Class II Medical Devices: Meaning, Requirements, Process
Running the healthcare system without the use of medical devices is nearly impossible. Medical devices have become an integral part […]
Class I Medical Device: Regulatory Classification
In the US, Center For Devices And Radiological Health (CDRH) which is a branch of FDA is the regulatory body
Medical Devices Regulation With PFDA In Philippines
In the Philippines, the medical device industry relies heavily on imports for its products. Whether these products are made
Medical Devices Regulations in Hong Kong
Hong Kong’s vibrant medical and healthcare equipment and devices sector primarily focuses on catering to the needs of the household
Hong Kong: New Drugs, Generics, Biosimilars Regulations
Hong Kong- New Drugs, Generics, Biosimilar Regulations: Hong Kong has a robust regulatory system for pharmaceuticals, overseen by the Department
Medical Device Registration in USA by US FDA
The responsibility for overseeing the regulations of medical device companies involved in the production, repackaging, relabeling, and medical device registration
510(k) Registration with US FDA – Medical Device Registration in USA
Medical devices regulatory compliance is paramount to ensure patient safety and effective product performance. The 510(k) registration process, overseen by
Digital (SEO) Strategies for a USA based Surgical Instruments Company
Summary Boosting Surgical Company’s digital presence, driving improved website performance, and fortifying their reputation in the competitive medical equipment industry.
Biologics and Biosimilars Regulations, Registration Process in the USA (FDA)
The size of the U.S. biosimilars market, estimated at USD 6.73 billion in 2021, is expected to increase by USD