09.29.22 -- 6 Best Practices For Biopharma Talent Management In 2023

Multivariate analysis, which allows operators to model processes with several signals, can afford manufacturers a holistic, interconnected view of their operations in near real time.

As the field of biologics increases its focus on identifying new diseases to target and novel constructs to treat them, innovative administration devices are once again in the spotlight.

Employees must have the skills to effectively execute on process development and manufacturing operations. How do you ensure they are updated on complex bioprocessing techniques and technologies?

We provide an overview of the drug production life cycle, what happens at the preclinical stage, and review MES capabilities in the context of preclinical needs and priorities.

Discover how to simplify and manage the complexity of the inspection process easily, streamlining the inspection execution by making distressing inspection scenarios a thing of the past.

There are a variety of methods widely used in the detection of pinholes, cracks, and defective seals in containers, but a majority are destructive, causing the loss of product and packaging components.

Aseptic blow/fill/seal systems for packaging pharmaceutical liquids incorporate materials and processes that provide critical advantages for sustainable initiatives.

Throughout the pandemic, painkiller and sedative demands have spiked. Drug manufacturers and CDMOs have become critical in efforts to stabilize the supply of bupivacaine HCl and other essential drugs.

Learn how a drug developer collaborated to transform a generic solid active pharmaceutical ingredient (API) into a commercial, sterile injectable approved by regulators.

This tech company is expanding its current footprint in a bold bet on the enduring value of commercial real estate and the future of in-office work.

When vetting CDMOs for late-phase tech transfer, ensure success by partnering with a CMDO who has these five key attributes.

Realizing the potential of next-generation molecules calls on appropriate expression technologies and development processes that can facilitate their path to market.

This e-book offers an overview of clean containers and process requirements beyond sterility for professionals in quality departments, project managers, and procurement managers.

Faciliflex Express is designed for cell and gene therapy companies that need to rapidly bring their therapies to patients. The traditional process of specifying a cleanroom has thousands of decision points. Hear how Faciliflex Express eliminates the guesswork and provides a proven off-the-shelf solution.

Learn more about the best practice of leak testing of hermetically sealed devices in microelectronics, sensor technology, and other industries.