12.11.25 -- Innovation, Growth (And Happiness) Projected For Pharma

There are two basic models of pharma manufacturing: batch and continuous. Here, we compare the two and examine the challenges they bring to containment product design.

Discover how CDMOs can modernize operations, safeguard data integrity, and improve audit readiness with practical strategies for connecting systems and reducing validation burdens.

Manual QbD methods slow timelines and increase risk. Learn how intelligent, digital frameworks are helping CMC teams improve quality, accelerate submissions, and meet rising regulatory expectations.

Navigating the inherent conflicts between GMP and biocontainment regulations is critical when designing specialized cleanrooms for advanced therapy manufacturing.

Find out more about a disposable pen for semaglutide designed for usability and compliance that supports accurate dosing and patient confidence while meeting regulatory standards.

Explore how orally disintegrating tablets act as a patient-centric solution to various factors that impact treatment adherence rates across various diseases.

Review the PDA Pharma Digitalization Survey and key challenges in pharmaceutical digitalization, including budget constraints, data security concerns, and resistance to change.

Begin your ADC manufacturing journey by finding a partner who can provide support through every phase of the conjugate life cycle, including process optimization, scale-up, and validation.

Pharma 4.0 offers a framework for digital transformation that emphasizes data integrity and connectivity. Uncover an agile approach to implement digital solutions for greater efficiency and compliance.

Among oral dosage forms, softgel capsules stand out as a versatile and high-performance option — offering superior delivery characteristics, consumer appeal, and brand differentiation.

Maintaining drug product sterility and compliance demands rigorous Container Closure Integrity (CCI) within contract manufacturing. Learn how to fortify your processes.

Sterile manufacturing remains vital, with resilient supply chains preventing shortages. Industry and regulators prioritize integrity as demand surges, making it the fastest-growing pharmaceutical segment.

The most common cause of downtime is the use of incorrect or out-of-date equipment. Examine considerations for improving your processes and increasing productivity.

Are you tired of the inefficiencies and gaps in your current process development methods? Say goodbye to manual documentation and hello to a revolutionary solution designed specifically for your needs.

A pharma company sought a CMO partner with commercial manufacturing capabilities and expertise as well as exemplary quality systems to find a cost-effective process to produce the API for a new drug.

Gain insight into how streamlined processes and collaboration enable faster, more reliable access to medicines for patients worldwide to help accelerate delivery and maintain quality.

Integration of robotics and automated systems across laboratory services significantly decreases experimental timelines, tightens precision, and enhances scientists' capacity for critical thinking.