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Piramal Pharma Solutions Upgrades Oral Solid Dose Capabilities

New production block at Pithampur site increases total plant capacity to 4.5 billion doses.

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By: Tim Wright

Editor-in-Chief, Contract Pharma

Piramal Pharma Solutions, a contract development and manufacturing organization (CDMO), said a new production block has come online at the company’s drug product site in Pithampur, in the state of Madhya Pradesh, India. 

The new production area, known as V Block, can handle batch sizes of 150 to 600 kilograms, augmenting the site’s capacity to produce oral solid dosage form drug product. With the addition of V Block, the Pithampur site’s total production capacity increases from 3 billion doses to 4.5 billion doses. V Block includes aqueous and non-aqueous wet granulation (high shear, top spray and bottom spray); direct, mono, and bilayer compression; aqueous and non-aqueous coating; and bottle packaging technologies. Aggregation capabilities related to U.S. FDA e-pedigree and track and trace requirements are planned for V Block, as is the addition of dry granulation capabilities (roller compaction). Like the other four production blocks on site, V Block has dedicated personnel and material entry with biometric access control for the block and the operating cubicles within it, as well as dedicated air handling unit for each cubicle.

“The launch of this new large-scale production block represents a significant expansion of our ability to supply oral solid dosage form drug product to customers around the world,” said Peter DeYoung, CEO, Piramal Pharma Solutions. “This additional capacity further reiterates our commitment to being a patient-centric organization that’s focused on helping clients reduce the burden of disease on patients.”

The Pithampur site employs approximately 600 workers and supplies drug product to biotech, small pharma, large pharma, and large generics customers around the world, supporting their needs for both on-patent and generic drug projects. The site has been successfully inspected by a host of regulatory agencies including FDA (US), MHRA (UK), MPA (Sweden), TGA (Australia), FIMEA (Finland) and ANVISA (Brazil).


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