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Email: cs@absoluteveritas.com
CDSCO stands for the Central Drugs Standard Control Organisation, India's national regulatory authority for cosmetics, pharmaceuticals, and medical devices.
The government has recently announced plans to bring all medical devices, including implants and contraceptives, under the review of CDSCO regulations.
A Blood Pressure monitor, also known as a Digital BP Monitor, is an essential digital medical device used to measure and track blood pressure readings in individuals. It is a critical diagnostic tool for monitoring blood pressure levels and ensuring accurate health assessments.
CDSCO Medical Device Registration is a vital process for obtaining approval from the Central Drugs Standard Control Organisation (CDSCO). This approval ensures the efficiency and quality of pharmaceuticals, medical devices, and cosmetics. The application process varies based on device type, applicant characteristics, operations, and home country approval. CDSCO issues licenses for device testing, import, or manufacturing after a comprehensive evaluation of each application.
Online Registration: Visit the official CDSCO website and access the 'SUGAM CDSCO Portal.' Click on the 'SIGN UP HERE' option to start your application.
Fill Out the Details:The registration form is divided into two sections: 'Applicant Details,' where you provide your personal information, and 'Registered Indian Address,' where you input your organization's details.
Document Submission: Complete the application by submitting all required documents for verification.
Verification of Registration :A confirmation link will be emailed to your registered address. Click on the link to activate your account on the SUGAM portal.
Approval from Authority: Once you confirm your registration, your application will be forwarded to the relevant authority for approval. If approved by CDSCO officials, you will receive an approval email. If rejected, you will be notified accordingly.
The benefits of obtaining CDSCO registration for BP Monitor include:
Indian Market Access: India has one of the largest markets for pharmaceuticals and medical devices globally. CDSCO registration allows manufacturers and importers to sell their BP monitors to Indian consumers.
Ensuring Safety: CDSCO's primary goal is to safeguard public health. The quality and efficacy of BP monitors undergo a rigorous verification process by CDSCO officials, ensuring safety and reducing health risks.
Brand Recognition:CDSCO registration enhances a manufacturer’s brand recognition and credibility by demonstrating compliance with stringent safety, efficacy, and quality standards.
The following documents are essential for the CDSCO registration process for a BP monitor:
Application Form MD 40
ISO 13485 Certificate
TR6 Challan
Power of attorney
Undertaking that all details provided are authentic
Full quality assurance certificate
Declaration of conformity
Device Master File
Plant master report
Free sale certificate
Under the Drugs and Cosmetics Act and Rules, 1940 and 1945, CDSCO is the national regulatory authority in India responsible for approving licenses for drugs, cosmetics, and medical devices. The CDSCO Medical Device Registration process for BP monitors is lengthy and complex, but you can rely on Absolute Veritas for complete guidance and support.
The Drugs and Cosmetics Rules, 1945, categorize drugs into specific schedules and outline guidelines for their storage, sale, display, and prescription. These rules are essential for maintaining the quality and safety of pharmaceuticals and medical devices in India.
Medical devices require CDSCO registration because the Indian Government mandates it to ensure the safety, quality, and efficacy of all medical devices, including implants and contraceptives. This regulation helps safeguard public health by ensuring that all medical devices meet strict standards.
Medical devices are categorized into four classes (A, B, C, D) based on their risk level. Class A represents the lowest risk, while Class D represents the highest risk. This classification helps in the proper regulation and management of medical devices according to their potential impact on health.