Simpex pharma Pvt. Ltd. committed to providing paramount customer satisfaction through quality and timely delivery. We are dedicated for successful collaboration with internal and external customers to ensure integration of best practices and quality processes that are developed, maintained and being improved continuously.
We strive to identify, meet and exceed our customer’s quality requirements through good manufacturing practices. We followed regularly updated national and international standards i.e. Schedule-M, 21CFR regulation pertaining to country specific regulatory norms as per registered product to maintain safety, ef?cacy, identity, strength and purity of our products. We are committed to add value for our customers with continuous improvements and innovations.
Quality systems and SOPs such as Change Controls, Deviations, Customer Complaint, Product Recall, CAPA, Internal Audit and OOS are controlled by EQMS.
Compliant with the WHO-TRS, Schedule-M are compliance for pharmaceutical requirements, pharmacopeias such as USP, EP, BP, JP, IP etc.
All equipment and utilities are qualified and Process & Cleaning validation, HACCP activities are performed as per Validation Master Plan.