03.08.24 -- Assessing Cross Contamination Using Layers Of Protection Analysis

The COVID-19 crisis acted as a catalyst for digital transformation in the healthcare industry. Learn how this transformation has impacted trends and new possibilities in the life sciences sector.

Explore a comprehensive guide to choosing the right stereo microscope for your application, including the crucial factors you should consider and analyze.

The development of physically stable, biologically active dry powder formulations of large molecules for inhalation has remained a challenge.

Industry experts discuss the recently revised Annex 1, including the concept of a contamination control strategy and what contamination controls mean when they work together to provide an answer.

Find out how to face the challenges in tablet manufacturing environments through supportive vendor partnerships.

Ultimately, to serve the highly competitive biopharma and pharmaceutical markets, CDMOs must be adaptable to the culture of the company for which they are working.

Explore the results of a unique comparative study of CCIT and find a suitable deterministic test method to replace the blue dye test that follows the latest guidelines.

The content and creation of blinded labels are tightly regulated and benefit from the guidance of an experienced partner.

Nasal spray administration of medicine offers advantages over oral and IV delivery. Experts discuss the advantages and opportunities of adopting unit- and bi-dose nasal delivery technology.

Explore the advantages and challenges of continuous flow processes and the concept of mini-monoplant technology, along with examples that demonstrate the versatility of continuous processing.

We present a simple protocol for scaling up AAV production using HEK293 host cells cultured in suspension and under serum-free conditions.

Choosing a custom cell culture media formulation can improve your biopharma manufacturing process performance, and working with media development collaborators can help you navigate that process.

Commissioning is the systemic and documented approach to verify that your cleanroom performs as designed and in accordance with your manufacturing needs.