Webinar Search Results : 9 Upcoming webinars found.
Susanne Manz Wednesday, August 22, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:3 Hours
Price: ¤290.00
by: Susanne Manz
3-Hour Virtual Seminar on CAPA for Medical Devices
CAPA is the foundation of an effective Quality Management System. Yet, many companies suffer from Death by CAPA - a slow, bureaucratic, and ineffective CAPA process. Not only do they fail to achieve necessary improvements, they waste precious time and resources. This 3-hour webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. Learn how to avoid common problems and establish an efficient and effective CAPA process leading to improved quality and compliance for your company.

Susanne Manz Thursday, August 30, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:90 Minutes
Price: ¤150.00
by: Susanne Manz
Preparing for an FDA Inspection - What you Need to Know
Although an effective Quality System should always be inspection ready, many medical device companies make basic mistakes during inspections leading to 483s and even warning letters. This webinar can help you manage inspections efficiently and effectively.

Susanne Manz Friday, August 31, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:3 Hours
Price: ¤290.00
by: Susanne Manz
3-Hour Virtual Seminar on Design Controls for Medical Devices
Design Control is considered a critical process by the FDA. Yet is still a common source of 483 and Warning Letter observations. Most importantly, Design Control is critical to product quality, ensuring safe and effective products for your customers.

Susanne Manz Thursday, September 6, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:90 Minutes
Price: ¤150.00
by: Susanne Manz
Death By CAPA - Does your CAPA Program Need a CAPA?
This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

Susanne Manz Thursday, October 4, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:90 Minutes
Price: ¤150.00
by: Susanne Manz
Secrets to Writing Effective SOPs for Medical Device QMS
Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

Susanne Manz Thursday, October 25, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:90 Minutes
Price: ¤150.00
by: Susanne Manz
Essentials of Validation - IQ, OQ, PQ
Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation. You'll learn about what processes needed to be validated and what steps you need to take to validate processes. You'll learn the essentials of validation planning, protocol writing, and change management

Susanne Manz Thursday, November 8, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:90 Minutes
Price: ¤150.00
by: Susanne Manz
Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices
This webinar will help you understand the critical ingredients for conducting an effective root cause analysis. You will learn about FDA expectations, tools and techniques, and tips for conducting and documenting root cause analysis. We will discuss the myths, challenges, and best practices for this critical process. We'll also cover the essentials of doing a failure investigation.

Susanne Manz Thursday, November 15, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:90 Minutes
Price: ¤150.00
by: Susanne Manz
Risk Management Techniques for Medical Devices
Product Risk Management is a critical aspect of ensuring medical devices are safe and effective for intended uses. This course will help you understand the regulatory requirements, including ISO14971, and how to create processes and procedures to implement them.

Susanne Manz Thursday, November 29, 2018
10:00 AM PDT | 01:00 PM EDT
Duration:90 Minutes
Price: ¤150.00
by: Susanne Manz
Addressing CAPA within a Device Quality System
This webinar will help you ensure an efficient and effective CAPA process leading to improved quality and compliance for your company. You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA this webinar is for you.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Secrets to Writing Effective SOPs for Medical Device QMS
    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

  • Susanne Manz Recorded
    View Anytime
    Price: ¤390.00
    by: Susanne Manz
    Secrets to Writing Effective SOPs for Medical Device QMS
    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

  • Susanne Manz Recorded
    View Anytime
    Price: ¤190.00
    by: Susanne Manz
    Addressing CAPA within a Device Quality System
    This webinar will help you ensure an efficient and effective CAPA process leading to improved quality and compliance for your company. You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA this webinar is for you.

  • Susanne Manz Recorded
    View Anytime
    Price: ¤390.00
    by: Susanne Manz
    Addressing CAPA within a Device Quality System
    This webinar will help you ensure an efficient and effective CAPA process leading to improved quality and compliance for your company. You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA this webinar is for you.

  • Susanne Manz Recorded
    View Anytime
    Price: ¤190.00
    by: Susanne Manz
    Risk Management Techniques for Medical Devices
    Product Risk Management is a critical aspect of ensuring medical devices are safe and effective for intended uses. This course will help you understand the regulatory requirements, including ISO14971, and how to create processes and procedures to implement them.

  • Susanne Manz Recorded
    View Anytime
    Price: ¤390.00
    by: Susanne Manz
    Risk Management Techniques for Medical Devices
    Product Risk Management is a critical aspect of ensuring medical devices are safe and effective for intended uses. This course will help you understand the regulatory requirements, including ISO14971, and how to create processes and procedures to implement them.

  • Susanne Manz Recorded
    View Anytime
    Price: ¤190.00
    by: Susanne Manz
    Death By CAPA - Does Your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Death By CAPA - Does Your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Quality is not an Organization
    What does Quality mean to you? Is it a noun meaning an attribute or characteristic measured against a standard or customer requirement? Is it a state of product being free from defects? Is it an organization within your company that is responsible for creating inspection standards or a quality system? Or is it something more? It can be something more powerful for your company. It can be a culture of excellence and a management philosophy leading to improved customer satisfaction and business success.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Quality is not an Organization
    What does Quality mean to you? Is it a noun meaning an attribute or characteristic measured against a standard or customer requirement? Is it a state of product being free from defects? Is it an organization within your company that is responsible for creating inspection standards or a quality system? Or is it something more? It can be something more powerful for your company. It can be a culture of excellence and a management philosophy leading to improved customer satisfaction and business success.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Essentials of Validation -IQ,OQ,PQ
    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation.You’ll learn about what processes needed to be validated and what steps you need to take to validate processes. You’ll learn the essentials of validation planning, protocol writing, and change management.We’ll cover the steps of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) including tips and best practices.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Essentials of Validation -IQ,OQ,PQ
    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation.You’ll learn about what processes needed to be validated and what steps you need to take to validate processes. You’ll learn the essentials of validation planning, protocol writing, and change management.We’ll cover the steps of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) including tips and best practices.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Secrets to Writing Effective SOPs for Medical Device QMS
    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Secrets to Writing Effective SOPs for Medical Device QMS
    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Addressing CAPA within a Device Quality System
    This webinar will help you ensure an efficient and effective CAPA process leading to improved quality and compliance for your company. You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA this webinar is for you.

  • Susanne Manz Recorded
    View Anytime
    Price: ¤390.00
    by: Susanne Manz
    Addressing CAPA within a Device Quality System
    This webinar will help you ensure an efficient and effective CAPA process leading to improved quality and compliance for your company. You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA this webinar is for you.

  • Susanne Manz Recorded
    View Anytime
    Price: ¤190.00
    by: Susanne Manz
    Essentials of Validation -IQ,OQ,PQ
    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation.You'll learn about what processes needed to be validated and what steps you need to take to validate processes. You'll learn the essentials of validation planning, protocol writing, and change management.We'll cover the steps of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) including tips and best practices.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Essentials of Validation -IQ,OQ,PQ
    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation.You'll learn about what processes needed to be validated and what steps you need to take to validate processes. You'll learn the essentials of validation planning, protocol writing, and change management.We'll cover the steps of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) including tips and best practices.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Quality is not an Organization
    What does Quality mean to you? Is it a noun meaning an attribute or characteristic measured against a standard or customer requirement? Is it a state of product being free from defects? Is it an organization within your company that is responsible for creating inspection standards or a quality system? Or is it something more? It can be something more powerful for your company. It can be a culture of excellence and a management philosophy leading to improved customer satisfaction and business success.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Quality is not an Organization
    What does Quality mean to you? Is it a noun meaning an attribute or characteristic measured against a standard or customer requirement? Is it a state of product being free from defects? Is it an organization within your company that is responsible for creating inspection standards or a quality system? Or is it something more? It can be something more powerful for your company. It can be a culture of excellence and a management philosophy leading to improved customer satisfaction and business success.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Essentials of Validation - IQ, OQ, PQ
    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation. You'll learn about what processes needed to be validated and what steps you need to take to validate processes. You'll learn the essentials of validation planning, protocol writing, and change management.We'll cover the steps of Installation Qualification (IQ),Operational Qualification (OQ), and Performance Qualification (PQ) including tips and best practices.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Essentials of Validation - IQ, OQ, PQ
    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation. You'll learn about what processes needed to be validated and what steps you need to take to validate processes. You'll learn the essentials of validation planning, protocol writing, and change management.We'll cover the steps of Installation Qualification (IQ),Operational Qualification (OQ), and Performance Qualification (PQ) including tips and best practices.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices
    This webinar will help you understand the critical ingredients for conducting an effective root cause analysis. You will learn about FDA expectations, tools and techniques, and tips for conducting and documenting root cause analysis. We will discuss the myths, challenges, and best practices for this critical process. We'll also cover the essentials of doing a failure investigation.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices
    This webinar will help you understand the critical ingredients for conducting an effective root cause analysis. You will learn about FDA expectations, tools and techniques, and tips for conducting and documenting root cause analysis. We will discuss the myths, challenges, and best practices for this critical process. We'll also cover the essentials of doing a failure investigation.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Death by CAPA - Does your Company have the Symptoms?
    CAPA is the foundation of an effective Quality Management System. Yet, many companies suffer from a slow, bureaucratic, ineffective CAPA process. Not only do they fail to achieve necessary improvements, they waste precious time and resources. This webinar will help you avoid those struggles and establish an efficient and effective CAPA process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Death by CAPA - Does your Company have the Symptoms?
    CAPA is the foundation of an effective Quality Management System. Yet, many companies suffer from a slow, bureaucratic, ineffective CAPA process. Not only do they fail to achieve necessary improvements, they waste precious time and resources. This webinar will help you avoid those struggles and establish an efficient and effective CAPA process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Non-Conforming Material and Failure Investigation
    Non-conforming material happens. And medical device companies must deal it. This 90-minute webinar will help you to make sense of confusing regulations and effectively deal with non-conforming material. You'll learn how to identify, segregate, control, and disposition non-conforming material. You'll learn about conducting failure investigations and requirements for correction and corrective action. Join industry expert, Susanne Manz from Manz Consulting Inc, to learn the essentials of dealing with non-conforming material.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Non-Conforming Material and Failure Investigation
    Non-conforming material happens. And medical device companies must deal it. This 90-minute webinar will help you to make sense of confusing regulations and effectively deal with non-conforming material. You'll learn how to identify, segregate, control, and disposition non-conforming material. You'll learn about conducting failure investigations and requirements for correction and corrective action. Join industry expert, Susanne Manz from Manz Consulting Inc, to learn the essentials of dealing with non-conforming material.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Secrets to Writing Effective SOPs for Medical Device QMS
    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Secrets to Writing Effective SOPs for Medical Device QMS
    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Essentials of Validation - IQ, OQ, PQ
    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation. You'll learn about what processes needed to be validated and what steps you need to take to validate processes. You'll learn the essentials of validation planning, protocol writing, and change management

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Essentials of Validation - IQ, OQ, PQ
    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation. You'll learn about what processes needed to be validated and what steps you need to take to validate processes. You'll learn the essentials of validation planning, protocol writing, and change management

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Quality is not an Organization
    What does Quality mean to you? Is it a noun meaning an attribute or characteristic measured against a standard or customer requirement? Is it a state of product being free from defects? Is it an organization within your company that is responsible for creating inspection standards or a quality system? Or is it something more? It can be something more powerful for your company. It can be a culture of excellence and a management philosophy leading to improved customer satisfaction and business success.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Quality is not an Organization
    What does Quality mean to you? Is it a noun meaning an attribute or characteristic measured against a standard or customer requirement? Is it a state of product being free from defects? Is it an organization within your company that is responsible for creating inspection standards or a quality system? Or is it something more? It can be something more powerful for your company. It can be a culture of excellence and a management philosophy leading to improved customer satisfaction and business success.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Secrets to Writing Effective SOPs for Medical Device QMS
    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Secrets to Writing Effective SOPs for Medical Device QMS
    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Non-Conforming Material and Failure Investigation
    Non-conforming material happens. And medical device companies must deal it. This 90-minute webinar will help you to make sense of confusing regulations and effectively deal with non-conforming material. You'll learn how to identify, segregate, control, and disposition non-conforming material. You'll learn about conducting failure investigations and requirements for correction and corrective action. Join industry expert, Susanne Manz from Manz Consulting Inc, to learn the essentials of dealing with non-conforming material.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Non-Conforming Material and Failure Investigation
    Non-conforming material happens. And medical device companies must deal it. This 90-minute webinar will help you to make sense of confusing regulations and effectively deal with non-conforming material. You'll learn how to identify, segregate, control, and disposition non-conforming material. You'll learn about conducting failure investigations and requirements for correction and corrective action. Join industry expert, Susanne Manz from Manz Consulting Inc, to learn the essentials of dealing with non-conforming material.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Preparing for an FDA Inspection - What you Need to Know
    Although an effective Quality System should always be inspection ready, many medical device companies make basic mistakes during inspections leading to 483s and even warning letters. This webinar can help you manage inspections efficiently and effectively.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Preparing for an FDA Inspection - What you Need to Know
    Although an effective Quality System should always be inspection ready, many medical device companies make basic mistakes during inspections leading to 483s and even warning letters. This webinar can help you manage inspections efficiently and effectively.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤340.00
    by: Susanne Manz
    3-Hour Virtual Seminar on Design Controls for Medical Devices
    Design Control is considered a critical process by the FDA. Yet is still a common source of 483 and Warning Letter observations. Most importantly, Design Control is critical to product quality, ensuring safe and effective products for your customers.

  • Susanne Manz Recorded
    View Anytime
    Duration:3 Hours
    Price: ¤540.00
    by: Susanne Manz
    3-Hour Virtual Seminar on Design Controls for Medical Devices
    Design Control is considered a critical process by the FDA. Yet is still a common source of 483 and Warning Letter observations. Most importantly, Design Control is critical to product quality, ensuring safe and effective products for your customers.

  • Susanne Manz Recorded
    View Anytime
    Duration:3 Hours
    Price: ¤340.00
    by: Susanne Manz
    3-Hour Virtual Seminar on CAPA for Medical Devices
    CAPA is the foundation of an effective Quality Management System. Yet, many companies suffer from Death by CAPA - a slow, bureaucratic, and ineffective CAPA process. Not only do they fail to achieve necessary improvements, they waste precious time and resources. This 3-hour webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. Learn how to avoid common problems and establish an efficient and effective CAPA process leading to improved quality and compliance for your company.

  • Susanne Manz Recorded
    View Anytime
    Duration:3 Hours
    Price: ¤540.00
    by: Susanne Manz
    3-Hour Virtual Seminar on CAPA for Medical Devices
    CAPA is the foundation of an effective Quality Management System. Yet, many companies suffer from Death by CAPA - a slow, bureaucratic, and ineffective CAPA process. Not only do they fail to achieve necessary improvements, they waste precious time and resources. This 3-hour webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. Learn how to avoid common problems and establish an efficient and effective CAPA process leading to improved quality and compliance for your company.

  • Susanne Manz Recorded
    View Anytime
    Duration:3 Hours
    Price: ¤190.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Death By CAPA - Does your CAPA Program Need a CAPA?
    This webinar will help you establish an efficient and effective CAPA (Corrective and Preventive Action) process leading to improved quality and compliance for your company. You'll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA, this webinar is for you. We will discuss requirements, the myths, and the challenges of managing CAPAs so you can avoid common problems and pitfalls.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Secrets to Writing Effective SOPs for Medical Device QMS
    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Secrets to Writing Effective SOPs for Medical Device QMS
    Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes resulting in correct outcomes and quality work.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Essentials of Validation - IQ, OQ, PQ
    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation. You'll learn about what processes needed to be validated and what steps you need to take to validate processes. You'll learn the essentials of validation planning, protocol writing, and change management

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Essentials of Validation - IQ, OQ, PQ
    Validation is an important element of the Quality System Regulations and ISO13485. This course will cover the requirements the essentials of validation. You'll learn about what processes needed to be validated and what steps you need to take to validate processes. You'll learn the essentials of validation planning, protocol writing, and change management

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices
    This webinar will help you understand the critical ingredients for conducting an effective root cause analysis. You will learn about FDA expectations, tools and techniques, and tips for conducting and documenting root cause analysis. We will discuss the myths, challenges, and best practices for this critical process. We'll also cover the essentials of doing a failure investigation.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Root Cause Analysis for CAPA - Myths, Challenges, and Best Practices
    This webinar will help you understand the critical ingredients for conducting an effective root cause analysis. You will learn about FDA expectations, tools and techniques, and tips for conducting and documenting root cause analysis. We will discuss the myths, challenges, and best practices for this critical process. We'll also cover the essentials of doing a failure investigation.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Risk Management Techniques for Medical Devices
    Product Risk Management is a critical aspect of ensuring medical devices are safe and effective for intended uses. This course will help you understand the regulatory requirements, including ISO14971, and how to create processes and procedures to implement them.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Risk Management Techniques for Medical Devices
    Product Risk Management is a critical aspect of ensuring medical devices are safe and effective for intended uses. This course will help you understand the regulatory requirements, including ISO14971, and how to create processes and procedures to implement them.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤190.00
    by: Susanne Manz
    Addressing CAPA within a Device Quality System
    This webinar will help you ensure an efficient and effective CAPA process leading to improved quality and compliance for your company. You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA this webinar is for you.

  • Susanne Manz Recorded
    View Anytime
    Duration:90 Minutes
    Price: ¤390.00
    by: Susanne Manz
    Addressing CAPA within a Device Quality System
    This webinar will help you ensure an efficient and effective CAPA process leading to improved quality and compliance for your company. You’ll learn how to streamline and monitor your process to ensure compliance and improved performance. If your CAPA process needs a CAPA this webinar is for you.

Payment Methods

Contact Us

NetZealous LLC,
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539, USA.

Information

  Refund Policy
  +1-800-447-9407
  support@compliance4All.com