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4th Annual Medical Device Validation Week 2019

Tue, March 12 - Thu, March 14, 2019 Minneapolis, Minnesota
Courtyard by Marriott Minneapolis Downtown 1500 S Washington Ave Minneapolis, Minnesota 55454 United States +1 612-333-4646

About 4th Annual Medical Device Validation Week 2019

4TH ANNUAL MEDICAL DEVICE VALIDATION WEEK, MINNEAPOLIS, MARCH 12-14, 2019

IVT’s 4th Annual Medical Device Validation Week is the must-attend event for quality, validation and design control professionals in medical device and diagnostics companies to benchmark with industry leaders and peers to improve current validation practices.

This event covers critical topics including, risk management in validation and verification, data integrity, test method validation (TMV) and much more. Further, it will provide critical content on evolving regulatory landscapes in the United States and internationally. Benefit from strategies and techniques to achieve best in class verification and validation and tangible takeaways to elevate products and teams.

Compelling Content to Achieve Best-in-Class Validation:

  • Review Quality Management Systems (QMS) Implications of EU MDR
  • Hear an Update on FDA & Industry Collaboration on Computer Software Assurance
  • Address Common Challenges in Test Method Validation (TMV)
  • Advance Project Management Skills for the Validation Professional
  • Develop Effective Strategies for Managing Risk Throughout the Product Lifecycle
  • Discuss Key Challenges in Data Integrity and Technical Systems Qualification

Who should attend:

You will benefit from this conference if you are a manager, director or executive at a medical device company working in the following areas:

  • QA/QC
  • Validation
  • Process Verification
  • Design Verification and Validation
  • Engineering
  • Regulatory Affairs
  • Design Control
  • R&D
  • Compliance

 

About Medical Device Validation Week 2017

Medical Device Validation Week, March 28-30, 2017:

What is this event?

This conference gives concise training, in-depth strategy sharing and educational tools separated through two tracks, design control and process validation and verification.

Medical Device Validation Week 2017 is designed for quality, validation, verification and design control professionals to benchmark with industry leaders and investigators on improving current validation techniques and return to the office with actionable tactics to enhance productivity and maintain compliance.

Where is this event located?

This event will take place at Marriott Courtyard Minneapolis Downtown, 1500 South Washington Avenue, Minneapolis, MN, USA.

To make a reservation and receive IVT’s discounted hotel rate please call 1-877-699-3216 and be sure to mention IVT’s Med Device Validation.

Who should attend this event?

You will benefit from this conference if you are a manager, director or executive at a medical device company working in the following areas:

  • QA/QC
  • Validation
  • Process Verification
  • Design Verification and Validation
  • Engineering
  • Regulatory Affairs
  • Design Control
  • R&D
  • Compliance

What are some highlights of this event?

Event Highlights:

  • Evaluate the Global Regulatory Landscape for Medical Devices
  • Cultivate Your Vision for a Comprehensive Validation Procedure
  • Risk Management Mastery — Quick Guide to Preparing an Effective Risk Plan
  • Leverage FMEA to Improve Design Verification
  • How to Conduct Test Method Validation (TMV) for Medical Devices
  • Effectively Manage Change Control Processes Enterprise-Wide
  • Process Validation Policy Mini Masterclass
  • Senior-Level Think Tank — Best Practices to Maintain the Validated State
  • Test Method Validation of In-Vitro Diagnostic Products
  • Build a Site Master Validation Plan (MVP)
  • Discern Best Strategies to Handle and Minimize Variability

Speakers:

  • Timothy Carr
  • Dharmesh Rupareliya
  • Mihir Vashi
  • Roberta Goode, MSBE, CQE
  • George Omae
  • Kris Nowicki

Why should I attend this event?

By attending this event you will:

  • Ensure data security and data integrity through an effective CSV system.
  • Manage change control processes enterprise-wide.
  • Develop and utilize expedited SOPs.
  • Benchmark with colleagues to improve comprehensive validation practices.
  • Get opportunity to learn and share best practices and experiences across the industry.

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