The company was incorporated in the year 2012 by an experienced technocrat, having more than two decades of experience in the pharmaceutical sector. Prowill Pharmaceuticals Pvt Ltd was established with an objective to provide a complete solution to the pharmaceutical industry and establish itself as a One Stop Shop. Due to the experienced team in respective areas, one man's initiative is now growing across multiple locations and beyond borders. Excellent GMP-certified infrastructure and Good Manufacturing Practices are the key factors behind the success of Prowill Pharmaceuticals Pvt Ltd. These strengths have enabled the company to achieve success in a short period of time and gain recognition from regulatory agencies. The mission of Prowill Pharmaceuticals Pvt Ltd is to become the most valuable partner for the world pharmaceutical fraternity. At Prowill Pharmaceuticals Pvt Ltd, we believe in brand building. Through continuous quality improvement, we ensure that our standards and reputation are consistently maintained. Our goal is to provide the highest quality generic drugs and the best possible service to our customers. At Prowill Pharmaceuticals Pvt Ltd, we proudly understand the complete pharmaceutical process, starting from raw material synthesis and formulation to efficacy testing and product registration.

With expertise across a wide range of formulations, including tablets, capsules, liquids, ointments and novel drug delivery systems, Prowill Pharmaceuticals Pvt Ltd is recognized as one of the fastest-growing pharmaceutical companies.

Facility I – Antibiotic Facility

Prowill Pharmaceuticals Pvt Ltd has a dedicated manufacturing facility for a wide range of antibiotic products, including tablets, capsules and dry syrups.

Facility II – Oral Solid Dosage Formulation

Prowill Pharmaceuticals Pvt Ltd manufactures products other than antibiotics from a dedicated manufacturing site equipped with facilities for tablets, capsules and dry syrups.

Facility III – Liquid & Ointment

Prowill Pharmaceuticals Pvt Ltd manufactures a large range of liquids, syrups and ointments to meet diverse pharmaceutical requirements.

The Quality Control and Analytical Research & Development Department supports all developmental activities and provides comprehensive support for Active Pharmaceutical Ingredients and formulation development. The department is well equipped with highly sophisticated instruments and advanced laboratory facilities, including:

• LCMS
• High Performance Liquid Chromatography (HPLC)
• Gas Chromatography (GC)
• UV Spectrophotometers
• Infra-Red Spectrophotometer
• Dissolution Apparatus
• Microbiology Laboratory
• Stability Chambers

Prowill Pharmaceuticals Pvt Ltd has a significant presence in international markets, which constitute around 80% of its annual sales income. From the early days, the company recognized that timely product registration with the health authorities of respective countries would be a key factor in successfully entering and expanding within international markets. Over the years, we have gained an in-depth understanding of the regulatory frameworks of various countries and have developed strong regulatory filing capabilities with competent manpower to accelerate product registration dossiers. Our Drug Regulatory Affairs (DRA) team is involved in product registrations across various domestic, emerging and regulated markets across different continents. The core responsibility of our DRA team is to register products in international and domestic markets and enable market entry within the shortest possible time. The team comprises highly qualified pharmacists who focus on understanding the prerequisites and latest developments in Food and Drug Administration (FDA) guidelines and product registration requirements across the globe. Continuous training is provided to the team to ensure that they remain up to date with constant changes and developments in the requirements of various regulatory authorities.