Course offering number:1203-205
Course ID:
2435
Strategies for Setting up and Implementing Supplier Audits
March 7-8, 2012
New Brunswick, NJ
Who Should Attend
This intensive, practical two-day course will be of value to
those professionals in the pharmaceutical, medical device and
related industries who are responsible for or involved in any
interaction with suppliers, including those working in:
• Management
• Laboratories
• Auditing
• Purchasing
• QA/QC
• Procurement
• R&D
• Legal
• Manufacturing
• Validation
• Regulatory Affairs
• Documentation Management
Description
Outsourcing represents a critical and complex process
involving many parties and covering many geographical areas.
This process has become a global phenomenon.
This practical course will outline details of the outsourcing
process in the FDA regulated industries with emphasis on the
critical aspects of monitoring and preserving the integrity of
the supply chain. The importance and use of risk
management techniques will be presented.
The course will present the latest industry approaches and
practices in setting up and implementing supplier audits and
will discuss concrete steps to be taken by companies all
over the world, when implementing this program. Case
studies and group hands-on workshops will give participants
an opportunity to brainstorm and create real life documents.
Save $400 off combined regular tuition!
Attend this course and its companion course:
Documentation Management and Control
March 5–6, 2012 • New Brunswick, NJ • Course ID #1866