Live Informative Sessions - Join Us!

The experts at QPharma will be giving some presentations towards the end of the year - and we want you to join us! We hope you have found our blog to be informative, interesting, and at times, entertaining. Come meet the subject matter experts who write our articles at the following venues:

October 24-27: 2010 RAPS Annual Meeting - San Jose, California

Come join Nancy Tomoney at our Sponsor Spotlight Session on Monday, October 25th! Nancy will be giving an informative learning session on:

Current Events Impacting FDA Registration and Sale for Products Marketing Through CDRH, CDER, CBER and CVM. 

QPharma is also giving away a Flip Video Camcorder - just stop by our Booth #525 and enter for your chance to win!

October 25-27: IVT'S Validation Week - Philadelphia, PA

Session 4, Day 2 - Tuesday October 26th Gregg Mauriello and Elise Miner are headed to Philadelphia, PA to give their talk on: Best Practices for Validation of a Software as a Service (SaaS) Customer Relationship Management (CRM) Solution. One of our most popular blog posts, this duo will be answering your questions on this process and addressing your most pressing concerns when it comes to validation "in the cloud".

Check out the description of their Session Track here (scroll to "Session 4").

November 7-10: ISPE 2010 Annual Meeting - Orlando, FL  

Nancy will be joined by Kim Stanton, another of QPharma's Validation Managers, at ISPE's meeting in Orlando this year. Our experts will be giving the following presentations on November 8th, 7:00 AM - 8:00 AM on Stage 2:

- Case Study in Good Laboratory Control Practices - Applying GAMP, Calibration Management, Good Laboratory Control and Good Engineering Practices for a Successful Move. 

Talk will detail the tasks, checklists, and activities used to relocate an Analytical Laboratory from one operating site location to another.  

- Applying Best Practices using Validation Test Management Tools for Validating Computer Systems.

Presentation will detail the efficiencies of Test Management Tools and how to apply best practices to Test Management tools to meet regulatory standards for Validation deliverables.

Visit us at our Booth #415 to talk to our Subject Matter Experts!

We hope to see you there!