Global Regulatory Harmonization Efforts in 2025
Global regulatory harmonization efforts in 2025 focus on aligning different countries’ laws and standards to create a more unified system for international
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Global regulatory harmonization efforts in 2025 focus on aligning different countries’ laws and standards to create a more unified system for international
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Cybersecurity and data privacy in connected and wearable devices like smartwatches, fitness trackers, glucose monitors, and medical wearables have become very popular.
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The use of AI and Machine Learning in Medical Devices is transforming healthcare by enabling faster diagnosis, personalized treatments, and predictive care.
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How to Apply for a Manufacturing License for Patient Monitors in India is a very important process for any company planning to
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CDSCO Anaesthesia Medical Devices Registration in India is a mandatory requirement for manufacturers and importers who wish to market anaesthesia-related devices in
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Custom clearance issues for medical devices are one of the most common challenges faced by importers in India. Since medical devices directly
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A European Authorized Representative for Medical Device Companies is essential for non-EU manufacturers who want to sell their products in Europe. Under
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The Medical Device Regulations, 2017 (MDR 2017) were introduced by the Ministry of Health and Family Welfare to create a structured legal
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MedTech Mitra Incubation is a government-backed initiative launched in India to support innovators, startups, and researchers in developing affordable and high-quality medical
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Medical Device Parks in India are special industrial hubs developed by the government to boost local manufacturing of medical devices. These parks
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