The future of pharma & medical device manufacturing is already here, and what’s not here yet is rapidly unfolding. There’s a lot to take in this year in terms of industry trends, new technologies, and GxP & GMP compliance guidelines for pharmaceutical and medical device organisations! It would be nice if the latest AI technologies…
The 2024 Pharma & Device Forum was held on May 23-24 at the Melbourne Convention & Exhibition Centre (MCEC) in Victoria, Australia. This was an important gathering of pharmaceutical manufacturing and medical device industry professionals including business owners, quality managers, operations experts, product developers and cleanroom engineers. This is a “for industry, by industry” life…
When budgeting for personnel to attend conferences and networking events, decision-makers often prioritise costs and potential downtime over the long-term benefits. However, investing in professional development (PD) opportunities for life science professionals can lead to significant productivity gains and financial returns. Professional Development is best viewed as an ‘uptime’ opportunity vs a ‘downtime’ event. That’s…
Modernization of Cosmetics Regulation Act (MoCRA) – Part 1 of 2 resource articles. This article introduces US FDA regulations for cosmetic products. Modernization of Cosmetics Regulation Act (MoCRA) of 2022 Cosmetic Manufacturing Regulatory Compliance On December 29, 2022, the FD&C Act was updated with the passing of the Modernization of Cosmetics Regulation Act (MoCRA) of…
The time has come for us to talk about the Data Integrity elephant in the GMP room. Despite Data Integrity being a hot topic in industry for the past 5 years, it continues to attract a lot of attention – the constant discussion generating more questions than answers, and creating confusion over what does and…
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