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Biomedical Industrial Training Program

NTHRYS >> Services >> Industrial Services >> Training Programs >> Biomedical Industrial Training Program

Biomedical Industrial Training Program

This program is designed for biomedical students and job seekers who wish to gain industry-relevant exposure in product testing, production QC, standardization of biomedical devices, and regulatory audits as per ISO/NABL norms.
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Info @ +91-8977624748
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Note: Below modules are designed keeping high end industrial professionals into consideration. Please refer individual protocols below for affordable prices.
Industrial QA/QC and Product Standardization
Biomedical Training Module
    Fee: Contact Us

    Protocols List

  1. QC checks for diagnostic reagents and assay kits
  2. Performance validation of diagnostic devices
  3. Batch testing and lot release documentation
  4. Root cause analysis and CAPA for non-conformities
Regulatory Documentation and Compliance
Biomedical Training Module
    Fee: Contact Us

    Protocols List

  1. Preparing SOPs for production and QC workflows
  2. Internal audits and proficiency testing participation
  3. Documentation for FDA or CDSCO registration
  4. Case studies on regulatory non-compliance and recall handling
Industry Exposure and Reporting
Biomedical Training Module
    Fee: Contact Us

    Protocols List

  1. Sample traceability and barcoding in production lines
  2. Calibration logs for biomedical devices
  3. Material safety data sheets (MSDS) usage
  4. Final project: validating a diagnostic kit and reporting results

Individual Protocols Under Biomedical Industrial Training Program

  1. QA principles in biomedical product manufacturing | Fee: Contact Us
  2. QC checks for diagnostic reagents and assay kits | Fee: Contact Us
  3. Performance validation of diagnostic devices | Fee: Contact Us
  4. Batch testing and lot release documentation | Fee: Contact Us
  5. Root cause analysis and CAPA for non-conformities | Fee: Contact Us
  6. ISO 13485 and NABL standards for biomedical companies | Fee: Contact Us
  7. Preparing SOPs for production and QC workflows | Fee: Contact Us
  8. Internal audits and proficiency testing participation | Fee: Contact Us
  9. Documentation for FDA or CDSCO registration | Fee: Contact Us
  10. Case studies on regulatory non-compliance and recall handling | Fee: Contact Us
  11. Mock industrial QC audits and reporting practice | Fee: Contact Us
  12. Sample traceability and barcoding in production lines | Fee: Contact Us
  13. Calibration logs for biomedical devices | Fee: Contact Us
  14. Material safety data sheets (MSDS) usage | Fee: Contact Us
  15. Final project: validating a diagnostic kit and reporting results | Fee: Contact Us

Please contact on +91-8977624748 for more details

Cant Come to Hyderabad or Chennai or Bangalore? No Problem, You can do it in Virtual / Online Mode




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