Pharma & Device Forum – Education Sessions On the 31st of March and 1st of April 2025, ~ 250 life science professionals, including those from the pharmaceutical industry, laboratory sciences/research sectors, quality management, operations management, and medical devices sectors, came together in Melbourne for the 14th ‘GMP Forum’ (the 2025 Pharma & Device Forum organised…
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…
The definition of technology transfer (TT) may vary depending on the type of TT. It is generally referred as bridge between academia and industry, though it may also involve transfer of knowledge within the industry. In the pharmaceutical industry, TT would very often include transfer of new product and process from development to manufacturing. It…
The pharmaceutical sector in Vietnam has witnessed substantial growth and transformations in the past two decades. Government health policies have played a pivotal role in accelerating the development of Vietnam’s pharmaceutical industry, leading to a significant increase in its market size—from USD 5.4 billion in 2018 to an estimated USD 6.5 billion in 2021. According…
In a world where technology is advancing at an unprecedented pace, the integration of digital health technologies into the healthcare landscape has become increasingly vital. Recognizing the significance of this convergence, the U.S. Food and Drug Administration (FDA) has taken a significant step forward this month (October 2023) by establishing a new Advisory Committee on…
Navigating the Latest TGA Amendments: Essential Information for Class IIa & Class IIb Medical Device Listings Ever since the shakeup of the European Union (EU) Medical Device Regulations (MDR) in 2017, the Therapeutic Goods Administration (TGA) have adjusted their dependence on utilising the EU as their basis for listing on the Australian Register of Therapeutic…
We are proud to say that PharmOut is now a carbon neutral practice, in doing so reaffirming our commitment as a sustainable global consultancy practice. As a means of continuous improvement, this continues to prepare us for the challenges that face us in the responsible design and operation of buildings in working to reduce carbon…
FDA Citation Tracking Tool Updated I’m excited to share that QikSolve has helped us to update track and trend all the FDA inspection 483 citations from 2011 to current months. This tool dynamically scrapes data from various live websites and databases and provides a single, secure portal which to track and trend data, or rather…
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