Year: 2026

CDSCO Registration for Medical Devices

CDSCO Registration for Medical Devices

Any manufacturer, importer, or marketer planning to sell medical devices in India must comply with CDSCO registration and licensing requirements as per the Medical Devices Rules (MDR), 2017. What is CDSCO Registration for Medical Devices? CDSCO registration is a mandatory regulatory approval required for medical devices notified under MDR 2017.…
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BIS Certification for HDPE Woven Sacks

BIS Certification for HDPE Woven Sacks

As per the latest notification issued by the Ministry of Chemicals and Fertilizers, HDPE (High Density Polyethylene) woven sacks have been brought under mandatory BIS certification through amendments to the Quality Control Orders (QCOs). This quality control is to ensure the product quality, safety and standardization. BIS Quality Control Order…
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Certification