Medical device Regulations (FAQs)
Medical device regulatory compliance FAQs: When is a product considered to be a medical device? What is meant by product classification system?
Medical device regulatory compliance FAQs: When is a product considered to be a medical device? What is meant by product classification system?
Medicine supply shortages relating to the pandemic continue to wreak havoc on treatment continuity. GMP education can help reduce shortages caused by …
Common reasons for medical device recalls Recalls related to software issues Software issues are the most common reason…
GMP Education Topic: Pharmaceutical Product Recalls Mock recalls help employees prepare for a recall. They also indicate to…
Bees on Cannabis & Hemp Crops: Good or bad…and do bees get high? Cannabis plants and insect (Honey…
Training & Development Topic: Upskilling (Life Sciences Industry). Why it pays to upskill and reskill employees rather than…
Are you an experienced trainer, but new to the Pharmaceutical industry and cGMP compliance training programs? Perhaps you…
Batch release decisions — and other product safety evaluations — rely on data integrity. In this pharmaceutical industry…
FDA Warning Letters for cGMP compliance issues relating to CAPAs If you’re a Pharmaceutical business owner or Quality…
Did you know you can mix and match GMP education topics when ordering online GMP training courses? You…
New training trends continue to emerge since Covid-19 was first recognised as a global threat. The 2021 Australian…
Online learning during the pandemic – a practical solution to GMP training requirements. The education industry was particularly…
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