Skip to content
  • Home
  • About us
  • Events
  • Contact Us
  • Home
  • About us
  • Events
  • Contact Us

  • PROFESSIONAL COMPETENCE DEVELOPMENT

    MediTech Egypt
    intended to elevate
    Medical Device stakeholder's competence.

    Egypt Meditech is the platform for medical
    device interested parties in Egypt.

    Book Now

  • Regulatory Compliance & Technical Services

    Your Trusted Gateway to Global Medical Device Compliance

    Accelerate your market access with comprehensive technical support. We streamline your compliance pathways for Clinical Evaluation, Biocompatibility, and European MDR alignment.

    Book Now

  • Training, Workshops & Capacity Building

    Empowering Professionals with Advanced Regulatory Expertise

    Advance your career and scale your business capabilities. Participate in interactive, expert-led workshops specialized in Risk Assessment, Usability Engineering, and quality management.

    Book Now

    Welcome to Egmeditech

    Egypt MediTech is a place where all medical device and invitro diagnostic Regulators, manufacturers, and experts meet to shape the future of Medical device in Egypt.

    Join our 3rd Medical Device Conference June 2026

    What We 'll Cover

    Regulatory Alignment Overview

    MDR Annex I

    General Safety & Performance Requirements

  • Biocompatibility and biological safety.
  • Usability engineering and use‑related risk control.
  • Biocontamination and contamination prevention.
    • MDR Annex II

    Technical Documentation

  • Technical file structure and completeness.
  • Clinical evaluation, biocompatibility, usability, and testing documentation.
  • Evidence traceability and consistency.
    • MDR Annex III

    Post‑Market Surveillance

  • PMCF planning, execution, and reporting.
  • Feedback into risk management and clinical evaluation.
    • MDR Annex XIV

    Clinical Evaluation & PMCF

  • Clinical evidence lifecycle management.
  • PMCF as an ongoing regulatory obligation.
    • IEC 62366‑1

    Usability Engineering

  • Use‑related hazard identification.
  • Usability validation and documentation.
  • Support of MDR Annex I compliance.
    • General Safety & Performance Requirements
    Technical Documentation
    Post‑Market Surveillance
    Clinical Evaluation & PMCF
    Usability Engineering

    Moments From First Edition

    After the success of the first edition of the Medical Devices Conference, stay tuned for the second conference with medical device pioneers.

    01
    02
    07
    03
    04
    08
    05
    06
    09
    10
    11
    12
    13
    14
    15
    16
    17
    18
    19

    Interviews from 1st Round EG meditech Medical device conference

    Certificate Verification

    • Home
    • About us
    • Events
    • Contact Us
    • Home
    • About us
    • Events
    • Contact Us
    Facebook Linkedin

    Copyright © 2025 Egmeditech | Powered by Qualitech international

    Scroll to Top