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Process Validation Certificate QQI level 7 Course Launch

We are delighted to introduce our new programme: Certificate in Process Validation for Medical Device Manufacturing, a Level 7 programme accredited by Quality and Qualifications Ireland (QQI). This specialised course has been designed by John Lafferty, our Life Sciences Programme...

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How to Control Variation in Medical Device Manufacturing

By John Lafferty, Life Sciences Programme Director Read time: 9 minutes It all started with Big Bang, since then, the universe has been expanding and randomness (variation) has been increasing, humans try to put order on our world but we constantly have to battle against the for...

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Five New Life Sciences Courses Launched!

Here at SQT Training, we are delighted to announce that we have launched five new training courses! These courses have been developed in response to ongoing customer requests for these specific training topics. Visit our course pages below to see details of the course content. Al...

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How to Create a Risk Management Plan – Medical Device

Risk management standard ISO 14971:2019 has specific requirements for a Risk Management Plan. In order to comply with the standard, it is important that medical device manufacturers address these requirements in their own plans. In this blog, John Lafferty, our Life Sciences Prog...

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What are the top ten CAPA deficiencies?

John Lafferty, our Life Sciences Programme Director has compiled a list of the top ten CAPA deficiencies based on many years of working with Medical Device and Pharmaceutical manufacturing companies. Our CAPA training course will examine and demonstrate how to eliminate these d...

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