Challenges in filling for alum drug products: What does a CDMO need to successfully fill alum drug products?
What are Alum Products, and why are they challenging to fill? Alum products, commonly referring to aluminum-based adjuvants, play a…
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FSO vs FSP: One CRO highlights key considerations for your decision
The last decade has seen a significant increase in data-focused and online technologies used in clinical trials, adding to the…
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3 reasons why biotechs preparing for launch need a compliant content foundation
Industry data estimates that by 2026, first-time biotech launches will outnumber those from established companies by more than two to…
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The role of thin-layer chromatography (TLC) and high-performance liquid chromatography (HPLC) in modern pharmaceutical and herbal drug analysis
Introduction Chromatographic techniques are essential in pharmaceutical analysis, playing a critical role in quality control, authentication, and the standardisation of…
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Platform trials: The challenges, benefits, and best practices to maximize results with an EDC platform
As clinical research continues evolving to become more innovative and efficient, adaptive trials, specifically platform trials, are leading the charge.…
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Cell and gene therapy collections: The need for consistency
Cell and gene therapies (C>s) work by either introducing healthy cells into a patient's body (cell therapy) or by modifying…
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How bioconjugation is unlocking the next generation of drug development
Bioconjugation creates new molecules with increased stability and improved targeting. The process of joining proteins, peptides, or oligonucleotides to synthetic…
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Overcoming regulatory challenges in sterile manufacturing
In parenteral sterile fill-finish manufacturing, drug products must be free from viable microorganisms – critical for products administered via injection…
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Mastering compliance and copyright in healthcare and MedComms
In a recent webinar, Marc McArdle, CLA Customer Success Manager, was joined by Jackie Marchington, Head of Compliance and Ethics…
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How to manage regulatory complexities with clinical trial data
With the rise of electronic data capture (EDC) has come a raft of regulations on data use such as the…
