Indian MDR – Deadline Approaching for Non-Notified Medical Devices
Introduction: Indian MDR – Deadline Approaching for Non-Notified Medical Devices This article deals with the Indian MDR Deadline Approaching for Non-Notified Medical Device Registration. The Central Drugs Standard Control Organization (CDSCO) is the Indian Advisory Body for Pharmaceuticals and Medical […]
Read MoreAmendments 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 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 MorePrice Cap on Stents in India
Introduction to Cardiology Market in India – Price Cap on Stents in India Price Cap on Stents in India plays a major role for Manufacturers who are looking to import into India. The Indian Cardiology market is expected to Grow […]
Read MoreRegistration and Importation of Cosmetic Products in India
Introduction – Registration and Importation of Cosmetic Products in India Registration and Importation of Cosmetic Products in India is governed by the Drugs & Cosmetics Act, 1940. The Cosmetic Industry is a booming Industry in India with a huge market for […]
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