Download this whitepaper to discover the latest developments and research in QA/QC for biologic therapies via exclusive articles, interviews and application notes.
Fact: the number of biologics on the market is growing.
This report addresses the key factors shaping pharmaceutical formulation, including regulation, QC and analysis.
Access the full report now to discover the techniques, tools and innovations that are transforming pharmaceutical formulation, and learn how to position your organisation for long-term success.
What you’ll discover:
Key trends shaping the pharmaceutical formulation sector
Innovations leading progress in pharmaceutical formulation and how senior professionals can harness their benefits
Considerations and best practices when utilising QbD during formulation of oral solid dosage forms
Can’t attend live? No worries – register to receive the recording post-event.
The precision, customisation and potential to combat or cure previously untreatable diseases makes biological products such as cell and gene therapies extremely desirable and, as a result, it has never been more essential for QA/QC professionals to rise to the challenge of complex biological therapies.
In the original pieces listed below, experts from across the biopharmaceutical industry discuss the technologies making the adoption of high quality, consistent and safe biological therapies a possibility, exploring everything from how to combat contamination in sterile products to specific analytical techniques.
Included in this whitepaper:
O-glycan analysis of therapeutic proteins enabled by O-glycoprotease
Xiaofeng Shi, Saulius Vainauskas and Christopher H Taron, New England Biolabs (NEB)
Optimising analytical separations of synthetic RNA with modified HPLC
Anastassia Kanavarioti, Yenos Analytical LLC, and Sandra Rontree, Thermo Fisher Scientific
Release of sterile medicinal products – looking at the focal points
Tim Sandle, Bio Products Laboratory
Preventing contamination during biopharmaceutical production
Victoria Rees, European Pharmaceutical Review
Native liquid chromatography coupled to mass spectrometric analysis for the assessment of higher order structures of proteins
Dr Ioannis A Papayannopoulos, Celldex Therapeutics
Application of liquid chromatography in characterisation of lipid nanoparticle-based oligonucleotides
Adam Socia, Andreas Abend, Yong Liu and Yuejie Zhao, MSD
Assessing host cell protein contamination in biotechnological products
Vanda Dolabela de Magalhães, Bionovis
Solid- and Liquid-State NMR for monitoring of polysaccharide antigen in the manufacturing process
Francesco Berti, GSK Vaccines
Innovations in analytical science: development of rapid, highthroughput glycoanalytics for biopharmaceuticals
Victoria Smith, Lewis Wharram and Stuart Jamieson, CPI Biologics
Download the whitepaper for all this and more!
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