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Technical Capabilities and Expertise Assess specific filling line capabilities (vials, syringes, cartridges) Evaluate their experience with different container closure systems Review their lyophilization capabilities and capacity if required Examine their filter validation expertise and approach Assess their component preparation and sterilization processes Review their visual inspection capabilities (manual and automated) Verify their analytical testing capabilities for sterile products In the latest Pharma Source Podcast Carole Delauney warns that sterile injectable manufacturing is not just fill-finisha misconception that can cost biotech companies millions and even derail entire drug development programs

He considers it a potent biohack and a tool he may use again, but hes keen to see more scientific research

"This is something that Indian generic players have been preparing for a very long time," Salil Kallianpur, an independent pharma consultant based in India, told CNBC

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