Career Advancement Programme in Medical Device Compliance

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Medical Device Compliance training is crucial for professionals seeking career advancement. This programme targets regulatory affairs specialists, quality engineers, and compliance professionals in the medical device industry.

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์ด ๊ณผ์ •์— ๋Œ€ํ•ด

Gain expertise in ISO 13485, FDA regulations, and EU MDR. Develop skills in risk management, auditing, and CAPA. Enhance your career prospects with this in-depth programme. Advance your knowledge and become a leader in medical device compliance. Register today and transform your career.

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์–ด๋””์„œ๋“  ํ•™์Šต

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์™„๋ฃŒ๊นŒ์ง€ 2๊ฐœ์›”

์ฃผ 2-3์‹œ๊ฐ„

์–ธ์ œ๋“  ์‹œ์ž‘

๋Œ€๊ธฐ ๊ธฐ๊ฐ„ ์—†์Œ

๊ณผ์ • ์„ธ๋ถ€์‚ฌํ•ญ

  • Medical Device Regulations (FDA, EU MDR/IVDR, etc.)
  • Quality Management Systems (ISO 13485, 21 CFR Part 820)
  • Risk Management (ISO 14971)
  • Design Controls
  • Post-Market Surveillance & Vigilance
  • CAPA (Corrective and Preventive Actions)
  • Auditing & Inspections
  • Documentation & Record Keeping
  • Regulatory Affairs
  • Human Factors Engineering

๊ฒฝ๋ ฅ ๊ฒฝ๋กœ

Job Role Description Regulatory Affairs Specialist (Medical Devices) Ensure compliance with UK and EU medical device regulations (MDR, IVDR).

Manage submissions and documentation.

Quality Assurance Manager (Medical Devices) Oversee quality systems, audits, and CAPA processes to maintain compliance standards within medical device manufacturing.

Compliance Auditor (Medical Devices) Conduct internal and external audits to verify compliance with regulatory requirements.

Identify and report non-conformances.

Clinical Affairs Specialist Support clinical evaluations and post-market surveillance activities for medical devices, ensuring compliance with regulations.

Medical Device Compliance Consultant Provide expert advice and guidance to medical device companies on regulatory compliance strategies and best practices.

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์™œ ์‚ฌ๋žŒ๋“ค์ด ๊ฒฝ๋ ฅ์„ ์œ„ํ•ด ์šฐ๋ฆฌ๋ฅผ ์„ ํƒํ•˜๋Š”๊ฐ€

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์ƒ˜ํ”Œ ์ธ์ฆ์„œ ๋ฐฐ๊ฒฝ
CAREER ADVANCEMENT PROGRAMME IN MEDICAL DEVICE COMPLIANCE
์—๊ฒŒ ์ˆ˜์—ฌ๋จ
ํ•™์Šต์ž ์ด๋ฆ„
์—์„œ ํ”„๋กœ๊ทธ๋žจ์„ ์™„๋ฃŒํ•œ ์‚ฌ๋žŒ
London School of International Business (LSIB)
์ˆ˜์—ฌ์ผ
05 May 2025
๋ธ”๋ก์ฒด์ธ ID: s-1-a-2-m-3-p-4-l-5-e
์ด ์ž๊ฒฉ์ฆ์„ LinkedIn ํ”„๋กœํ•„, ์ด๋ ฅ์„œ ๋˜๋Š” CV์— ์ถ”๊ฐ€ํ•˜์„ธ์š”. ์†Œ์…œ ๋ฏธ๋””์–ด์™€ ์„ฑ๊ณผ ํ‰๊ฐ€์—์„œ ๊ณต์œ ํ•˜์„ธ์š”.
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