


At Jedux Parenteral Pvt. Ltd., quality is not just a process—it is a core commitment. We strictly adhere to international pharmaceutical standards to ensure that every intravenous product we manufacture is safe, effective, and consistent.
Our Quality Control department is responsible for rigorous testing and verification of raw materials, in-process samples, and finished products. Every batch undergoes stringent analytical and microbiological testing before it is released.
State-of-the-art laboratories equipped with modern instrumentation (e.g., HPLC, IR, UV Spectrophotometers, pH meters, Polarimeter, Flame photometers, Particle Counters etc.)
Comprehensive testing protocols aligned with pharmacopeial standards (IP/BP/USP)
Environmental monitoring and sterility assurance for aseptic areas
Stability studies to ensure product efficacy throughout shelf life
Data integrity practices to ensure transparency and traceability

Our Quality Assurance system ensures that all processes, documentation, and operations comply with GMP (Good Manufacturing Practices) and regulatory standards. QA is involved at every stage—from sourcing materials to batch release and distribution. Core QA functions include:

Jedux Parenterals Pvt. Ltd. is committed to delivering world-class IV formulations with uncompromised quality. Through the integration of robust Quality Control and Quality Assurance systems, we ensure that each product that leaves our facility meets the highest standards of safety, sterility, and therapeutic value.
