06.17.25 -- Understanding The Impact Of An RMP On Patient Risks Using Relational Risk Analysis

Investing in employee training and development is not just beneficial for the employees. It also contributes significantly to the organization’s success and competitive advantage.

Are robotic gloveless isolators the key to smarter, safer, scalable solutions? Discover how they can revolutionize aseptic filling by reducing contamination, minimizing waste, and enhancing flexibility.

Meeting the growing need for oligonucleotides means having the right tools. Examine the nine indispensable components, such as synthesis columns and C&D systems, for your facility.

Explore the development of high-quality, child-friendly oral formulations, as well as learn about new testing requirements for impurities and innovative approaches to creating age-appropriate medications.

Sterility is non-negotiable in pharmaceutical and medical device manufacturing. Uncover the top five sterilization challenges facing manufacturers today and the proven strategies to overcome them.

Although most legislation concerning the traceability of pharma products focuses on serialization rather than aggregation, the latter is an essential component of internal and external traceability of products.

Manufacturers generate vast amounts of data daily but struggle to make it actionable. Walk through these 10 steps and questionnaires to help you transform raw data into valuable insights.

Developing high-volume autoinjectors for concentrated drugs presents challenges in delivery, absorption, and patient usability raises concerns about their practicality and long-term effectiveness.

Isothermal Titration Calorimetry is a powerful technique for analyzing biochemical binding events, which is crucial for understanding molecular interactions and enzyme kinetics in biomedical research.

As molecular complexity continues to increase, flow chemistry is becoming an essential enabling technology to facilitate the integration of complex synthetic methods into API production.

Meeting the needs of the modern biomanufacturing landscape requires a combination of technology and digital solutions working together to effectively and efficiently meet your goals.

Find out how a platform integrating drug substance, drug product, and clinical testing within a single organization accelerates development and reduces costs, helping deliver positive outcomes earlier.

In analytical environments, precise weighing takes place inside containment where powders do not escape. Read on to examine the effectiveness of three vibration isolation strategies.

Partner with a right-sized CDMO to gain the agility, expertise, and personalized focus needed to accelerate your drug development with confidence.