Executive Development Programme in Device Recall Strategy
-- ViewingNowThe Executive Development Programme in Device Recall Strategy is a certificate course designed to address the growing need for professionals skilled in managing device recalls in the medical device industry. This programme emphasizes the importance of effective recall strategy, compliance, and risk management, making it highly relevant for professionals in this field.
2,475+
Students enrolled
GBP £ 149
GBP £ 215
Save 44% with our special offer
ě´ ęłźě ě ëí´
100% ě¨ëźě¸
ě´ëěë íěľ
ęłľě ę°ëĽí ě¸ěŚě
LinkedIn íëĄíě ěśę°
ěëŁęšě§ 2ę°ě
죟 2-3ěę°
ě¸ě ë ěě
ë기 ę¸°ę° ěě
ęłźě ě¸ëśěŹí
⢠Device Recall Overview: Understanding the basics of device recall, its impact on the organization, and the role of an executive in managing it.
⢠Regulatory Compliance: Ensuring compliance with regulatory requirements for device recall, including FDA regulations and international standards.
⢠Risk Management: Identifying and assessing risks associated with device recall, and implementing strategies to mitigate those risks.
⢠Crisis Management: Developing and implementing a crisis management plan to respond to device recall incidents, including communication strategies and stakeholder management.
⢠Quality Management: Understanding the role of quality management in preventing device recall, including effective quality control and assurance processes.
⢠Supply Chain Management: Managing the supply chain during device recall, including coordination with suppliers, distributors, and customers.
⢠Financial Impact: Assessing the financial impact of device recall, including cost estimation, budgeting, and financial reporting.
⢠Stakeholder Management: Managing relationships with key stakeholders, including regulators, customers, and investors, during device recall.
⢠Lessons Learned: Analyzing the root causes of device recall, implementing corrective actions, and developing strategies to prevent future recalls.
ę˛˝ë Ľ 경ëĄ
- Product Compliance Manager: Responsible for ensuring that products meet regulatory and quality standards, managing the recall process, and implementing corrective actions.
- Quality Assurance Director: Oversees the quality assurance department, ensuring that all products adhere to the company's quality standards, and manages the recall process if necessary.
- Regulatory Affairs Specialist: Ensures that the company complies with all relevant regulations and standards, coordinates recalls when required, and communicates with regulatory bodies.
- Supply Chain Strategist: Optimizes the supply chain process, coordinates recalls when necessary, and implements strategies to mitigate future recall risks.
- Data Analyst: Analyzes and interprets data to identify patterns and trends, helping the organization make informed decisions regarding recall processes and preventive measures.
- Product Compliance Manager: ÂŁ50,000 - ÂŁ75,000
- Quality Assurance Director: ÂŁ70,000 - ÂŁ120,000
- Regulatory Affairs Specialist: ÂŁ40,000 - ÂŁ65,000
- Supply Chain Strategist: ÂŁ55,000 - ÂŁ90,000
- Data Analyst: ÂŁ30,000 - ÂŁ50,000
ě í ěęą´
- 죟ě ě ëí 기본 ě´í´
- ěě´ ě¸ě´ ëĽěë
- ěť´í¨í° ë° ě¸í°ëˇ ě ꡟ
- 기본 ěť´í¨í° 기ě
- ęłźě ěëŁě ëí íě
ěŹě ęłľě ěę˛Šě´ íěíě§ ěěľëë¤. ě ꡟěąě ěí´ ě¤ęłë ęłźě .
ęłźě ěí
ě´ ęłźě ě ę˛˝ë Ľ ę°ë°ě ěí ě¤ěŠě ě¸ ě§ěęłź 기ě ě ě ęłľíŠëë¤. ꡸ę˛ě:
- ě¸ě ë°ě 기ę´ě ěí´ ě¸ěŚëě§ ěě
- ęśíě´ ěë 기ę´ě ěí´ ęˇě ëě§ ěě
- ęłľě ě겊ě ëł´ěě
ęłźě ě ěąęłľě ěźëĄ ěëŁí늴 ěëŁ ě¸ěŚě뼟 ë°ę˛ ëŠëë¤.
ě ěŹëë¤ě´ ę˛˝ë Ľě ěí´ ě°ëŚŹëĽź ě ííëę°
댏롰 ëĄëŠ ě¤...
ě죟 돝ë ě§ëʏ
ě˝ě¤ ěę°ëŁ
- 죟 3-4ěę°
- 쥰기 ě¸ěŚě ë°°ěĄ
- ę°ë°Ší ëąëĄ - ě¸ě ë ě§ ěě
- 죟 2-3ěę°
- ě 기 ě¸ěŚě ë°°ěĄ
- ę°ë°Ší ëąëĄ - ě¸ě ë ě§ ěě
- ě 체 ě˝ě¤ ě ꡟ
- ëě§í¸ ě¸ěŚě
- ě˝ě¤ ěëŁ
ęłźě ě ëł´ ë°ę¸°
íěŹëĄ ě§ëś
ě´ ęłźě ě ëšěŠě ě§ëśí기 ěí´ íěŹëĽź ěí ě˛ęľŹě뼟 ěě˛íě¸ě.
ě˛ęľŹěëĄ ę˛°ě ę˛˝ë Ľ ě¸ěŚě íë