According to Jeff Gust, Chief Corporate Metrologist at Fluke Corp, the main issue with conformity statements is that measurements are just estimates of the true value.
According to APQC's blog post by Grace Duffy, organizational maturity reflects an organization’s ability to adapt, innovate, and efficiently meet customer needs.
When launching Greenfield projects in the pharmaceutical or medical device industries, businesses often face the decision between Good Manufacturing Practice (GMP) licensing and ISO 13485 accreditation.
Identifying and controlling Critical Process Parameters (CPPs) is essential to maintaining quality and consistency in medical and pharmaceutical industries, according to Quality Systems Now's blog post.
Implementing an electronic quality management system (eQMS) offers a lot of potential for improving processes, according to Quality Systems Now's commentary.
Dr. Murugan Kandasamy, Managing Director & CEO at DQS India, Head - Medical Global Support Center, has published a new blog post about Classification of Medical Devices under EU MDR. The most important issues he discusses are:
A commentary by Michael Dunst and Dietmar Vahs points out that the famed "Made in Germany" label is losing some of its sparkle as more German companies consider moving their operations abroad.
Michael Mills writes how Dr. Yvonne Simmons Howze highlights that quality stems from personal excellence, urging individuals to embrace the "Five C's" to overcome internal workplace threats.