Quality control is a key pharmaceutical business process. Our laboratory is a certified LPG laboratory and every individual who makes a product is committed to its quality. Quality control and assurance departments, such as Quality Control (QC) and Quality Assurance (QA), can examine the product for quality. Within the processing and packaging sectors, Quality Departments serve an auditing role.
We focus on and commit to products that meet international cGMP standards as an ethically binding policy for the long term. By providing a product with different quality parameters and within speculated delivery times, we strive continuously to achieve customer satisfaction. We anticipate and support the customer’s perspective in a timely manner with all the necessary technical data/information.
The Quality Control section uses precise analytical methods on a regular basis. For bioequivalence research, the laboratory is fully equipped with current and advanced instruments such as FTIR, TOC, and dissolution apparatus. Stability studies are carried out in accordance with current ICH recommendations.
We audit our numerous activities on a regular basis in order to make them more effective, relevant to the changing international level, and eco-friendly. We follow all applicable legal and regulatory obligations.
Our staff receives training on a regular basis, which develops team spirit while also educating them with the latest developments and advancements in the sector throughout the world.
We strictly adhere to the implementation of Quality Management Systems and are dedicated to making continuous improvements.
Our Quality Assurance Department is responsible for formulating and implementing quality systems. It also investigates shortcomings of the system and takes preventive and corrective actions as may be required. Quality Control department analysis APIs, excipients, primary & secondary packing materials, semi-finished & finished formulations, and water quality for the integrity of the final product. We have in-house Physico —Chemical, Instrumental & Microbiological testing labs equipped with state of the art instruments. To assure stability of the product stability studies are carried out on regular basis.
Under Quality Assurance and Quality Control department well qualified and experienced person takes care of regulatory work. We are capable of supporting the registration process and other regulatory documentation as per the needs of the concerned country. We support our associates by providing dossiers as per CTD, ACID, and specific country guidelines. We have several dossiers ready for fast pace product registration.
OFFICE ADD: Sub Plot No. 35, Swagat Industrial & Logistics Park, Mouje Dhanot, Ta. Kalol, Dist. Gandhinagar, Gujarat, India-382729