About Us
Company Overview
- 20000 sq. feet production block facility to comply audit for advanced intermediate manufacturing block with good ventilation condition.
- 2000 sq. feet Separate quality control department to perform in house testing materials.
- 5000 sq feet separate raw material storage area to avoid cross contaminations.
- 3000 sq feet separate utility area to maintain hygienic condition.
- Equipment’s installed to perform multiple types of reactions.
- Exclusion of steroids, cytotoxic, herbicides and veterinary related products in same production block.
- 100% power back up system.
- Zero discharged MEE system with 7 KL/Day capacity.data
Our Expertise
Quality Assurance
- Our systems and procedures adhere to international regulatory guidelines, ensuring a high standard of quality.
- Written procedures and in line documentation with controlled by Quality assurance team.
- We guarantee adherence to our quality policy through process monitoring, corrective and preventive actions and change management system.
- Through continuous training and quality risk management,improvement in process performance and product quality.
Quality Control
- State of the art laboratory facility with separate physical testing and instrumental testing lab.
- In-house HPLC, GC system and other testing
instruments like Karl Fischer, auto titrator, pH meter, analytical balance, are connected with compliance system. - Rigorous testing of raw material, in process samples, intermediates and final products before dispatch.
- Conducting hold time study and retain samples of intermediates as per global and regulatory requirements.
Product Development
- Our capabilities span gm scale to commercial scale synthesis of Advanced intermediates
- dedicated R & D experts with more than 15 year experience in Reputed pharmaceutical companies to develop and commercialize new products .
- In house R & D lab and Scale up facility to commercialese product.