Fire extinguishers system present throughout the plant
Vaasavaa
Pharmaceuticals (P)Ltd,
Analysis of raw materials, in-process, intermediates, and finished products as per the specifications and standard test procedures.
Quality System
Different departments involved in the production and distribution of the products are Quality Assurance , Quality Control, Production, Warehouse, Maintenance, Other departments (Human resources, Marketing and Purchase)
Vaasavaa Pharmaceuticals Private Limited develops and produces specified Drug Intermediates and Active Pharmaceutical Ingredients (APis)
Company Profile
Vaasavaa Pharmaceuticals (P) Limited develops and produces specified Active pharmaceutical Intermediates and Active Pharmaceutical Ingredients (APIs). It was incorporated as Private Limited company Under Companies Act, 1956 at Plot No. C-216 & 217, MIDC, Chincholi, Solapur-413 255, Maharashtra, INDIA, about 300 Km away from Hyderabad. The manufacturing site is located between Hyderabad and Pune, Maharashtra and it is well connected by road and railway. Nearest domestic airport is located at Solapur, and the nearest international airports are Hyderabad and Pune. The Corporate Head Quarters strategically situated at Flat No. 201, 3rd Floor, Plot No. 32-27, H. No. 2- 227, Deeksha Hospital Building, Sardar Patel Nagar, Kukatpally, Hyderabad-500072. The Administration, Marketing, Sales, Purchase, Finance & Accounts Divisions are housed in the Corporate Office. Vaasavaa Pharmaceuticals Private Limited is engaged in the manufacturing of Active pharmaceutical ingredient and its intermediate segments for catering to the domestic as well as international market. Vaasavaa has consistently delivered quality products with value added services. Vaasavaa is Uncompromising product quality underlines the core competence of the company. The facility is certified for WHO GMP and DCA GMP Certification.
Read moreOther Activities
Medical facility available
Scheduled medical check up carried out for all employees
Solid waste: TSDF, Ranjangaon
Liquid effluent: Greenfild CETP, MIDC Chincholi
Production Activities
- Planning to manufacturing the batches.
- Raw Material requisition to Warehouse.
- Placing materials with clear identification in the production blocks.
- Receiving BMRs from Quality Assurance.
- Execution of batches.
- Sampling and sending request for analysis to Quality Control
- Yield calculation.
- Upon completion of batch, handing over the Batch Manufacturing Records to Quality Assurance Department.
- Cleaning of Production areas.
- Packing of Dispatch material.
- Investigate the Batch failures coordinate with QA.
Quality Policy & Quality Objectives
QUALITY POLICY
We, at Vaasavaa Phannaceuticals Private Limited are committed to achieve excellence in quality standards by adhering to the regulatory and statutory guidelines and supply quality APis and Intermediates as per the customer requirements. We shall strive to become globally respected partner through technical capabilities and inducing high degree of customer satisfaction .
QUALITY OBJECTIVES
Monitor consistency of the Product Quality through Product Quality Reviews.
Strive for the up-gradation of the technology to meet customer requirements.
Complying with GMP requirements, and upgrading manufacturing facilities where required.
Providing appropriate training to all employees for effective implementation of the Quality Management System.