+32 10 46 10 10 info@arlenda.com

December 4-6, 2017

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.

Do you have a question? Visit the event website.

Event Dates

Monday, December 4, 2017 –
Wednesday, December 6, 2017

Location

Hilton Philadelphia at Penn’s Landing
201 S. Christopher Columbus Boulevard
Philadelphia, PA 19106, USA