Parenteral Drugs (India) Ltd has its manufacturing unit located at Kasrawad, Madhya Pradesh, was set up in 2015. Parenteral Drugs (India) Ltd, Baddi was set up in 2006.These facilities are at par with global standards highlighting PDIL's dedication towards quality and safety.
We have established State-of-Art FFS technology & Glass bottle LVP products with a motto to provide quality products to the consumers. PDIL believes that quality has to exist inherently and thus it is the people who make that difference as each & every person working tries to add value in their functional area.
As per Schedule M for manufacturing of Large volume parenterals in plastic containers, it is advisable to install automatic (with all operations) Form-Fill-Seal machines having one continuous operation. The world class machines are having patents granted in United States and Europe for its superior technology.
We at PDIL believes that implementation of an effective quality assurance policy is the most important goal of organization. The concept of quality assurance and quality control together develops towards assuring the quality, safety and efficacy of pharmaceutical products. Thus quality is critically important ingredient to organizational success. Which can be achieved by the total quality management (TQM), an organizational approach that focus on quality aimed at the prevention of defects rather than detection of effects.Quality Control
Being among the most technologically advanced with wide range of large volume parenterals (LVPs) we ensure the highest quality standard during manufacturing and extreme care is taken in every stage of operation in order to maintain stringent class conditions.
Quality Control Laboratory as per cGLP standards, set up for the purpose of efficient functioning.
Quality system standards are continuously upgraded by the firm by issuing Quality System Guideline from time to time which becomes the basis for formulating standard operating procedures. The Corporate Quality System also carries out internal audits of all manufacturing plants to check compliance with current Good Manufacturing Practices (cGMP).Quality assurance
Well established quality assurance systems and procedures provided. Two factors are of outright importance here: quality and safety. We place the strictest demands on the reliability of our products and services. Quality assurance is therefore a firm component of our activities in all areas.