Manufacturing Excellence
Our quality commitment is not a marketing statement — it is a system of processes, standards, and people that ensures every product is safe, effective, and consistently excellent.
Our Quality Philosophy
At Lucid Pharmatech, quality is built into our products — not tested into them. This distinction is fundamental. We implement Quality by Design (QbD) principles, ensuring that quality considerations are embedded at every stage of product development and manufacturing, rather than being an afterthought at the end of production.
GMP-Aligned Manufacturing
All manufacturing operations at Lucid Pharmatech are aligned with Good Manufacturing Practice (GMP) guidelines. Our processes are designed to minimize risk, prevent contamination, and ensure batch-to-batch consistency across all product lines.
- Rigorous raw material qualification and testing
- Controlled manufacturing environments with environmental monitoring
- Comprehensive in-process controls and checkpoints
- Final product testing against established specifications
- Stability programs to validate product shelf life
Quality Control Systems
Our Quality Control function operates independently from manufacturing, ensuring objective evaluation of all products. We maintain comprehensive documentation, traceability records, and deviation management systems that enable us to identify, investigate, and resolve quality issues promptly and transparently.
Continuous Improvement
We are committed to ongoing improvement of our quality systems through regular internal audits, training programs, and adoption of evolving pharmaceutical best practices. Our quality team stays current with regulatory guidelines from major authorities including the CDSCO and internationally recognized standards.
Packaging Quality
Quality extends to our packaging. We ensure all primary and secondary packaging materials are qualified, tested, and compatible with our pharmaceutical formulations — protecting product integrity from manufacturing through to the patient.