ICMED 13485 Issue 2 Medical Devices Quality Management System (MDQMS) - Awareness 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. ICMED 13485 Foundations course teaches you the process approach, quality management principles and the requirements and benefits of ICMED 13485. The essential objective of ICMED 13485 foundations course is to create awareness for participants regarding various basic requirements of the ICMED 13485 standard & impart working knowledge on how these requirements can be interpreted to suit the organization’s processes, products, people & customers.
Who Should Attend?
- Anyone involved in the planning, implementing, maintaining, supervising or auditing of an ICMED 13485 medical device quality management systems
- 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 medical device quality management system
Key Benefits
- Understand the structure of ICMED 13485 standard
- Learn importance and benefits of an ICMED 13485 quality management system
- Understand key requirements, terms and definitions of ICMED 13485
- Understand main concepts such as risk-based thinking, process approach, Plan-Do-Check-Act, and quality management principles.
- Prepare yourself to participate in ICMED 13485 standards implementation process
- Manage quality and drive continual improvement
- Take steps to ensure that quality is at the heart of your organization
- Attract and retain customers by meeting their current and future needs better
- Understand 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
- 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.
Sample Certificate
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: 205 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