LearningPlus adapts its courses to your firm's special needs and particular regulatory requirements. LearningPlus instructors present the course, which are generally one or two days in length.

• Improving Quality by Focusing on Human Error (NEW for 2007)
• FDA and GMP Update 2006/2007 (Updated)
• Introduction to Risk Assessment and Risk Management for the Pharma and BioPharma Industry
• Applying the cGMP Regulations
• cGMP Basics
• Documentation Systems and Practices
• Eighty-eight Reasons to Use the GMPs
• Evaluating Training Program Effectiveness
• GMP Auditing
• GMP Decision Making
• GMP Training Issues for QA Personnel
• Investigating Deviations
• Managing in a GMP Environment
• Procedures For Performance: Developing and Writing SOPs
• Supervisors, Managers, and the cGMPs
• Validation and Change Control Basics
  

You may download a list of courseware and workshops in a printer-friendly format.