Martin Gadsby, director at Optimal Industrial Technologies, looks at how Process Analytical Technology (PAT) can speed up the development and production of new and existing drugs.
In this thought leadership piece, Todd Mollner, global product owner, Respiratory Powders, GSK, tells use about the importance of powder testing in pharmaceutical manufacturing.
Peter Morgan - technical product specialist at Elementar UK - explains how TOC analysers help to deliver reliable results for drug makers, and how new advances are keeping them at the forefront of the quality assurance (QA) process.
In this online exclusive, Rina Nir, managing director of RadBee, looks at why Agile and DevOps are the ultimate cure for pharma companies’ ailing computer systems validation process.
In this article, Chris Maughan — managing director and Autoclave Validation SME at Thermal Compliance — investigates the use of wireless dataloggers for autoclave validation, looking into the how they can help and issues with their use.
Here, Jim Morris from NSF International, summarises the benefits of an excipient GMP certification programme (ECP) both from the point of view of the excipient manufacturer and the excipient customer.
The US Food and Drug Administration (FDA) has issued warnings to two Chinese drug manufacturers for violations of good manufacturing practice (GMP), according to a post from the Regulatory Affairs Professionals Society (RAPS).
In this interview with TraceLink’s Dan Walles, VP Global Solutions following his presentation at FutureLink Munich conference, we discuss automated software validation and how drug companies can benefit from it.
In this online exclusive, Graham Francis, product marketing manager at Kallik, explains how data integrity should be a top priority when using new technologies in the pharmaceutical industry.
In this article, Michael Avraam, global product manager at ChargePoint Technology discusses the potential issues with containment performance testing some techniques and developments that may help to ensure efficiency
Anton Paar understands your need for completely traceable results and supports you with a qualification and validation package following the 4Q model which fulfills the requirements of the pharmaceutical industry
