The forthcoming ISO IDMP standards governing
pharmaceutical product information recording have
far-reaching implications for the way companies capture,
collate, organise and report a very wide range of operational
data. Master data management as an approach offers an
efficient, definitive way to cope with this. Sonia Monahan
of AMPLEXOR International explains in her article how
companies can ensure they derive maximum payback from
any new system investments.
Current Edition
Current Edition
Subsection - CDMO
Examining how innovative technologies, integrated manufacturing approaches and AI are shaping manufacturing.
Continue readingSubsection - Injectables
Exploring advances in injectable drug delivery and sterile manufacturing, designed to improve patient-centric delivery.
Continue readingSubsection - Neurodegenerative Diseases
Exploring emerging approaches to neurodegenerative disease research and treatment.
Continue readingSubsection - Nasal & Pulmonary
Highlighting how advances in nasal and pulmonary drug delivery, formulation, devices and analytics are enabling more complex therapies.
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Preparing for IDMP: The Latest Advice on How to Ensure a Smooth Transition
