Naprod’s core purpose and commitment is to consistently deliver safe and effective products to patients; a mission that everyone in Naprod believes passionately.
We at Naprod, maintain a quality-focused approach to ensure that top priority is placed on the safety, efficacy and reliability of our products. The safety of our patients and consumers, the quality of data supporting regulatory submissions and communication with our business partners/stakeholders.
Naprod leadership has appropriate systems and processes in place to ensure the consistency of quality of drug products.
Every single employee is committed to maintaining a quality culture with high compliance and processes to ensure product quality and patient safety meeting the established requirement of our customers/regulatory requirements and business.
We effectively involve all our employees and vendors in our endeavour to exceed customer expectations, to prevent defects and continually improve our processes to add value to the businesses we work with.
In line with our philosophy of knowledge-led growth, we have invested in a state-of-the-art F & D facility. Our research team has highly qualified scientists with doctoral experience from leading universities/institutions and is engaged in drug delivery systems, process development, analytical research and has cross functional lead.
Formulation development is a key area of product development that can determine patentability, life cycle and ultimately, the success of a pharmaceutical product. Formulation Development integrates functions and personnel into their product development cycle in many different ways, from early development lab scale to scale up to production scale technology transfer at site and off-site.
Formulation Development is a completely dedicated department for the development of a pharmaceutical product for the worldwide markets considering the patent and development strategy. Formulation Development also includes but is not limited to development of a stable and Bio-Equivalent Formulation and Transfer of the developed technology to the manufacturing site including dossier compilation and regulatory submission and addressing to any query from the regulatory agency to get the dossier approved in the coordination of cross-functional team (CFT).
Our R&D primarily focuses on
We have achieved significant success in the following thrust areas:
Our pharmaceutical products research team offer a portfolio of differentiated drugs and we have the ability to handle multiple dosage forms such as:
Our injectable portfolio includes Oncology injectables, Anesthetics, Steroids, and on development level Emulsions, Micro-emulsion, Suspensions.
With a portfolio of more than 500 products for various markets, the development team has vertically integrated operations for greater control: patent navigation, process development, scaling-up, tech-transfer, manufacturing finished formulations, registrations and supply chain management.
Naprod’s development arm has dedicated teams of highly qualified scientists working on development and registration of generic as well as branded products.