09.28.22 -- Cleanroom Project Design, Delivery, And Construction Best Practices

As the life sciences industry responds to the COVID-19 pandemic in record fashion, cleanroom technologies have proven vital to efforts to combat the pandemic. A new streamlined process delivers complete custom cleanrooms from scratch in as little as four months from concept initiation.

Many of today’s most advanced therapeutic molecules are parenteral, administered via injection or infusion and dispensed by healthcare providers around the world. Developed with standard factory fabricated modular components, cleanroom systems are purposely designed to simplify implementation of the aseptic manufacturing space that the industry needs to meet future sterile injectable capacity demand.

Commissioning is the systemic and documented approach to verify that your cleanroom performs as designed and in accordance with your manufacturing needs. Read how a proven modular design plus an experienced installation team plus GDP equals a risk-free commissioning process.

Maintaining FDA compliance is essential to your business operations, and downtime of any sort could derail your business and potentially harm patients. A cleanroom facility that remains safe for your workers — and where the therapeutics they produce remain safe for patients — can ease your compliance concerns.

Current advances in cell, gene, and tissue therapies require a rethinking of how — and where — cleanroom manufacturing facilities could be built to enable more options for sponsor process control. We share what factors are central to successful entry into commercialization of new therapeutic production capital projects.