Threading the Needle Between DIY and CDMO

Ravi Samavedam
Threading the Needle Between DIY and CDMO Teaser

In this BioPharm International article, you will learn why, in the common debate over building lab facilities versus outsourcing, the best strategy may be the middle ground: licensing.

The pharmaceutical industry continues to exponentially increase as new methods and technology become a launchpad for innovations, especially within the cell and gene therapy industry. According to a Pharmaceutical Research and Manufacturers of America (PhRMA) report (1), it takes, on average, 10–15 years and costs roughly $2.6 billion for a new drug to go from discovery to market. PhRMA also reported that 74% of clinical development are new approaches to treating disease across what is currently in the pipeline. Additionally, scientists and researchers are leaning toward a tailored approach to personalized medicine. FDA has predicted that by 2025 they will approve between 10–20 cell and gene therapy products per year (2).

Traditional ways of looking at the discovery and development of pharmaceutical and biopharmaceutical products, therapies, and treatments are not meeting the industry’s demand. As new approaches are being researched, conventional wisdom has forced biopharma companies to choose between two options in developing products: either build their own facilities, which can take years and cost millions, or outsource to contract manufacturing organizations (CMOs)/contract development and manufacturing organizations (CDMOs), which, especially in the wake of COVID-19, are facing years of backlogs.

To solve this manufacturer’s dilemma, companies are considering an innovative way to accelerate the development of pharmaceuticals and biotherapeutics—cleanroom licensing. Cleanroom licensing is a hybrid approach between do-it-yourself (DIY) and outsourcing to a CMO/CDMO that gives early phase or startup bio/pharma companies the opportunity to achieve their goals in a shorter timeframe than anticipated. This article will explore the benefits and challenges that companies, especially early startups, face in manufacturing and how cleanroom licensing puts them on the path from discovery to delivery.

Read the full article featured in the BioPharm International, Manufacturing and Facilities eBook 2022 or learn more about how Azzur's Cleanrooms on Demand™ cleanroom licensing model works.

Click Here to Read this article in the BioPharm International, Manufacturing and Facilities eBook 2022


  1. R. Samavedam, “Threading the Needle Between DIY and CDMO,” BioPharm International, Manufacturing and Facilities eBook 2022 (November 2022)

Ravi Samavedam Headshot

Ravi Samavedam

Ravi Samavedam joined Azzur Group in 2012 and is a Biochemical Engineer with more than 20 years of experience. Prior to his appointment to Chief Innovation Officer (CINO), Ravi served as President of Azzur Cleanrooms on Demand™ and previously was a General Manager of Azzur Boston. Ravi has been a part of technical operations, quality, and validation departments at some of the world’s foremost pharmaceutical manufacturers. He is an expert in phase-appropriate cGMP implementation, process validation, supplier management, and technology transfer. Ravi is an active member of industry and peer groups, and he is a frequent speaker at industry events.
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