Amendments in Medical Devices Approval in the field of Anesthesiology
Background – Amendments in Medical Devices Approval in the field of Anaesthesiology This article deals with the Medical Devices Approval in the field of Anaesthesiology. The Central Drugs Standard Control Organization (CDSCO) is the Indian Advisory Body for Pharmaceuticals and Medical […]
Read MoreRegulatory Consultancy for Medical Device Amendments in Cardiovascular Devices
Background: Regulatory Consultancy for Medical Device Amendments in Cardiovascular Devices This article deals with the Regulatory Consultancy for Medical Device Amendments in Cardiovascular Devices. The Central Drugs Standard Control Organization (CDSCO) is the Indian Advisory Body for Pharmaceuticals and Medical […]
Read MoreIndian MDR Amendments in Dermatological and Plastic Surgery
Background – Amendments with the Indian MDR This article deals with the regulatory affairs for the Indian MDR. This amendment is for the Intended Use for Medical devices in Dermatological & Plastic Surgery. The Central Drugs Standard Control Organization (CDSCO) controls […]
Read MoreMedical Device Amendments for Devices Used in Physical Support
This article deals with the Amendments in the Intended Use of Medical Devices in the field of Physical Support. The Central Drugs Standard Control Organization (CDSCO) is the Indian Advisory Body for Pharmaceuticals and Medical Device Regulations in India wherein […]
Read MoreMedical Device Amendments in the Field of Rehabilitation
Background – Regulatory Affairs for Medical Devices This article deals with the Regulatory Affairs for Medical Devices. This amendment is for the Intended Use for Medical devices in Rehabilitation. The Central Drugs Standard Control Organization (CDSCO) controls the Regulatory Affairs for […]
Read MoreMedical Device Amendments – Interventional Radiology
Background This article deals with the Medical Device Amendments – Interventional Radiology. The Central Drugs Standard Control Organization (CDSCO) is the Indian Advisory Body for Pharmaceuticals and Medical Devices wherein all Notified Medical Products are regulated by them. The responsibility […]
Read MoreValidation of Rapid Antigen Test (RAT) for COVID-19 in India
This article deals with the Validation of Rapid Antigen Test (RAT) for COVID-19. The ICMR invites applications for the validation of the Rapid Antigen Tests (RAT) which is mainly used in the diagnosis and detection of SARS-CoV-2 in India. They […]
Read MorePC & PNDT Approval for Ultrasound Import into India:
Introduction – PC & PNDT Approval for Ultrasound Import into India This article deals with the PC & PNDT Approval for Ultrasound Import into India: for the import of Ultrasound into India. As per the Pre Conception and Pre Natal Diagnostic […]
Read MoreIntroduction to Medical Device Registration in Korea
Introduction to Medical Device Registration in Korea This article deals with the Medical Device Registration in Korea. South Korea ranks fourth among countries in the Asia-Pacific region’s healthcare market. The increase in the aging population, and the insurance coverage, along […]
Read MoreMedical Devices Registration in Philippines
Introduction – Medical Devices Registration in Philippines This article deals with the Medical Devices Registration in Philippines. The Philippines’ Food and Drug Administration (FDA), which functions under the Department of Health, issues the license, monitors, and regulates the flow of […]
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