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OOS investigations in a GMP environment

 
  February 08, 2015  
     
 
PharmCourses Ltd, London
2015-10-19


This course is designed to provide essential training for conducting Out of Specification (OOS) investigations in a GMP environment. A background discussion of the associated GMP documentation required to support the OOS investigation is included but the majority of time is spent detailing the who, what, when, how and why of the investigation, determining the extent of the investigation during Phase I and Phase II, documenting findings determining root causes and assigning corrective and preventative actions. An introduction to OOT (Out of Trend) results and an overview of the different types and how they are typically handled is also discussed using industry examples in the first session of this course.

This course is presented in a dynamic environment created by a power point presentation, interactive exercises, case studies and group discussion. Participants are welcome to bring their own examples for group discussion sessions.

The workshop emphasizes practical issues such as:

· What is an OOT?

· The importance of good quality support systems

· FDA audit observations and how they could have been avoided

· Case studies for OOS results

· A detailed guide to conducting Phase 1 and Phase II of the OOS investigation

· Reporting and evaluating passing and failing results

The course provides ample opportunities for group discussions, case studies and exercises. It enables participants to gain the skills and knowledge necessary to meet current regulatory expectations. The course material is based on the FDA guideline “Investigating Out-of-Specification (OOS) Test Results for Pharmaceutical Production”, October 2006

Who should attend

This Two-day course is valuable for Directors, Managers, Supervisors, Laboratory Analysts and Associates working in a GMP environment in the Pharmaceutical and related industries with daily responsibilities in the following areas:

· Quality Assurance

· Documentation and Technical Writing

· Quality Control Laboratory

· Regulatory Affairs

· Contract Laboratory

· Analytical Laboratory

· Project Management

· Training

 

 Programme available on our website 

 

 

 

 
 
Organized by: PharmaCourses Ltd
Invited Speakers: Dr Pauline McGregor
 
Deadline for Abstracts: .
 
Registration:

Early-bird fee: £1080.00 if booked and paid by 21 August 2015

Full Fee: £1200.00

E-mail: info@pharma-training-courses.com
 
   
 
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