Latest Whitepapers

This whitepaper reviews the data integrity and computer system validation (CSV) regulatory landscape in the US and EU, identifies industry trends and challenges and offers best practices for maintaining compliance.

This whitepaper explores the regulatory environment surrounding data integrity, and what to look for in a laboratory information management system (LIMS) to ensure compliance.

This whitepaper explores the need for transparency between suppliers and manufacturers, ensuring the integrity of their products and maintaining trust among consumers and regulatory authorities alike.

As biopharmaceutical companies scale up manufacturing, many are turning to outsourcing for buffer and process liquid preparation. But before making this decision, organizations must carefully weigh up various factors, including manufacturing space, personnel requirements and analytical capabilities.

This article explores key challenges in vaccine development scale up and highlights various strategies for overcoming them.

This article explores major advances in disease modification for illnesses that still lack effective treatments, as well as some challenges and approaches to overcome them.

This whitepaper explores the latest advancements in OOC platforms that can help to efficiently simulate drug toxicity responses.

This article examines recent advancements in cell therapy research, from promising lab findings poised for clinical translation to enhancements in development, testing, and manufacturing processes.

Cell therapies, from regenerative medicine to immunotherapy, are transforming the medical landscape with 75 already approved globally and over 2,000 in development.

This article explores new workflows using data-driven modeling to improve culture medium and new control algorithms allowing for better modulation within the bioprocess design space.