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Savi Rapid Diagnostics Company

Savi Rapid Diagnostics Company is founded by Mr. Jatinder S Sabharwal (CEO) in year 2007 with an objective to manufacture Blood bags, Diagnostics, Pharmaceutical formulations and Medical Devices.

The company is supported by several functions like Finance, Projects, Technical Services, Research and Development, Marketing, Human Resources Management, Information Technology, and Audit which are corporate in nature.

Our Company

SAVI RAPID DIAGNOSTICS COMPANY is a professional manufacturer and distributor located at Ahmedabad-Gujarat and Palghar-Maharastra. SRDC has developed a range of diagnostics products, Blood Bags, laboratory consumables , pharmaceutical formulations at our manufacturing facility. Our Aim is to provide High quality products and services to our Customers at all times.

Our Diagnostics Products Include:

Rapid test, clinical Chemistry, laboratory consumables and Instrumentation for laboratory setup We are an FDCA, ISO 13485 2016 certified diagnostics products manufacturer. We are also Keen to take orders and work as Agent for other diagnostic companies. Supported by our professional personnel and good Manufacturing Practice, we will always offer the Best Quality to our esteemed Customers.

Quality Policy

We shall be committed to manufacture products following rigidly our quality management system which shall comply and compete with most stringent international standards and hence strive towards zero defect performance of all our products.

We shall be always driven by quality with technology which is aimed at competing with our own standards to achieve still higher levels of qualitative performance in all aspects of our work.

SRDC has developed a quality management system which ensures to establish and maintain a documented quality system as a method of assurance that our products conform to the specified requirements, which are in accordance with the CGMP/Revised schedule-M requirements.

Our System includes the preparation and effective implementation of documented quality assurance procedures, the details of the management system is mentioned in the respective departments Standard Operating Procedures (SOP) manual.

The SOP manual defines the quality related responsibilities which are required in the daily operation of the factory and also describes the written procedures which give in detail the activities and responsibilities of all personnel involved in operating and administering the quality system.

The periodic and formal review of the effectiveness of the firms quality systems, and their revision where necessary shall be the responsibility of the internal quality audit team, which comprises of members from all departments.

The Quality audit team reviews and monitors the effectiveness of the system by monitoring the following:
Incoming material, Product Quality, Compliance with system and Document control, Customer Complaints and feed back, Corrective Action, Internal Quality Audits.