Tip wear can lead to a host of issues for tablet design. Here, Bill Turner, technical service manager, tooling and tablets, and Kevin Queensen, technical service support tooling and tablets, Natoli Engineering, discuss the steps needed to avoid wear
With the end result of Brexit fast approaching, labelling supplier Kallik looks at the implications Brexit could place on labelling and compliance in the pharmaceutical sector.
In advance of new European measures to help reduce counterfeit medicines, Wayne Miller, healthcare director EMEA at Zebra Technologies, asks if the pharmaceutical supply chain is ready for true medicine traceability.
David O’Connell, director of scientific affairs at PCI Pharma Services, discusses the principles of roller compaction – particularly in the development and manufacturing of solid oral dosage forms containing highly potent active pharmaceutical ingred
With the potential of antimicrobial resistance (AMR) taking our modern medicine practices back to the stone age, governments around the world need to face the threat head on.
Stephen Tindal, director of science and technology at Catalent Pharma Solutions discusses what methods can be used to classify a drug’s solubility and bridge the divide between disciplines during development phases.
John Erdner, product manager, aseptic fill-finish systems, SP Scientific PennTech, discusses the advances being made in vial processing to help reduce the risk of vial damage and particle contamination.
Powder processing company Hanningfield details its recent case study for natural medicine company Integria Healthcare. Here, Hanningfield discusses how it helped Integria find a solution for sieving its dry powders
Jared Kimble, life sciences product specialist consultant at DXC Technology, writes about how regulatory intelligence can be utilised by life science companies.
From AI to mHealth, Jim Streeter, global vice president life sciences product strategy Oracle Health Sciences give us his pharma predictions for next year.
