Case study: Fully automated packaging line with track and trace solution
Read the success story of a Polish pharma manufacturer that ensured its production with a fully automated packaging line with track and trace solution.
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Read the success story of a Polish pharma manufacturer that ensured its production with a fully automated packaging line with track and trace solution.
Save time with the feedback control option at the Crystal16 and the CrystalBreeder. Simplify crystallisation by automating your process.
Without confidence in your environmental monitoring (EM) data and microbiological testing, you can never be completely sure that your products are free from unwanted microorganisms. Our Accugenix® microbial identification and strain typing services offer unparalleled accuracy that you can rely on.
Case study example regarding finding impurities and controlling formations at release.
Overview of Adare Pharma Solutions- a leading global CDMO with innovative oral dose technology platforms.
Continuous wet granulation and drying have long been a hot topic in pharmaceutical manufacturing. The QbCon® 1 system solves all existing problems.
The journey from large molecule to approved biotherapeutic is long, costly, complex, and fraught with risk – yet rewards for success are substantial.
This paper takes a closer look at plastic storage bags for bioprocesses focusing on a shift from multilayer to single-layer storage solutions.
A framework to enable a holistic approach to CCI that assures both primary packaging and process contribute to good CCI of sterile vial product.
This whitepaper considers the latest EU GMP Annex 1 draft and its impact on the control and release of sterile products.
Replacing traditional moisture analysis methods with a rapid, analytical and non-destructive method to improve the quality of freeze-dried product.
A fast, high-resolution, and reproducible reverse phase HPLC method using the BIOshell™ A400 Protein C4 column to analyse the intact mAb Trastuzumab.
What is dissolution testing, why is it critical, what to consider for your method validation? Learn more in this quick guide.
Recent technological advances have made it easier to cope with the complexity of mass spectrometry (MS) based glycan analysis.
Key requirements to ensure patient safety in the present-day development and production of viral vaccines, and the challenges going forward.