New Seminars by ComplianceOnline - Sponsored posting

SOPs for FDA-Regulated Industry: Best Practices to Withstand FDA Expectations: 2-day In-person Seminar - Cambridge, MA June 20/21

Computer System Validation - Reduce Costs and Avoid 483s: 2-day In-person Seminar - San Francisco, CA  - June 20/21  and  Philadelphia, PA - Sept 26/27

The Sunshine Act - Have you seen the light? What you need to know to get prepared for August 1, 2013. The clock is ticking. Get prepared now, before it's too late! : One-day In-person Seminar - River North, IL June 21

Conducting Effective Investigation of Out-of-Specs and Atypical Laboratory Data: One and a Half day In-Person Seminar - Philadelphia, PA  July 11/12

A Comprehensive View of FDA Regulations for Medical Devices: 2 - Day In-Person Seminar - Boston, MA July 30/31 

Understanding and Implementing the Medical Device Directive: 2-Day In-person Seminar - Boston, MA Aug 1/2

Root Cause and Root Cause Analysis and Out-Of-Specification (OOS) Training: 2-day In-person Seminar - London, UK Aug 15/16

Latin America: Regulatory Compliance Requirements for Life Science Products (Focus: Brazil, Mexico, Argentina): 2-day In-person Seminar - Philadelphia, PA Aug 22/23

GMP Compliance for Quality Control and Contract Laboratories: 2-day In-person Seminar - San Diego, CA Aug 26/27

Analytical Instrument Qualification and System Validation: 2- day In-person Seminar - Cambridge, MA Aug 29/30