Newsletter | April 30, 2024

04.30.24 -- How To Design Highly Agile Biopharma Manufacturing Facilities

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Proactive Strategies To Evaluate And Mitigate Clinical Supply Risk

Successful clinical trials are crucial for advancing a novel therapeutic to market and maintaining a competitive edge. Clinical trials face risks such as supply shortages which can cause costly delays and impact the safety and well-being of the patients involved in the trial. Learn about strategies that can help build an understanding of risk assessment when developing a clinical supply plan with this on demand webinar.

FEATURED EDITORIAL

Designing Highly Agile Bio/Pharma Manufacturing Facilities

In bio/pharma, agile manufacturing is achieved through multipurpose designs that support a variety of unit operations manipulated and operated as independent yet connected modules. 

INDUSTRY INSIGHTS

RTSM Manages Clinical IP Dispensation In Schizophrenia Study

Challenged by the dispensation of an investigational product (IP) across diverse patient subgroups, see what solution this pharma was able to utilize to ensure optimal distribution and minimize wastage.

Build A Foundation For Successful Clinical Manufacturing

Establishing both the QTPP and CQA for your drug at the beginning of the product lifecycle is crucial for a successful GMP manufacturing process.

Logistics In Cell Therapy: Reducing Workflow Risk

Explore key steps that should be taken when executing a cell therapy clinical trial, from selecting the right sites to optimizing study retention.

Smart Packaging Advances The Quality Imperative In Clinical Trials

Learn how the right partner can help seamlessly integrate smart packaging and move toward an enhanced, patient-centric trial experience, ensuring that study protocols are not compromised.

SOLUTIONS

The Ultimate Guide To Clinical Supplies For Japan Studies

Using IRT Data To Automate And Optimize Clinical Supply

Aseptic Manufacturing Services