Regulatory Compliance

Introduction to Software as a Medical Device Software as a medical device (SaMD) is rapidly transforming healthcare delivery in Algeria. With digital healthcare adoption increasing across hospitals, clinics, and diagnostic centers, SaMD solutions are now used for patient monitoring, diagnostics, AI-based imaging, and clinical decision-making. As the healthcare system evolves, Algeria’s regulatory authority continues to […]

Medical Device Validation Master Plan (VMP) in Algeria For medical device manufacturers in Algeria, compliance is the gateway to both local and international markets. Whether you want to sell in Algeria, the European Union (CE Marking), or the United States (FDA 510k / 21 CFR Part 820), one document you cannot ignore is the Validation