Join QPharma in Philadelphia on May 18 – 19
Are you compliant with FDA requirements for process validation? Today’s regulators are applying more fine-grained specifications and demanding more sophisticated procedures for planning, executing, and documenting your processes throughout a drug product’s lifecycle. Join QPharma, FDA, and other industry experts for an intensive two-day conference on May 18 to 19, 2017 at the Racquet Club of Philadelphia, PA.
Jeff Boatman serves as Senior Subject Matter Expert of Medical Devices and Quality Systems at QPharma. A process validation expert, Jeff will deliver a presentation titled Process Validation: General Principles and Practices, and will clear up the confusion around process validation and the differences between the (sometimes conflicting) guidances issued by various divisions of the Food & Drug Administration.
Scott Collins is QPharma’s Director of Lab Compliance Practice, and has been with the company over 23 years. Scott is a seasoned Validation Subject Matter Expert, and he will give a presentation on the development of an effective and compliant Validation Master Plan for pharmaceutical, medical device, and a wide variety of and life sciences industry projects.
To learn more and register to attend, please review the Conference Brochure.
Mention QPharma to receive a $200 discount.