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Guide to Choosing Medical Device Distributor and Regulatory Consultants in India
Entering the Indian medical device market is a strategic decision
Make in India Public Procurement Order 2017 Boosts Industry
On July 19, 2024, the Department for Promotion of Industry
Legal Meteorology Requirements, Medical Devices, India
Legal Metrology Compliance Are you a manufacturer or importer of
Testing and Evaluation for Medical Devices/ IVD’s , India
On May 29, 2024, the Central Drugs Standard Control Organisation
India Drug Barcode New Regulations: Enhancing Safety and Compliance
In a significant move to enhance drug safety and combat
E-Waste Management for Medical Devices in India
E-Waste Management for Medical Devices in India is crucial for
Medical Device Labeling Requirements in India
Labeling for medical devices in India is very important for
Medical Device Re-Registration/Renewal Process, CDSCO, India
Manufacturers should follow the guidelines issued by the Central Drugs
CDSCO Drug Safety Compliance: Ensuring Pharmaceutical Quality in India
The Central Drugs Standard Control Organisation (CDSCO), under the Directorate
SEC – Special Expert Committee, Medical Devices
SEC – Special Expert Committee, India Update: In the process
High-Value Medical Equipment: Customs Exemptions
High-Value Medical Equipment: Customs Exemptions In June last year, the
MD-15 Import License, India
MD-15 Import License: In the constantly evolving regulatory landscape of
Cosmetic Import Compliance in India: CDSCO’s New Directive
Cosmetic Import Compliance: Under the 2020 Cosmetics Rules, for importing
India Drug Pricing Reforms: New Framework and its Impact
Currently, the NPPA follows the regulations which are outlined in
PSUR India, CDSCO’s Online Submission Requirement
PSUR – Periodic Safety Update Reports The Central Drugs Standard