Our Services
Medical Inspection
Regulatory Requirements for Medical Equipment
Medical Product Testing Solutions
Environmental and Regulatory Services
Medical Management Systems Certification and Auditing
Scientific Support Services
Clinical Research Services
Pharmaceutical Services
Regulatory Requirements for Medical Equipment
 Medical devices are becoming more important in the health care sector. One of the major issues for companies developing and producing medical devices is to be updated on the regulatory requirements and implement them in the process.
Manufacturers of medical devices need to adjust to the regulatory framework in the country where the product is sold. This constitutes a great problem for manufacturers, especially for companies selling their products in several countries. Competent authorities worldwide have begun to realize the problem and collaborate to harmonize the regulations.

To bring your medical device to global markets with speed and efficiency, you need a testing and certification partner who knows your business. Count on G.I.T.O for auditing, Notified Body approvals, and compliance testing and certification to global standards and requirements, all from a single source.

Our global market entry program is your key to accessing the world’s fastest growing medical device markets. Learn how you can obtain multiple national safety certifications for your product and gain entry into more countries.