Quality policy
At Savi Health Science we follow high quality standard and fully comply with legislative requirements as well as cGMP guidelines so as to ensure quality of our medicines, quality of the service we provide and customer satisfaction . Since One decade our company has been applying a cirtified quality management system for the activities of ” Import, storage , Distribution , and sales of pharmaceuticals Products according to the cGMP standard.
Savi Health Science has in house facility of Microbiology, Chemical Laboratory and Instruments Labs , which are responsible for incoming raw material and packing inspection and testing and in process and release testing of bulk product and finished goods .All testing requirement are established to meet current regulations and current needs . Quality Control is also responsible for monitoring of our facility.
Quality Assurance
The Quality Assurance department is responsible for the confirmation that products produced at Savi Health Science meet all WHO-GMP and customer requirements. This and compliance with WHO-GMP drug product and medical device regulations are achieved by Quality Assurance oversight and interaction throughout the facility. This includes educating, and promoting cGMP compliance as well as risk based management. The Quality Assurance Department performs, offers, and supports a wide range of cGMP and regulatory services, including:
- Annual Product Reviews
- Complaint File handling and investigation
- Document Control
- Artwork and label review
- Quality internal and external auditing
- Preparation of Quality Agreements
- Regulatory filings and submissions
Microbiology
Our key objectives of pharmaceutical microbiology is to ensure safety and efficacy of Pharmaceuticals product . we embraces the processes like the validation of disinfectants, evaluation of the efficacy of disinfectants in suspension, on surfaces, and through field trials. Our team offers protocols and techniques associated with the operation and assurance of clean-room, aseptic-room and controlled environments for preventing any possible microbial contamination, and introduces risk assessment and practical contamination control strategies.Simply,
we manage all microorganisms, e.g., bacteria, fungus and viruses. We also maintain microorganisms like pharmaceutical contaminations, and degradation, deterioration and spoil of pharmaceutical raw materials and finished products.