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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.
General Hospital Medical Devices encompass a broad range of equipment and supplies used by healthcare professionals to support patient care and ensure safety. These devices are designed for various medical and surgical purposes and fall under the same category. Examples of General Hospital Medical Devices include Hydraulic Adjustable Hospital Beds, Therapeutic Medical Blinders, Neonatal Eye Pads, and Jet Lavage systems.
CDSCO registration is a crucial process for obtaining official approval from the Central Drugs Standard Control Organisation (CDSCO), India’s regulatory authority. This registration ensures that medical devices meet the required standards of efficiency and quality. The process varies based on the type of device, applicant details, operational aspects, and previous approvals from other countries. CDSCO evaluates each application meticulously before granting licenses for device testing, importation, or manufacturing.
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.
Obtaining CDSCO registration for General Hospital Medical Devices offers several key benefits: :
Access to the Indian Market: India, with its vast pharmaceutical and medical device market, allows manufacturers and importers to reach a broad consumer base upon CDSCO registration.
Enhanced Safety Assurance: CDSCO’s primary goal is to protect public health. The registration process involves rigorous quality checks to ensure the safety and efficiency of medical devices.
Increased Brand Credibility: Achieving CDSCO registration boosts a manufacturer’s brand recognition and credibility by demonstrating compliance with high safety, efficacy, and quality standards.
The following documents are essential for the CDSCO registration process for a General Hospital Medical Devices:
Application Form MD 40
Power of Attorney
Certificate of quality assurance
Challan TR6
Plant-Master File
ISO 13485 certificate
An Undertaking declaring that the information stated is correct
Device-master file
Free sale certificate
The Central Drugs Standard Control Organisation (CDSCO) serves as India's primary regulatory authority for issuing licenses for specialized medical devices. Securing a CDSCO license not only enhances your brand’s reputation but also provides several significant advantages, ensuring your products meet stringent quality and safety standards.
For a comprehensive guide and assistance with documentation for registering pain management medical devices, contact Absolute Veritas.
CDSCO stands for the Central Drugs Standard Control Organisation, India's key regulatory body for drugs and medical devices.
The CDSCO registration portal is called Sugam.
CDSCO Registration is a regulatory approval process designed to ensure the quality and efficiency of pharmaceuticals, medical devices, and cosmetics.