04.08.25 -- Ensure Sterility Assurance With 11 Essential Factors

Explore five areas that can form part of a quality risk management strategy to ensure the compliant manufacturing of sterile drug products.

Engineering controls designed to mitigate exposure and create separation between the operator and toxic material are available in many forms, all with their own unique advantages and risks.

Discover the advantages of outsourcing equipment calibration to ISO 17025 accredited suppliers, which include cost efficiency and regulatory assurance. Read more to transform your calibration processes.

Numerous factors impact a drug safety program, but proper management of three key elements drives success while creating a scalable drug safety model.

Review advanced retrosynthetic analysis services and how these tools empower better, more efficient development of innovative small molecule drugs.

Understanding how a product influences microorganisms' resistance is crucial. Learn about relevant standards and references as well as recommendations for performing product D-value studies.

Examine how the biopharma industry leverages a platform to integrate, curate, and analyze diverse R&D data to enable collaborative, compliant, and AI-driven translational research.

Uncover how a CDMO automatically created a comprehensive batch report model to drive their reporting and speed root cause identification of quality failures with an Industrial DataOps software solution.

Automated manufacturing is a powerful but often misunderstood tool available to produce drug delivery and other pharmaceutical devices — whether established designs or innovative new ideas.

Find out more about a solution that ensures particularly efficient and reliable vertical and horizontal form fill and seal machine labeling.

Understand the importance of selecting the right container for sensitive drug products and how close collaboration is crucial for avoiding commercialization delays and safety risks to patients.

When selecting a chromatography resin, it is important to consider particle size, pore size, surface chemistry, scale, and surface area to help optimize efficiency, selectivity, and quality.