Writing Reports for Failure Investigations and Process Deviations
Who Should Attend
This introductory to intermediate-level course is designed for those responsible for investigating and documenting failures and deviations within the Pharmaceutical, Biotechnology and Medical Device industries. Specifically, the following professionals would benefit most from the course:-
QA/QC Specialists
-
QA/RA Managers
-
QA Auditors
-
Manufacturing Associates/Supervisors
-
Compliance Specialists
-
Validation Engineers/Scientists
-
Production Supervisors
-
Quality Systems Analysts
-
Scientists/Chemists
-
Documentation Specialists
-
Stability Engineer
-
Customer Relations and Product Surveillance Professionals
Booking Options
Booking Options:
- Register online or Call Customer Service - Tel: (866) 647-0921 or email register@pti-international.com
- Group Discounts (3 or more people for this course) - Call Johana Morales at (646) 895-7447 or email jmorales@iirusa.com
- Bring this Course to Your Facility (10 or more people or further customization) - Call (800) 303-8194 or email OnSiteSolutions@pti-international.com