integrate them into your daily operations and prove to regulators that your standards and policies work. “Effective training should be a fundamental part of a company’s quality management strategy as it can help prevent many quality problems from ever occurring,” said Hunter.

In a regulated environment, training is a means to minimize (if not avoid) human error, a common cause of deviations and nonconformances. It’s no wonder that various standards and regulations, such as the following, require training as an integral part of the quality management system.

  • FDA 21 CFR Part 211.25 for pharmaceutical companies
  • FDA 21 CFR Part 820.25 for medical device manufacturers
  • ISO 9000 2000 for general manufacturers and other businesses
  • ISO 13485 for medical device manufacturers

Request Free!