Aim to Surpass Industry Standards
From the beginning Jamjoom Pharma was determined to create an advanced, future safe, manufacturing facility and to achieve superior standards by laying the foundation to meet and exceed where possible, cGMP (current Good Manufacturing Practice), US FDA, ISO 9000 and ISO 14001 (environmental) standards.
The state-of-the-art manufacturing facility of Jamjoom Pharma is in compliance with internationally recognized standards of current Good Manufacturing Practices (cGMP), and ensures that every product has the attributes of Safety, Purity, Identity, Quality and efficacy.
The teams of highly trained and qualified staff provide wealth of experience to ensure a high quality standards are maintained throughout the manufacturing process.
In the start up Phase 1 Lockwood Greene Inc., USA, were appointed as the technical consultants. Their close guidance and scrutiny ensured that the building design and layout, selection and installation of equipment, plant validation and other critical processes adhered to the most stringent of international pharmaceutical industry standards. The Phase 2 expansion commenced in 2011, CDI Life Sciences, USA, the internationally recognized Pharma consultants were appointed to ensure compliance with USFDA, EU and other stringent international standards.