19th WRIB
Event details
Date: | April 7, 2025 - April 11, 2025 |
Website: | https://www.wrib.org/ |
Location: | New Orleans, LA, USA |
The 19th WRIB (Workshops on Recent Issues in Bioanalysis) will be built on the success of the previous meetings, especially the 18th WRIB where over 1100 professionals (in person and remote) representing pharma/biotech companies, CROs, and multiple regulatory agencies convened to discuss current topics of interest in bioanalysis. High Quality, better compliance to regulations and scientific excellence have always been the foundations of WRIB.
Each year WRIB program provides you with novel case studies and emerging approaches because it is the only program built on White Paper recommendations/consensus from the previous years to ensure no repetitions of same discussions but a continuous evolution of Science & Regulations & Technology applications.
19th WRIB will take place on April 7-11, 2025 in New Orleans, LA, USA. In case you are not sure about travel, remote attendance option will also be made available, and you can switch between the in-person and remote options.
19th WRIB will present again the best and most comprehensive program of the year with the most innovative scientific talks from industry leaders and the latest advice from regulators (with WRIB traditional interactive regulators’ sessions) to provide you with the best learning, interacting, and networking opportunity!
Upcoming Important Deadlines:
- Advance Registration Deadline: December 1, 2024
- Poster Abstract Submission Deadline: February 7, 2025
What makes WRIB special?
In this busy and fast paced environment, it is great to attend a conference that organizes everything for you so all you need to do is to focus on your learning:
- No need to look for speakers’ slides before and during the meeting… At WRIB you will still receive a printed program book containing all the presentation slides from all the speakers, so you can follow the talks and take notes on the slides in your program book where they belong to;
- No need to run to look for a restaurant/cafe for food and drinks… At WRIB, breakfast, mid-morning snacks, hot buffet lunch, mid-afternoon snacks, wine and beer reception drinks are all included for you every single day so you can just focus on learning and networking :-)
- No need to look for which session to follow or scramble from one room to another to catch different speakers in parallel sessions… At WRIB all sessions are sequential so just sit, relax, and enjoy the meeting!
Meet the Largest Panel of Regulators…
19th WRIB continues its traditional interactive Regulators’ Sessions including Regulators’ Inputs Presentations and “ASK THE REGULATORS” Panel Discussions with the Largest Panel of Regulators from the Globe to discuss Bioanalysis, Biomarkers, Immunogenicity, Gene Therapy, Cell Therapy and Vaccines!
Participating Regulators at the 19th WRIB again includes all Major and Influential Regulatory Agencies in North America, Europe, Latin America, and Asia Pacific.
Maximize your Learning…
19th WRIB continues to feature the unique 3-DAY Main Workshop sequential program including Main Workshop DAY 1, DAY 2 and DAY 3 for those aiming for full immersion in Bioanalysis.
However, for those into certain focus, there is the flexibility to select 2-DAY Main Workshop program by choosing either 2-DAY Ligand-binding, Cell-Based, and Molecular Assays (DAY 1 & DAY 2) or 2-DAY Mass Spec, Chromatography, and Sample Prep (DAY 2 & DAY 3) based on each attendee’s specific field of interest and learning needs.
In addition to the 3-DAY Main Workshop program, there are also 7 Full-Day Specialized Workshops dedicated for advanced training and specific focus spreading throughout the week to further deepen attendees’ knowledge with many choices to combine Main Workshop DAYs with these Specialized Workshops to maximize the learning process.
Come with your Questions, and go back with your Answers!
Like the previous editions, 19th WRIB will again be
- Very practical with a variety of hot topics/contents;
- Highly interactive with thought-provoking Q&A dialogs and panel discussions;
- Very informative with the active participation from global regulatory agencies;
- Well formulated with excellent balance of science and regulations.