Robust Product Development and Manufacturing Processes

The R&D department involves designing and optimizing new formulations, selecting suitable raw materials, and establishing robust manufacturing processes. The R&D team validates the analytical method for raw materials & finished products. The team conducts trials, analytical testing, and stability studies to ensure the product meets quality, safety, and regulatory standards before it moves to commercial production.

Active Pharmaceutical Ingredients (APIs), excipients, and packaging materials undergo rigorous inspection in accordance with our Standard Operating Procedures (SOPs) and are immediately placed under quarantine. The Quality Control (QC) department conducts identification, potency determination, and other required analyses as per compendia & approved STP. Only materials that meet all specifications are approved, labeled accordingly, and carefully transferred to designated, controlled storage areas. QC also actively manages retest schedules to ensure ongoing compliance and quality of materials.

We manufactured various dosage forms such as tablet, capsule, powder for suspension, oral liquid, topical preparation, cream, ointment, and injection using leading-edge technology and modern machinery. We follow validated processes and maintain the clean room as required for different dosage forms. In-process quality is continuously monitored and ensured by the Quality Assurance (QA) department at every stage of the manufacturing process. We strictly adhere to GMP throughout the entire manufacturing process to ensure product quality and integrity.

After completion of manufacturing of every batch, the Quality Assurance Department thoroughly reviews the batch documents, including the test reports, and releases the product for distribution. Samples are retained from every batch for monitoring, and real time stability study is conducted.