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Medical device Training


Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
Sep 20-21, 2021 The seminar will provide attendees with a better understanding of responsibilities and gain a greater knowledge of the issues faced
David R. Dills David R. Dills
$1,299
Full Day Virtual Workshop Qualification (IQ, OQ, PQ) and Validation of Laboratory Equipment and Syst
On 21 September 2021 This webinar will aim at understanding and scoping out various phases of Qualification activities that will be integrated
Joy L. McElroy Joy L. McElroy
$695
Tips for setting up a Quality System to withstand FDA Audits for Medical Device and Pharmaceutical Companies
05 Oct This webinar will provide a step by step approach and valuable tips for setting up a Quality System to withstand FDA Audits
Meena Chettiar Meena Chettiar
$199
Purchasing Controls, Supplier Management, and Receiving Acceptance for Medical Devices
Oct 14-15 , 2021 This 2-day virtual seminar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe
Susanne Manz Susanne Manz
$1,295
How FDA trains its investigators to review CAPA and what should you do to prepare
14 Oct This webinar will discuss all the documents used by FDA to train their inspectors to review your CAPA system, some of which you may not be familiar
Jeff Kasoff Jeff Kasoff
$299
21 CFR Part 11 and Annex 11; what you need to know to pass the new regulatory inspections
19 Oct Download This webinar describes exactly what is required for compliance with Part 11 and the European equivalent Annex 11 for local, SaaS/Cloud hosted
David Nettleton David Nettleton
$199
Calculations for Process and Product Capability
21 Oct This Webinar will focus on providing the information needed for attendees to know the appropriate measures and formulas
Elaine Eisenbeisz Elaine Eisenbeisz
$249
Production and Process Controls for Medical Devices What You Need to Know
21 Oct This webinar can help you prevent serious issues such as these. You’ll learn about FDA quality system regulation expectations, and how you can
Susanne Manz Susanne Manz
$487
A Comprehensive View of Medical Device Post-Market Regulations and Challenges During COVID-19— Complaint Handling, MDR Reporting and Recalls
Oct 21 - 22 this course will explain how to comply with complicated Complaint Handling, MDR and Recall requirements. Earl Bird. Register.
Rita Hoffman Rita Hoffman
$1,498
A Comprehensive View of Medical Device Post-Market Regulations and Challenges During COVID-19— Complaint Handling, MDR Reporting and Recalls
On 21-22-Oct, 2021 this course will explain how to comply with complicated Complaint Handling, MDR and Recall requirements. Earl Bird. Register.
Rita Hoffman Rita Hoffman
€1.295
Learn the Latest FDA Compliance and Mobile Applications Live Webinar
02 Nov This topic is focused on the use of mobile applications to process data regulated by FDA. These applications may be used to collect, analyze, transfer
Carolyn Troiano Carolyn Troiano
$199
Supervising a Human Error Free Environment: You can do a Lot More than you Think
04 Nov How can we prevent human error? This 90 -minutes online course will discuss why supervision is so important in reducing and preventing human error
Ginette Collazo Ginette Collazo
$179
FDA Recalls - Before You Start, and After You Finish
On 08 - 09 Nov, 2021 this seminar will help you to Understand FDA's recall authority and policy , Learn how to manage recalls under FDA oversight.
Kelly Thomas Kelly Thomas
$6,000
Excel Spreadsheet Validation-Step-by-step guide to data integrity compliance
17 Nov This session will make you a better Excel user, saving you time and costs
David Nettleton David Nettleton
$199
Purchasing Controls and Receiving Acceptance for Medical Devices
02 Dec This webinar can help you understand your responsibilities in terms of Purchasing Controls enabling you to provide safe and effective products
Susanne Manz Susanne Manz
$229
Computer System Validation Professional Certification Program 3 Days
Dec 08-09 3 day CSV course will teach you how to comply with key FDA and international CSV regulations and guidance, such as 21 CFR Part 11 and Annex 11.
Carolyn Troiano Carolyn Troiano
$1,599
3 Hrs Webinar on What You Need to Know: Investigating Out-of-Specification (OOS)
MP3 Download This webinar will review the regulatory requirements for investigating an OOS Investigation.
Danielle DeLucy Danielle DeLucy
$399
Post Market Surveillance - Complaint Handling and Medical Device Reporting
MP3 Download This webinar will cover the basics of complaint management and medical device reporting
Susanne Manz Susanne Manz
$229
Risk Based Verification and/or Validation to meet US FDA CGMP and ISO 13485 Requirements
MP3 Download This Webinar will provide valuable assistance to all regulated companies that need to review and modify their Master Validation Planning.
John E Lincoln John E Lincoln
$199
FDA’s Ambitious Regulation of Social Media - New Course By FDA Investigator
MP3 Download This webinar teach us about social media platforms provide common ways to cross FDA’s legal boundaries for “misbranding” your product
Casper (Cap) Uldriks Casper (Cap) Uldriks
$229
Hypothesis Testing, p-values, and Inference: When Thinking Like a Statistician Makes Sense
MP3 Download You will learn the why and how of the scientific method, and how to view the world with a statistician’s eyes
Elaine Eisenbeisz Elaine Eisenbeisz
$499
Multiplicity: When and How to Adjust for Multiple Testing
MP3 Download this webinar will explain the differences between family wise error rate (FWER) and false discovery rate (FDR).
Elaine Eisenbeisz Elaine Eisenbeisz
$249
Medical Device Cybersecurity and FDA Compliance
MP3 Download This webinar will focus on cybersecurity of medical devices, a key concern for those who develop, manufacture, test, and distribute these products
Carolyn Troiano Carolyn Troiano
$695
Audits in the World of COVID-19 and Beyond: Are You Ready for Remote Audits?
MP3 Download The presentation will provide an insight and guidance to managers with QA departments to implement a Remote Auditing program
Michael Ramcharan Michael Ramcharan
$229
What do the FDA, EMA and PMDA Look for When Conducting cGMP Regulatory Inspections
MP3 Download This webinar will cover the key areas of how ICH Q7 was established, it's goals and objectives, expectations of the healthcare authorities
Kelly Thomas Kelly Thomas
$499
US FDA Medical Device QSR, 21 CFR 820 and Quality Management System
MP3 Download Learn the basic overview of the original medical device Quality Management System
John E Lincoln John E Lincoln
$229
Elements of a Corrective and Preventive Action (CAPA) Program and Uses of CAPA Data
MP3 Download this webinar will cover all the items listed above, and more. If you want to improve your CAPA system, you cannot afford to miss this.
Jeff Kasoff Jeff Kasoff
$199
Quality by Design for Medical Devices Live Webinar
MP3 Download This webinar can help you create a design control process that is a competitive strength for your company.
Susanne Manz Susanne Manz
$699
The FDA Inspection: Best Practices for Preparation, Behavior, and Response
MP3 Download This course provides medical device/pharmaceutical professionals with the information they need to prepare for and manage any type of FDA
Jeff Kasoff Jeff Kasoff
$179
Risk-Based Approach to Part 11 Compliance and Policies and Procedures to Support GxPs
MP3 Download This webinar will help you understand in detail Computer System Validation (CSV) and how to apply the System Development Life Cycle
Carolyn Troiano Carolyn Troiano
$392
Purchasing Controls, Receiving Inspection, and Supplier Audit – what to do during a global pandemic
MP3 Download This webinar will provide insights into how to use remote auditing techniques to minimize the risk and maximize the benefits of conducting audits
Susanne Manz Susanne Manz
$199
FDA Regulation of Artificial Intelligence/ Machine Learning
MP3 Download This webinar is not a programming course but will explain the present and future regulatory requirements for AI/ML
Edwin Waldbusser Edwin Waldbusser
$265
Lifecycle Management of Analytical Methods and Procedures - according to new FDA and USP guidelines
MP3 Download This 2-day seminar will explain the new Analytical Procedure Lifecycle guidelines and give attendees the knowledge needed to implement recommend
Kelly Thomas Kelly Thomas
€1.295
How to write SOP's that Avoid Human Error
MP3 Download This Webinar will discuss the primary cause of quality and production losses in many industries
Ginette Collazo Ginette Collazo
$199
Identifying Sources of Process Unreliability Within Your Organization: You May be Surprised.
MP3 Download In this Webinar you will learn how to use Reality-Charting, The Model for Improvement, and Process Reliability Modeling
David W. Husman David W. Husman
$209
Dealing with CAPA- Corrective and Preventive Actions in FDA Regulated Industries
MP3 Download New Root Cause Analysis Techniques and CAPA Management live webinar is for those in Operations, Facilities , Engineering and QA/QC
Meena Chettiar Meena Chettiar
$179