Tel: 0129-4001010 Phone: +91 730 321 5033
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 Dialysis Machine is a medical device that plays a crucial role in filtering excess waste and fluid from the blood. It operates by mixing and monitoring the dialysate a fluid used to remove unwanted products from the blood while maintaining proper electrolyte and mineral levels. Additionally, the machine regulates blood pressure and flow, ensuring effective treatment for patients with kidney failure.
CDSCO Medical Device Registration is a regulatory process required to obtain approval from CDSCO to ensure the efficiency, safety, and quality of medical devices. This registration process involves evaluating each application based on device type, applicant details, operational scope, and home country approval. CDSCO grants licenses for device testing, import, or manufacturing after thorough evaluation.
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 Dialysis Machines include:
Safety & Quality Assurance: CDSCO registration ensures that dialysis machines meet high safety and quality standards, protecting public health by confirming that devices are free from harmful components.
Public Health Protection: CDSCO aims to bring transparency and accountability to its services, ensuring that all medical devices, including dialysis machines, are safe, effective, and of high quality.
Market Access:CDSCO registration is essential for entering the Indian market. It ensures that medical devices comply with regulatory standards, unlocking new opportunities for manufacturers and importers.
The following documents are required for CDSCO registration of Dialysis Machines.
Form 40
ISO 13485 Certificate
Full Quality Assurance Certificate
CE Design Certificate
Undertaking that all details provided are authentic
Free Sale Certificate or Certificate from the Foreign Government
Plant Master Report
Device Master File
Obtaining CDSCO Registration for a dialysis machine is a crucial step, especially given the Indian Government's move to include all medical devices, including implants and contraceptives, under CDSCO scrutiny. Apply for your registration certificate or import license through the Licensing Authority at CDSCO to ensure compliance and market access.
CDSCO stands for Central Drugs Standard Control Organisation**. It is India’s primary regulatory authority responsible for overseeing cosmetics, pharmaceuticals, and medical devices.
CDSCO registration for a dialysis machine is the process of obtaining approval from the Central Drugs Standard Control Organisation to ensure the device's efficiency, safety, and quality. The primary goal of this registration is to safeguard public health by verifying that the device meets stringent regulatory standards.
To initiate the CDSCO medical device registration process, sign up on the SUGAM portal available on the official CDSCO website. This portal facilitates the submission and tracking of your registration application.
Applicant's details and address proof, a description of the medical device, legal documentation, post-market surveillance (PMS) report, plant master file, device master file, and other relevant regulatory certificates.