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 […]
MedTech
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
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
MedTech, US FDA Compliance
Q-Submission Meetings for Medical Devices with US FDA
The US Food and Drug Administration (US FDA) Q-Submission Program serves as a vital channel for medical device manufacturers to
Medical Device Regulations and Registration In UK (MHRA)
Medical Device Regulations and Registration Process in the MHRA United Kingdom (UK) The publicly funded National Health Service (NHS) is
UKRP Responsibilities for Medical Device Manufacturers Outside the UK
For medical device manufacturers located outside the United Kingdom (UK) without local business offices, it is mandatory to designate a
FAQ – Singapore (HSA) Regulations for Medical Device Registration
Here are answers to some of the Frequently Asked Questions (FAQs) about Singapore regulations for Medical Device registration. FAQs –
HSA Medical Device Dealers Licenses in Singapore
The Health Sciences Authority (HSA) functions as the regulatory authority responsible for overseeing medical devices within the country, ensuring their