Manufacturing Facility

IME Herbal Products Pvt. Ltd, has a quality control system for our manufacturing unit which makes us pioneers in providing better quality phyto-chemical and herbal extracts to our clients for their product requirements. Quality agreement and other processes which are a requirement for the smooth momentum of a manufacturing facility are maintained and International standards are complied with. The research and development unit in our facility is utilized to test product safety. Our suppliers of raw material also follow the Ethical code of conduct which has been laid down by the FDA thereby producing an effective cutting edge finished product. We specialize in state of the art technology manufacturing sectors such as natural plant extract products that are used for varied bio-pharmaceuticals, plasma-derived biological research, and cell culture media, filling capsules and working as a secondary active ingredient or a precursor for vaccines and other biologically-based diagnostics which require quality and purity. Manufacturing phyto chemical and herbal extract products in our facility involves many individual unit operations and activities, which are followed by our very dedicated staff. It is our promise to create a better living and healthier world by giving you the best products available. Procedures delineating the controls over sampling and testing samples have been established in the Quality Agreement to provide guidance to our technical team. The methods used to both test the product under process and to test the finished product are validated and have been transferred appropriately. Laboratory equipment used in the manufacturing facility and research sites follows CGMP certified equipment guidelines that are qualified, calibrated, and maintained in a controlled environment with the primary responsibility resting on the Quality control Analyst. The guidance that we follow describes our current thinking on defining, establishing, and documenting the responsibilities that we lay on our suppliers and the third parties involved in the manufacturing of drugs based on the Current Good Manufacturing Practice (CGMP). In particular, we lay guidelines in the product manufacturing and describe how parties that are involved in the facility of preparing of drugs can follow and utilize Quality Agreements to delineate the responsibilities and assure drug quality, safety, and efficacy to the clients.