Blog - Medical Devices

Building Trust : Medical Device Testing in ISO 17025 Certified Laboratory

Building Trust : Medical Device Testing in ISO 17025 Certified Laboratory ISO 17025 is an international standard that sets out the requirements for the competence of testing and calibration laboratories. Laboratories that comply with this standard demonstrate their ability to

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Beyond the Blueprint: How Biocompatibility Testing Safeguards Patients Every Step of the Way

Beyond the Blueprint: How Biocompatibility Testing Safeguards Patients Every Step of the Way Medical devices play a crucial role in modern healthcare, but ensuring their safety and efficacy is paramount. Biocompatibility testing is an essential step in this process, evaluating

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Making in India, Healing India: The Future of Domestic Medical Device Manufacturing

Making in India, Healing India: The Future of Domestic Medical Device Manufacturing The medical device industry in India is experiencing a period of significant growth and change. The market is expected to reach a value of $25-30 billion by 2025,

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How To Register Medical Devices in India?

How To Register Medical Devices in India? Central Drug Standard Control Organization (CDSCO) has released the Medical Devices amendment rule and classification of non-notified medical device and In-vitro diagnostics (IVD’s) and according to that devices have been classified into 24 categories

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