To ensure the highest grade of quality standard we have adopted Quality Management Systems. The quality process begins from sourcing the highest grade of raw materials from certified vendors in the industry to storing them in facilities that are built according to the industry and regulatory norms.

We have state of the art machines that are involved in the production process. The machines are routinely checked and
maintained to ensure consistent production without any hindrances.

We have clean rooms for final processing of the material. We have adopted packaging techniques that ensure our product is contained within the clean room environment.

In addition to production, we also follow strict documentation standards to track all actions and processes. The collected data is systematically recorded and helps for batch tracking, quality monitoring and standardised manufacturing practices. In today's data-driven world, information guides us to innovate and enhance production processes. We keep quality documentation in accordance with FDA and GMP norms.

A few documents available with us for all our products.

• Process Validation
• Analytical Method Validation
• Batch Manufacturing Records
• Standard Operating Procedures
• Equipment Qualifications
• Stability Study of Products
• Cleaning Validation
• Drug Manufacturing File (DMF)

Apart from our Quality management system we have rigorous training of our staff to keep them updated with the current and modern practices in the industry. We believe in an inclusive culture hence we take suggestions from them in training sessions and our routine meetings. Because of this culture the most unique and effective solutions are developed by our team members. We are a company dedicated to achieving excellence in every stage of the process. We constantly strive to improve our production and research to enhance our capabilities. This growth in competence is reflected in the superior products we deliver to our customers.