12.04.24 -- UK To Implement Novel Framework For Point-Of-Care Manufacturing

Data center construction quality management is inadequate, with issues traced to human error. A stronger focus on quality control and assurance is needed for success.

Hear from a 21 CFR Part 11 expert supporting pharmaceutical, diagnostic, and medical device companies with implementing solutions and systems to ensure compliance.

Learn about the significance of residue removal, how it is effectively performed in cleanrooms to ensure the compliance of biosafety cabinets, and the impact of proper residue removal.

Explore common misconceptions that obstruct progress and why overcoming these barriers early provides a competitive edge when preparing for commercialization.

Listen as speakers discuss the regulatory landscape's impact on accelerating rare disease therapies, highlighting the role of surrogate endpoints in achieving better treatments and patient outcomes.

How do active purging pass-throughs offer a higher level of material control for cell and gene therapy facilities? Get the answer to this question and more, here.

Investigate the factors contributing to FDA recalls, the effects on both consumers and businesses, and how integrated digital solutions can play a crucial role in preventing such incidents.