05.01.25 -- Retrofitting Facilities For Modern Bioprocessing And Pharma Production

Asian pharma manufacturers are constantly under pressure to produce high-quality products on time. Explore how Asian pharmaceutical companies are leveraging MES to enhance efficiency.

Discover general cleaning concepts, important sanitary surface considerations, cleaning guidelines for cannabis manufacturers, medical device re-processing and cleaning applications, and more.

When choosing a CDMO partner, it is essential to prioritize quality. Examine how the right partner can instill confidence in the safety and effectiveness of your pharmaceutical products.

Learn how transparency and disclosure ensure that clinical data is accessible to the public and regulatory bodies in medical writing, which helps foster trust and accountability.

As demand for capabilities and resources grows throughout a project, both become strained in-house and the scale-up process becomes a steeper hill to climb.

The rising incidence and severity of obesity have amplified a therapeutic need in healthcare. Read more about Dr. Srinivasan Shanmugam discussing the challenges and impact of GLP-1 analogs.

To help manage impurities and mitigate risk across all stages of development, consider the benefits of working with a CDMO that has robust chemistry understanding and manufacturing experience.

Gain insight into how a global leader in pharmaceutical manufacturing overcame significant challenges related to their ultrafiltration process.

Technical transfers are one of the most critical, yet challenging steps in drug development; therefore, an effective strategy is essential to accelerate the translation of projects from bench to market.