
Explore how a quality management system standardizes processes across a company—from training and inspection to manufacturing—ensuring FDA and ISO compliance, KPI-driven performance, and risk management per ISO 14971.
Define risk as the probability and severity of harm to people, property, or environment, and capture hazards within a quality management system to reduce risk in medical devices and pharmaceuticals.
Explore risk management basics: identify, analyze, and reduce hazards in medical devices and processes, using living risk management documents, process fmea, design fmeas, fall tree analysis, and regulatory considerations.
Classes of medical devices, as defined by different regulatory bodies are defined. Also explained the differences between ISO Clean room class and medical device classes.
Know about the rules and guidance set by Health Canada QMS for medical device. QMS Standard made public by Health Canada has been attached for reference. Students are required to check the latest version of standards before use.
Know about the rules and guidance set by US Food and Drug Administration for medical device. Attachment is a printed from taken directly from FDA website, open to public. Students are required to check the latest version of standards before official use.
ANVISA does not seem to publicly put out standards so standard document is not attached.
Please visit EU official website for latest guidance and standards for EU 2017/745 (MDR) and EU 2017/746 (IVDR)
Please visit Japan's official website for latest guidance and standards on PMDA MHLW MO 169 standards.
Know about the rules and guidance set by Therapeutic good Association of Australia for medical device. Attached document is a public document provided by Australian for Risk Management Activities. Students are required to check the latest version of standards before use.
Please visit ISO's official website for the preview of ISO 13485 standardstandards.
Please visit ISO official website (linked) to preview the overview of standards
Attached is the PFMEA template that I created from scratch. Sharing this template as reference.
Refer to the template provided on PFMEA lecture to be utilized for practice and reference.
Benefits and Disadvantage of using FMEA, PHA and Fault tree analysis (FTA) is discussed to help you understand which document is right for your organization.
Learn how to control the risk arising from process, design, tools and more in order to reduce risk to as low as possible.
What to with the residual risk after risk control measures have already been placed.
Learn about post market surveillance (PMS) methods and how to use PMS data as an input into RM activity to make your RM process more robust and updated.
Learn the role of top management in Risk Management Activity and how to proceed is risk outweighs the benefit from the medical device
Explore the four phases of hazard analysis in a hazop study—definition, preparation, examination, and documentation—and learn to define scope, assign responsibilities, and record actions for risk mitigation.
Explore how guide words in hazop studies use what-if questions to reveal deviations in process and design, applying risk controls with examples like rubber band length and water quality.
Assess the advantages and disadvantages of Hazop analysis as a non-quantitative brainstorming tool that captures hazards from human performance, while lacking risk ranking and cross-system interaction.
The most extensive course on Risk Management available in Udemy!
This course is designed to teach you everything that you need to know to become a Subject Matter Expert (SME) in Risk Management and Quality Management System (QMS) within Medical device, pharmaceutical industry and any other enterprise that conducts risk management activity.
Regardless of your current skills and experience, after taking this course, you will be comfortable communicating to experts in medical device industry about Quality management systems (QMS) and risk management (RM) standards and regulations.
By the end of this course you will be a pro at creating complex Risk Assessment and Risk Measurement documents such as PFMEA, DFMEA, HACCP, HAZOP, Benefit-Risk Analysis, Post Market Surveillance Report (PMSR), Clinical Effects Analysis Report (CEA) from the scratch! Knowing this skills will set you apart from the crowd and you can easily land you six-figure jobs in a reputed medical device companies.
You will be well versed in rules, regulations and standards for medical device industries across the world such as ISO14971 (Risk Management, ISO) , ISO13485, ISO 22000, 21CFR810 (FDA, USA), RDC 40/2015 (Anvisa, Brazil), EU 2017/745 MDR, MHLW MO 169 (PMDA, Japan) and TGR 2002 (TGA, Austrialia) and be able to talk about them in meetings, interviews and even with auditors.
You will learn how processes like complaint reviews, Corrective and Preventative Maintenance (CAPA), Process Validation (PV), Equipment Qualification (IQ/OQ/PQ) ties into Risk Management and why companies need to do these activities.
Whether you are just getting into Risk Management, or wants to freshen up your skills, or are looking to advance your career in the field, this course can provide you with more than enough knowledge to be the top 5% in your organization.
Note: This course is directly related to and applies to Enterprise Risk Management (ERM). Medical device and Pharmaceutical companies are an enterprises themselves so this course teaches you everything you need to know to manage risks in an enterprise. In fact, you will learn risk management in so much in-depth from this course that you can tackle risk management activities on any enterprise.
Note: This course also ties into Financial Risk Management (FRM) as we go in depth on the types of risks companies deals with, and financial risk is one of them. Hence students wanting to learn FRM can also greatly benefit from this course.