10.29.26 -- Capturing Tablet Disintegration For Improved OSD Development

Discover essential analytical techniques in biotherapeutics development, as well as ITC, DSC, and Rheology—powerful tools for understanding formulation, stability, and efficacy in drug development.

Tight timelines and coordinated packaging execution drove a high-stakes product launch ahead of a national competitor, ultimately capturing over half the market and setting a new benchmark.

David Lyon, Ph.D., and Molly Adam answer attendee questions from a recent webinar about three enabling technologies designed to improve drug solubility in organic solvents for spray drying.

Packaging must evolve alongside drug development to ensure stability, safety, and regulatory adherence, utilizing innovative designs to improve therapeutic outcomes and patient accessibility.

Accelerate intact mass analysis of GLP-1 analogues with automated purity calculations, sub-ppm mass accuracy, and impurity detection for consistent results in under one minute per sample.

Incorporating phase-specific quality standards ensures GMP compliance. Collaborating with an experienced CDMO addresses late-stage quality needs and efficiently manages development timelines.

Facility shutdowns often compromise contamination control strategies. Transitioning from manual cleaning to automated bio-decontamination ensures a more effective facility restart, eliminating risks.

Safeguarding drug quality requires robust stability testing, yet legacy systems often hinder compliance. See how modern digital workflows eliminate manual errors and streamline study management.

The pre-filled syringe space is one of the fastest growing sectors, offering greater patient safety and lower costs. But pre-filled doesn’t translate to easily filled; there are obstacles.

An experienced industry leader shares insights on how biosimilars are reshaping healthcare through scale, manufacturing discipline, supply reliability, and long‑term commercial strategy.

What is actually behind the procurement of a pharmaceutical labeling machine and how does the process work? You can find out here what the path to your pharmaceutical labeling machine looks like.

Building redundancy into testing helps avoid delays and supply risks. Qualified third-party labs provide flexible capacity, smooth transfers, and reliable batch release.

Selecting the right isolator for aseptic filling requires more than comparing features. Explore essential questions to ask and make informed decisions that align with your process and operational goals.

Routine trend analysis of total and viable particle monitoring data helps identify operational shifts early, set statistical limits, and strengthen cleanroom contamination control strategies.

Catalyst selection is vital for green chemistry. Balancing efficiency and environmental impact requires smart decisions to advance sustainable synthetic methods without losing performance.

Risk assessment is integral to manufacturing processes, particularly in drug production, and having effective containment strategies can help identify potential hazards and ensure worker safety.