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Liver Spheroids: A Major Step Towards Meaningful In Vitro Testing for Human Hepatotoxicity Potential

Article   Oct 31, 2018 | by Maureen Bunger, Product Manager for ADME-Tox Solutions, Lonza

Liver Spheroids:  A Major Step Towards Meaningful In Vitro Testing for Human Hepatotoxicity Potential


Testing Medicines After Brexit: Upholding High QC Standards for Pharmaceuticals


Maintaining robust quality control standards is a key priority for any commercial industry – but for pharmaceutical manufacturers, it can literally be a matter of life and death. The looming Brexit deadline is likely to be seen as a pivotal moment by those operating in the sector. The prospect of the UK leaving the European Union, and the jurisdiction of the EU’s unified single market for medicine regulation, is creating considerable uncertainty for drugmakers.


Helping the Pharmaceutical Industry Tackle the Evolving Challenge of Water Quality


Water plays a vital role in a broad range of processes within the pharmaceutical industry, from its use as a reagent and solvent in drug synthesis, to its utilization in formulation development and analytical testing, all the way through to product packaging and labeling. As a result, pharmaceutical companies must employ a range of treatment and monitoring processes to ensure the impurities present in water do not interfere with its intended use.


Standardization Challenges in Pharmaceutical Product Labeling


Product labels can be viewed as a “clinical instruction manual”, providing a concise description of the benefits and risks for a consumer and relevant information to dispensers, patients, and their caregivers. Here we take a look at labeling compliance, the importance of keeping information up-to-date, and risks associated with noncompliance.



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