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Join the elite institute shaping the future of Medtech quality and communication.
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Workshop in Indian MDR 2017
ISO 13485: 2016 Lead Auditor Training
Awareness of Risk Management
1 day workshop on Pharmacovigilance & Materiovigilance- The Future of Integrated Safety Monitoring
EU MDR
Purple building certification Scheme
US FDA
ISO 14971 : 2019 - Risk management requirements for Medical Devices
Hands-on Training Program on Hemovigilance Practices
Training program on Biomedical Equipment Maintenance Certification Scheme
Training on ISO/IEC 17025:2017
ISO 13485: Internal Auditor Training
Certificate in Quality Assurance
Advanced Training Program in Biovigilance and Safety Monitoring
Training program on HEALTEXPROF
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