IcglobalblogusI3CGLOBAL US INC — Medical device consultants in the USAMedical device consultants in the USA provide a range of services to medical device manufacturers, including regulatory compliance support…Mar 25, 2023Mar 25, 2023
IcglobalblogusEUDAMED Actor RegistrationEUDAMED actor Registration, SRN activation and UDI is the IT system made of 6 interconnected modulesMar 25, 2023Mar 25, 2023
IcglobalblogusMHRA RegistrationMHRA Registration is mandatory for sale of medical devices in UK after the Brexit. Foreign manufactures contact us for support!Feb 27, 2023Feb 27, 2023
IcglobalblogusWhy You Need Medical Devices CE Marking And How to Get It:A blog that describes medical device directives and requirements.Feb 27, 2023Feb 27, 2023
IcglobalblogusUnderstanding Medical Devices Regulations to Guarantee ComplianceThe Food and Drug Administration (FDA) facilitate each and every clinical device that is advertised and utilized by the clinical industry…Jan 25, 2023Jan 25, 2023
IcglobalblogusUKCA REGULATION & Certification Process — i3CGLOBAL.USBefore jumping to the process directly, first let us know what is UKCA Marking,Jan 25, 2023Jan 25, 2023
IcglobalblogusFDA Software As a Medical DeviceFDA Software As a Medical Device (SaMD) is essential for marketing in U.S. The below page details few information about the approval…Jan 25, 2023Jan 25, 2023
IcglobalblogusThe CE marking, the guarantee of your medical productsThe CE marking is the seal of quality and safety that all products sold within the European Union must have, regardless of whether they are…Dec 28, 2022Dec 28, 2022
Icglobalblogus510k ConsultantsFDA 510k Consultants help you navigate the complete process for Class I, Class II, and Class III devices by thoroughly understanding the…Dec 28, 2022Dec 28, 2022
