Manufacturing Facility
MANUFACTURING FACILITY
SIGMA PHARMA International (Pvt.) Ltd. manufacturing unit is designed to meet the highest standards of pharmaceutical production. Built in compliance with cGMP and DRAP regulations, the facility specializes in the manufacturing of tablets, capsules, sachets, oral dry powder suspensions, and creams/ointments/gels.Equipped with modern machinery, controlled production areas, and a robust HVAC system, the facility ensures product quality, safety, and consistency. Strict in-process controls, validated systems, and trained personnel guarantee that every batch meets regulatory and quality requirements.
Quality Control:
The Quality Control department has dedicated laboratories for chemical, instrumental, and microbiological testing, ensuring contamination-free operations. The department is equipped with advanced analytical instruments to enable precise and reliable testing of raw materials, in-process samples, and finished products. All testing procedures are carried out using validated methods under controlled environmental conditions to ensure product quality, safety, and regulatory compliance.
Quality Assurance:
The Quality Assurance department at Sigma Pharma ensures that every product consistently meets regulatory, safety, and quality standards through robust documentation, process validation, and continuous monitoring.
Regulatory Affairs:
At SIGMA PHARMA International (Pvt.) Ltd.., our Regulatory Affairs Department drives compliance excellence by aligning all products with the latest regulatory frameworks. From securing product approvals to maintaining certifications, this department ensures timely market access and regulatory integrity.
