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Develop and Implement Procedures that Survive the Lifecycle

December 4-6, 2017
  • Philadelphia, PA

The laboratory landscape continues to face an influx of regulations surrounding the reliability, consistency and accuracy of analytical methods and data. From FDA’s final guidance on analytical procedures to USP chapter updates to FDA and MHRA’s determination to enforce action on data integrity, the demand for attention to compliance detail has never been greater.

Whether your responsibilities include method development, method validation, method verification or method transfer, IVT’s 3-day laboratory-focused event — Analytical Procedures & Methods Validation — will provide a comprehensive understanding of global regulatory trends and requirements, “hands-on” training for executing procedures that survive the lifecycle, and solutions to top challenges of complying with today’s expanded FDA CDER requirements.

Join your colleague this December and go beyond just theory to gain practical examples, tools, SOPs, templates and knowledge to ensure regulatory excellence in your analytical lab.

NEW THIS YEAR!

BYOC — Bring Your Own Challenge Workshop

Practical Applications for Critical Method Validation Procedures

Lina Patel, PhD
Director, Quality Operations Bio-Analytical Laboratory
Merck Manufacturing Division

Office Hours!

Gain insights on your individual laboratory and method validation challenges by meeting one-on-one with Lab Week speaking faculty.

Engage in 17 Interactive Courses and
Critical Discussions, Including:

  • Regulatory Snapshot — Update on Guidances in Analytical Methods,
    Stability Testing and Lifecycle Laboratory Management
  • Mitigating Data Integrity Risk in Analytical Methods & Stability Testing
  • Lifecycle Management in the Laboratory
  • Industry Pulse on Emerging Regulatory Trends and Warning Letters —
    FDA, MHRA, USP and Beyond
  • Implement and Optimize an Effective Method Transfer Strategy
  • Writing Master Validation Plans

Triple the Content. Triple the Network. Triple the Value.

Your Analytical Procedures and Methods Validation registration grants you access to IVT’s full Lab Week event. Comprised of three unique conference experiences — Analytical Procedures & Methods Validation, Stability Testing and Laboratory Data Integrity — IVT’s Lab Week series is designed to maximize your time out of the office, providing the value of three conferences in one.

Download the Lab Week Preview

Previous Attendee Acclaim:

Great, enthusiastic and convincing speakers!

Supervisor, Abbott

Great opportunity to listen to Method Validation subject matter experts and network with scientists in
similar fields. Highly recommend.

Research Chemist, ECBC

Great conference for analytical chemists!

Associate Chemist II, Upsher-Smith Laboratories

Analytical Procedures & Methods Validation

Develop and Implement Procedures that Survive the Lifecycle

The laboratory landscape continues to face an influx of regulations surrounding the reliability, consistency and accuracy of analytical methods and data. From FDA’s final guidance on analytical procedures to USP chapter updates to FDA and MHRA’s determination to enforce action on data integrity, the demand for attention to compliance detail has never been greater.

Whether your responsibilities include method development, method validation, method verification or method transfer, IVT’s 3-day laboratory-focused event — Analytical Procedures & Methods Validation — will provide a comprehensive understanding of global regulatory trends and requirements, “hands-on” training for executing procedures that survive the lifecycle, and solutions to top challenges of complying with today’s expanded FDA CDER requirements.

Join your colleague this December and go beyond just theory to gain practical examples, tools, SOPs, templates and knowledge to ensure regulatory excellence in your analytical lab.

NEW THIS YEAR!

BYOC — Bring Your Own Challenge Workshop

Practical Applications for Critical Method Validation Procedures

Lina Patel, PhD
Director, Quality Operations Bio-Analytical Laboratory
Merck Manufacturing Division

Office Hours!

Gain insights on your individual laboratory and method validation challenges by meeting one-on-one with Lab Week speaking faculty.

Engage in 17 Interactive Courses and
Critical Discussions, Including:

  • Regulatory Snapshot — Update on Guidances in Analytical Methods,
    Stability Testing and Lifecycle Laboratory Management
  • Mitigating Data Integrity Risk in Analytical Methods & Stability Testing
  • Lifecycle Management in the Laboratory
  • Industry Pulse on Emerging Regulatory Trends and Warning Letters —
    FDA, MHRA, USP and Beyond
  • Implement and Optimize an Effective Method Transfer Strategy
  • Writing Master Validation Plans

Triple the Content. Triple the Network. Triple the Value.

Your Analytical Procedures and Methods Validation registration grants you access to IVT’s full Lab Week event. Comprised of three unique conference experiences — Analytical Procedures & Methods Validation, Stability Testing and Laboratory Data Integrity — IVT’s Lab Week series is designed to maximize your time out of the office, providing the value of three conferences in one.

Download the Lab Week Preview

Previous Attendee Acclaim:

Great, enthusiastic and convincing speakers!

Supervisor, Abbott

Great opportunity to listen to Method Validation subject matter experts and network with scientists in
similar fields. Highly recommend.

Research Chemist, ECBC

Great conference for analytical chemists!

Associate Chemist II, Upsher-Smith Laboratories