02.21.25 -- Are Plant-Based APIs The Future Of Pharma And Nutraceuticals?

During early-stage development, utilize the key considerations outlined here to avoid common pitfalls and expedite the transition from molecule to market.

Delve into why cleanroom systems are purposely designed to simplify the implementation of the aseptic manufacturing space that the industry needs to meet future sterile injectable capacity demand.

Leveraging computer-aided synthesis design technology and route scouting in the early stages of development can aid you in designing an efficient and cost-effective path to API manufacturing.

Explore the digital evolution of manufacturing control and management, the building blocks of Pharma 4.0, and how the life sciences industry can realize the full potential of Pharma 4.0.

Utilizing tape for positioning during Sterilize in Place (SIP) validation can introduce numerous issues. Review the top eight reasons why tape should be avoided during SIP validation cycles.

Learn how two recent initiatives from the FDA and PDA are paving the way for the compliant and practical implementation of AI into pharmaceutical manufacturing.

By performing stability storage in-house, you are taking on several risks. Find out how you can eliminate stability storage risks and save your resources and finances.

With a growing interest in developing new and improved bioconjugate drugs, explore an “innovation through collaboration” approach that can facilitate access to next-generation conjugation technologies.

Gain insights into Annex 1 updates on contamination control in pharmaceutical cleanrooms, emphasizing cleaning consistency, training, advanced tools, and technologies to achieve regulatory compliance.

Unlock the potential of nasal inhalation for delivering active pharmaceutical ingredients by evaluating the advantages of both liquid and dry powder formulations as companies innovate a variety of therapies.

Leverage advanced elemental impurity testing methods to ensure the safety, compliance, and accuracy of your drug products throughout the manufacturing process.

Explore key considerations for ensuring accuracy and efficiency in your process, from robust control systems to diverse printing options and comprehensive qualifications.

Learn about a flexible aseptic processing system that provides modular, semi-automated, and fully automated solutions to meet demands at all stages of development.