The US Food and Drug Administration (FDA) is responsible to ensure that the public health and safety ae not compromised through the products that are intended for human and animal consumption. Hence, FDA laid regulations for maintaining the safety of instruments in calibration services.  The FDA has a code of regulations for medical device calibration requirements, which are stated in part 820 of its Quality System Regulation (QSR), Section 72. Title 21 of Code of Federal Regulations (CFR) part 820.72. This deals with inspection, measuring, and test equipment.  The regulation requirements of FDA for medical device calibration are not for specific measures. The regulations have been designed to ensure that the inspection, measuring, and the test equipment satisfy the intended use and quality requirements. The regulations act as guidelines for the manufacturers and distributors of medical equipment and devices, as they define the procedures, accuracy standards, and frequency of calibration that must be followed for calibrated equipment.

1. INTRODUCTION

2. RESEARCH METHODOLOGY 

3. EXECUTIVE SUMMARY

4. MARKET DYNAMICS

5. MARKET SEGMENTATION

6. COMPANY PROFILES AND COMPETITIVE LANDSCAPE

7. MARKET OPPORTUNITIES AND FUTURE TRENDS