White Paper Library

Download our white paper to understand how toxicological assessment supports the evaluation and control of drug impurities across pharmaceutical development.

Download our white paper to understand how chemical characterization and toxicological risk assessment support biological evaluation and regulatory compliance for medical devices.

Download our case study to see how a novel RSV-A challenge agent was clinically validated in a controlled human infection model, generating early human efficacy data for RSV vaccine and antiviral development.

We explore various aspects of food packaging and the importance of standards and certification.

Explore clinical safety testing strategies that ensure cosmetic and cosmeceutical products can be tolerated by rosacea-prone skin and meet National Rosacea Society expectations.

We discuss the key points of an integrated management system (IMS) for the food sector.

Download our white paper to understand how USP <665> supports risk-based extractables and leachables assessment for single-use systems in pharmaceutical manufacturing.

A technical overview of the RSV-NICA controlled human infection model, including its GMP manufacturing, clinical validation with 100% infection rate, and how it enables faster early efficacy assessment for RSV programs.

Download our white paper to understand the latest changes in Australia’s 2025 Spectrum Plan and how they shape regulation, innovation and industry development.

Download our latest white paper to understand how artificial intelligence is reshaping cybersecurity and data privacy – and what you can do to protect your organization.