12.13.24 -- The Building Blocks For Successful CDMO–Pharma Relationships For Packaging Operations

Companies aiming to accelerate biomanufacturing operations and use resources efficiently need access to technologies that can safely and efficiently complete their workflow from idea to injection.

Learn in detail about High Voltage Leak Detection (HVLD), packaging applications that can be inspected with HVLD, and how to determine the best leak-testing method for your application.

Get updated on recent advances in metabolome analysis by mass spectrometry with this introduction to the different approaches and technologies.

To ensure the safety of personnel throughout the production of HPAPIs, manufacturers must effectively utilize containment and well-designed equipment.

Effective procedure development starts with understanding the purpose and should integrate change management, risk management, and knowledge management to ensure a robust quality system.

See how applying lyophilization-based micronization methodology at a small scale helps to support challenging formulation development projects.

Here, we discuss the challenges and solutions for cell and gene therapies, focusing on performance, scalability, and regulatory compliance to accelerate commercialization and improve patient access.

Learn about the rising demand for cleanrooms in the biopharmaceutical industry, factors driving cleanroom design, building in flexibility, the role of critical path assessments, and more.

Today's quality control (QC) labs need instruments that can accurately take on a wide range of tasks. Discover a system that allows QC labs to enhance their capabilities and achieve various goals.

Review the key trends and challenges shaping the CDMO industry as well as the tools helping a leading CDMO meet the growing demand for pediatric formulations and taste-masking solutions.

Dr. Ian Lafferty, Chief Technical Officer at Upperton shares valuable insights on transforming spray-dried dispersions into effective tablet formulations.

Gain expert insights into how to develop a spray-dried powder formulation and scale it from early feasibility studies to commercial manufacturing.

The demand for high-concentration/subcutaneous drugs is on the rise. Explore opportunities for enhancing your biotech drug production platform.

DFM discussion must be concise and backed by both historical data and up-to-the-minute insights, e.g., discovered through prototyping, test runs, etc.

Discover how a CDMO's mounting challenges with manual product quality review (PQR) processes were resolved through the implementation of a next-generation cloud-based solution.

Achieving precise measurements in a high-throughput setting can be challenging without disrupting workflows or deadlines. Learn about a new tool for rapid biotherapeutic thermal stability characterization.

Gain the knowledge and tools necessary to facilitate successful technology transfer and accelerate the translation of your projects from bench to market.

Experts discuss the best time to start thinking about patient-centricity, the steps developers can take to achieve patient-centric drug design, and how formulation and dosage forms can make a difference.