ICMED 13485 Issue 2 Medical Devices Quality Management System (MDQMS) - Lead Implementer Course

- Description
- Curriculum

ICMED 13485 scheme is intended to enhance patient safety, and provide enhanced consumer protection along with much needed product credentials to manufacturers for instilling confidence among buyers. ICMED 13485 certification intends to significantly eliminate trading of sub-standard products or devices of doubtful origins in the market. ICMED 13485 certification also aims to bring down the substantial time and cost-run to obtain globally accepted quality certification for companies. ICMED 13485 standards is based on a number of quality management principles including a strong customer focus, the motivation and implication of top management, the process approach and continual improvement. An effective implementation is essential if organizations are to maximize the cost saving, performance, and customer satisfaction benefits of ICMED 13485 standards. ICMED 13485 lead implementer course is good for those who need an overview on the ICMED 13485 standards, or those who will be involved in the implementation of ICMED 13485 standards within an organization. ICMED 13485 implementation course will guide you through the implementation process by explaining the requirements of ICMED 13485 and how they can be applied using international best practices. Using a step-by-step approach, you will learn how to develop an implementation plan, create the necessary documentation, monitor the quality management system, and achieve continual system and quality improvement.
Who Should Attend?
- Anyone responsible for implementing ICMED 13485 standard
- Those who want to learn how to interpret the requirements of ICMED 13485 standard
- Managers or executives involved in delivering ICMED 13485
- Heads of various departments in an organisation
- Jobseekers interested in understanding the best quality management practices followed by the organizations in the medical device value chain
- Anyone looking to gain skills and knowledge in ICMED 13485
Key Benefits
- Understand concepts and importance of the ICMED 13485 management system principles.
- Grasp the application of risk-based thinking, leadership and process management
- Interpret requirements of ICMED 13485 standard and its effective application for managing and improving the functioning of an organization through process approach.
- Understand and develop skills for implementation of management system to manage processes of the organization.
- Build stakeholder confidence by managing processes in line with the latest requirements
- Understand and develop problem solving skills
- Maintain and continually improve your quality management system
- Learn techniques to create and manage documents and records relevant to ICMED 13485 quality management system , critical to the products and services delivered and those required to meet customer and regulatory requirements
- Learn skills in human resource management, supplier management, customer management , operations management, inventory management, laboratory management, production planning and logistics management to ensure compliance to ICMED 13485 medical device quality management system
- Learn to identify and mitigate internal and external quality issues relevant to businesses
- Learn to identify stakeholder expectations and prepare action plans to fulfill them
- Learn to define and optimize the processes in your organisation
- Understand the methods to develop a customer focus approach in an organisation
- Identify improvement objectives and plans to achieve them
- Understand traceability requirements relevant to products and services
- Develop an effective business communication plan
- Learn to manage design and development activities
- Learn techniques to manage nonconformity in products and services delivered and take corrective actions
- Fill gaps in your professional knowledge
Learning & Evaluation Method
This is a live and interactive course. Once you purchase the course, our team will contact you to plan the training. No matter where you are located, we schedule the classes based on your convenience and time zone. You can plan to attend the training in sessions of 4 or 8 hr duration, based on how much time you can spend in a day.
Certification
There are increasing numbers of organizations, who prefer candidates those who have certain certifications from recognized programs. Certification demonstrates your commitment to superior professionalism, upholding industry standards, and continued learning. These merits can help boost your professional credibility and prestige within your own network, in your organisation, with your current clients, and when pursuing new business opportunities. After the successful completion of the course and final exam, you will be awarded with a certificate of completion issued by QGlobal. Your credentials will be made available in the global online directory and can be verified by anyone searching with the certificate number. Without doubt we can say that our training courses are well recognized and sought after by organizations across various geographies.
Buy for group Are you planning to buy this course for a group? We have the best prices for you! Select ‘Buy for Group’ option and add to the cart. You will get a discount of 60 – 75% for a group of up to 10 participants. To make a group purchase, create your group name and add individual emails of up to 10 participants. Each participant will get the access to the course materials, exam and the certificate. We will arrange one live-online session for the entire group.
Total: 206 Courses View all
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1Introduction to standards and certification
- Purpose of standardization
- Benefits of certification
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2Introduction to ICMED Issue 2 standards
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3ICMED 13485 Quality management systems
- General requirements
- Documentation requirements
- Quality manual
- Medical device file
- Control of documents
- Control of records
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4ICMED 13485 Management responsibility
- Management commitment
- Customer focus
- Quality Policy
- Planning
- Quality objectives
- Quality management system planning
- Responsibility, authority and communication
- Responsibility and authority
- Management representative
- Internal communication
- Management review
- General
- Review input
- Review output
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5ICMED 13485 Resource management
- Provision of resources
- Human resources
- Infrastructure
- Work environment and contamination control
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6ICMED 13485 Product realization
- Planning of product realization
- Customer-related processes
- Determination of requirements related to product
- Review of requirements related to product
- Communication
- Design and development
- Design and development planning
- Design and development inputs
- Design and development review
- Design and development verification
- Design and development validation
- Design and development transfer
- Control of design and development changes
- Design and development files
- Purchasing
- Purchasing process
- Purchasing information
- Verification of purchased product
- Production and service provision
- Control of production and service provision
- Cleanliness of product
- Installation activities
- Servicing activities
- Particular requirements for sterile medical devices
- Validation of processes for production and service provision
- Particular requirements for validation of processes for sterilization and sterile barrier systems
- Identification
- Traceability
- Customer property
- Preservation of product
- Control of monitoring and measuring equipment
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7ICMED 13485 Measurement, analysis and improvement
- General
- Monitoring and measurement
- Feedback
- Complaint handling
- Reporting to regulatory authorities
- Internal audit
- Monitoring and measurement of processes
- Monitoring and measurement of product
- Control of nonconforming product
- Actions in response to nonconforming product detected before delivery
- Actions in response to nonconforming product detected after delivery
- Rework
- Analysis of data
- Improvement
- General
- Corrective action
- Preventive action
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8LI 01 Building the team
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9LI 02 Conducting gap analysis
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10LI 03 Preparing implementation plan
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11LI 04 Creating awareness
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12LI 05 Conducting training
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13LI 06 Procuring documents
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14LI 07 Creating management system manual
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15LI 08 Creating policies and procedures
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16LI 09 Creating forms and templates
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17LI 10 Planning for certification
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18Implementing ICMED 13485 standards