India Drug Barcode New Regulations: Enhancing Safety and Compliance
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In a significant move to enhance drug safety and combat counterfeit medicines, the Ministry of Health and Family Welfare, Government of India, has amended Rule 96 of the Drugs Rules, 1945. The amendment, detailed in G.S.R. 823(E) dated November 17, 2022, mandates the inclusion of Bar Codes or Quick Response (QR) Codes on the packaging of specified drug formulations. This regulation, enforced by the Central Drugs Standard Control Organization (CDSCO), aims to improve the traceability and authentication of drugs, ensuring that consumers receive genuine and safe pharmaceutical products. The new requirements came into force on August 1, 2023. These changes are part of the broader India drug barcode regulations designed to ensure drug integrity and public health safety.
Key Labeling Requirements as Per the Amendment
Mandate for Barcodes or QR Codes:
Additional Information
Unique Product Identification Code:
Scope of Applicability:
Applicability to Domestic and Foreign Manufacturers:
Batch-Specific Requirements:
Handling Inadequate Space on Labels:
Provisions for Imported Products:
Conclusion
The amendment to Rule 96 of the Drugs Rules, 1945, mandating Barcodes or QR Codes on drug formulations, marks a significant step towards enhancing drug safety and traceability in India. By ensuring that detailed and accurate information is easily accessible, this regulation helps protect consumers from counterfeit drugs and supports the overall integrity of the pharmaceutical supply chain. For manufacturers and importers, understanding and? implementing these new requirements is crucial. Partnering with regulatory companies like Morulaa can provide the necessary guidance and support to navigate these changes effectively, ensuring compliance with the Medical Device 14 (MD-14) standards and maintaining market readiness through the SUGAM portal for drug registration. CDSCO plays a critical role in this regulatory framework.
Morulaa: Your Regulatory Partner
Morulaa is well-versed in CDSCO regulations and can assist with the registration and compliance of medical devices in India. Whether it's navigating the complexities of the SUGAM portal or ensuring adherence to MD-14 standards, Morulaa offers comprehensive regulatory services. With a focus on India, Morulaa understands the local market dynamics and regulatory landscape, making it an ideal partner for medical device registration and compliance. To know more about how we can support you, Click Here or email us at [email protected].