We have partnered with some of the best WHO-GMP certified manufacturing units for all our manufacturing operations. We are well-equipped to provide multi-disciplinary pharmaceutical manufacturing for the mass production of tablets, capsules, syrups and injectables in both beta-lactam and non-beta lactam range. Besides, we also produce herbal products, ointments and other liquid formulations.

Our state-of-the-art manufacturing units have world-class infrastructure and facilities, equipment, tools and operations, the resultant of which is visible in the consistently high quality of our products. A wide range of packaging options enables us to select the best packaging that meets the product requirements to enable its protection throughout its shelf-life. We have Alu-Alu, Blister and Strip packing. We comply with all specifications starting from the purchase of raw material to the final dispatch of the finished goods.

Quality Assurance (QA) and Quality Control (QC):

We keep a check on the manufacturing operations through stringent routine checkups by various regulatory agencies and third-party audits. This assures us of the compliance to internationally recognized best manufacturing practices. Our assurance becomes the base and the trust for our business partners and also for the healthcare providers and the final consumers.

Our QA & QC department ensures that all current Good Manufacturing Practices (cGMP) are being followed during the formulation designing, development, manufacturing, packaging, storage and dispatch.

The Standard Operating Procedures (SOPs) have been fabricated for every single process from the start of the raw material procurement to the final formulation dispatch. Quality control is checked at every step throughout the production process. And, for the ingredients and formulations, guidelines recommended by the Good Laboratory Practices (GLP) are followed. Our partner companies comply with all these with the help of:

– Audits: Regular checks are done in the manufacturing, laboratory and other areas to check whether the SOPs are being followed and all the practices are in compliance with cGMP. Third parties are hired for audits so that there is no compromise with the quality. Audits are also done for facilities, equipment and systems and documentation is done for each process to ensure calibration and other malfunctioning do not come up.

– SOP Reviews: SOPs are reviewed from time to time and improved to enhance the efficiency and productivity of each procedure. Besides SOPs, manufacturing and analytical methodology; protocols and reports for the qualification & validation of processes are also periodically checked.

– In-process Quality Control (IPQC): These are the tests done during the production process at every stage. This minimizes deviations and errors. And whenever the problem is identified in between, the required corrective measures are adopted at the same time so that the final product is formulated as expected. Check-ups done at earlier stages when identified and corrected minimizes the probability of any compromise with the quality.

We have hired a highly skilled workforce to carry out all company operations and strive to lean the process with a focus on advancements and continual improvements.