1 Analysis of in-process, lot , finished product,samples.2 Reporting of results.3 Quick response to the production in terms of reports.4 Adherence to the GLP norms.5 Laboratory cleaning and maintenance. 6 Daily routine calibration in the 1st shift. 7 Particle size analysis as required.
The company was established way back in 1983 by Bhupinder Singh Manhas, the CMD of the company.
Manufacture and Exporter of Active Pharmaceutical ingredients.
Two manufacturing sites at Aurangabad and one at Vapi with capacity of 350,000 Litres.
Supply of API"s as a Major Thrust Area to pharma and generic companies.
Certificate of recognition as 'EXPORT HOUSE' by Government of India.
State-of-the art manufacturing facilities inspected & complying with cGMP norms as per USFDA, ICH Q7A, TGA, PIC, WHO-GMP, Schedule M and Japanese Foreign Accreditation.
State-of-the-art Quality Control Laboratories with GLP compliance.
cGMP compliance Pilot plant with clean room facility.
Powder processing area with pneumatic controls and Particle Size options: Milling & Micronising.
CRAMs offered.
State-of-the-art R & D center coming up 4th quarter 2013 in Navi-Mumbai.
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