Pagari Pharma is Quality Driven, US-based CDMO that offers concept to commericialization services that includes Research and Development, cGMP Laboratory Services, Technology Transfer & New Product Intorduction, and cGMP Manufacturing for Solid Oral Dosage form such as Tablets and Capsules and bottle filling.
Pagari Pharma is a newly built cGMP manufacturing facility that offers concept to commercialization of Finished Product Manufacturing.
We take our client, business, and quality seriously, we stage gate every step of the production process to deliver the highest-quality products.
From the selection of raw materials to the finished product, our process ensures precision, quality, and excellence.
End to End Service from Concept to Commercialization. Pagari Pharma is a full-service partner in developing, manufacturing, and packaging pharmaceutical needs. Service includes Prescription (Rx) and Over-the-counter pharmaceuticals. We pride ourselves in delivering the highest-quality products with client first motto.
At Pagari Pharma, we operate an ISO Class 8 certified cleanroom designed in accordance with ISO 14644-1 standards. This controlled environment is vital for minimizing contamination during critical pharmaceutical operations such as formulation, filling, and packaging. The cleanroom is continuously monitored for temperature, humidity, air pressure differentials, and particle levels to ensure full compliance with ISO and cGMP standards. Our commitment to maintaining strict environmental controls protects product integrity, ensures the safety of personnel, and meets regulatory expectations for high-quality pharmaceutical manufacturing.
Pagari Pharma implements a robust electronic Quality Management System (eQMS) that complies with FDA 21 CFR Part 11 requirements. This system upholds data integrity, security, and traceability across all quality-related processes in line with Good Manufacturing Practice (GMP). It digitally manages document control, audits, change control, CAPA, and training, enabling efficient, paperless operations with real-time visibility. Featuring validated workflows and secure electronic signatures, our eQMS enhances accountability, supports regulatory compliance, and ensures consistent oversight and continuous quality improvement throughout our operations.
At Pagari Pharma, we maintain comprehensive Quality Agreements with all contract manufacturers, suppliers, and third-party service providers involved in our supply chain. These agreements clearly define roles and responsibilities related to manufacturing, testing, packaging, documentation, audits, and regulatory compliance. Key areas include change control, deviation handling, product release, and communication protocols. By aligning external partners with our internal quality systems and FDA/cGMP requirements, we ensure consistency, transparency, and accountability—reducing risk and safeguarding product quality at every step of the process.
At Pagari Pharma, we operate an ISO Class 8 certified cleanroom designed in accordance with ISO 14644-1 standards. This controlled environment is vital for minimizing contamination during critical pharmaceutical operations such as formulation, filling, and packaging. The cleanroom is continuously monitored for temperature, humidity, air pressure differentials, and particle levels to ensure full compliance with ISO and cGMP standards. Our commitment to maintaining strict environmental controls protects product integrity, ensures the safety of personnel, and meets regulatory expectations for high-quality pharmaceutical manufacturing.
Pagari Pharma implements a robust electronic Quality Management System (eQMS) that complies with FDA 21 CFR Part 11 requirements. This system upholds data integrity, security, and traceability across all quality-related processes in line with Good Manufacturing Practice (GMP). It digitally manages document control, audits, change control, CAPA, and training, enabling efficient, paperless operations with real-time visibility. Featuring validated workflows and secure electronic signatures, our eQMS enhances accountability, supports regulatory compliance, and ensures consistent oversight and continuous quality improvement throughout our operations.
At Pagari Pharma, we maintain comprehensive Quality Agreements with all contract manufacturers, suppliers, and third-party service providers involved in our supply chain. These agreements clearly define roles and responsibilities related to manufacturing, testing, packaging, documentation, audits, and regulatory compliance. Key areas include change control, deviation handling, product release, and communication protocols. By aligning external partners with our internal quality systems and FDA/cGMP requirements, we ensure consistency, transparency, and accountability—reducing risk and safeguarding product quality at every step of the process.
At Pagari Pharma, we have embraced Soham ERP with PharmaCloud Services to strengthen our pharmaceutical operations. With this advanced digital solution, our processes across manufacturing, quality, compliance, exports, and sales are seamlessly integrated. This transformation enables real-time insights, paperless workflows, barcode traceability, and efficient management—ensuring we remain agile, compliant, and focused on delivering high-quality medicines with consistency and precision.
2+ Years Of Experience Pharmaceutical Industry
Nimish has completed Bussiness and Technology Management, Strategic Finance from NYU. Skilled Leader in finance function, Business Development, and risk management and Building strong team.
15+ Years Of Experience Pharmaceutical Industry
Mayur has Completed his Doctorate in Pharmaceutical Science from LIU, NY. Mayur bring expertise in Solid, & Liquid oral, and Parenteral dosage form. Skilled in Research and Development, Technology Transfer and Operations.
Reach out to us for any questions, concerns, or feedback. We’re here to assist you.
