Interphase Systems will be exhibiting at the 2010 PDA/FDA Joint Regulatory Conference on September 13-14, at the Renaissance Hotel in Washington, D.C.

The PDA/FDA Joint Regulatory Conference offers the unique opportunity for you to join FDA representatives and industry experts in face-to-face dialogues. Each year, FDA speakers provide updates on the current state of efforts impacting the development of global regulatory strategies; while industry professionals from some of today’s leading pharmaceutical companies present case studies on how they employ global strategies in their daily processes. Hear directly from FDA experts and representatives of global regulatory authorities, and take home best practices for compliance. You won’t find this level of direct information exchange with FDA at any other conference!

Take part in three dynamic learning tracks:
• Foundations: Get back to quality basics in times of change! Sessions will discuss CAPA, inspection management, recalls and quality unit responsibilities.

• Quality Today: Talk about the challenges facing today’s quality professionals including supply chain management, knowledge management and biologics.

• Merging and Emerging Issues: Focus on global regulations, merging quality systems, regulatory communication and foreign inspection practices.

Interphase Systems provides cost effective software products and solutions to meet your regulatory needs. Our risk based validations approach saves you time and money. Showcased products include Ready-CAPA (software to track issues, observations, incidents and improvements to meet regulatory requirements) and XLAuditTrail (to make your spreadsheets 21CFR Part11 compliant)

Come check us out at Booth #31!

Click here for more information on the PDA/FDA Joint Regulatory Conference or if you would like to Register