Training Course:Root Cause Investigation for CAPASchool/Trainer:The Center for Professional Advancement
East Brunswick, New Jersey, United States
Course Format: Classroom | E-learning | Virtual Class | Online | On-site | Blended | Self-paced
Course Description:
'' Most organizations have procedures for implementing corrective and preventive actions, but many do not have an effective methodology to actually investigate to find the root cause. As a result the investigation is often careless, unsuccessful, and costly. Root Cause Investigation for CAPA is a proven methodology to investigate and identify the root cause when there has been a shift in the performance of a product, machine, equipment, work process, or system. The methodology identifies the change (or changes) that has occurred so that the change can be eliminated and the performance can return to its previous level. It is ideal for Product or service defect levels
Customer complaints
Negative patient reactions with the product
Manufacturing scrap or rework
Equipment or process aberrations
Any performance change where a CAPA investigation is required
This workshop, intensive course is designed to develop the skills necessary so that you can conduct an effective investigation immediately upon returning to your job. ...''
Please go to the school's official website for training price and schedule:
http://www.cfpa.com
Phone:(732)238-1600
School Address:
Corporate Office
Box 7077, 44 West Ferris Street
East Brunswick, NJ USA 08816-7077
Phone: (732)238-1600
Fax: (732)238-9113
Email info@cfpa.com
Europe Office
Oudezijds Voorburgwal 316A, 1012 GM
Amsterdam, The Netherlands
Phone +31/20/638.28.06
Fax +31/20/620.21.36
Email amsterdam@cfpa.com
Jobs & Resumes: East Brunswick
Houses & Roommates: East Brunswick
Other training courses offered by The Center for Professional Advancement:
Risk Analysis & Human Factors Engineering
Gums and Hydrocolloids
Microencapsulation and Particle Coating
Documentation Management and Control
Analytical Methods Validation for FDA Compliance
Drug Product Stability and Shelf-Life
Microbiological Control and Validation
Process Validation for the Pharmaceutical and Medical Device Industry
Non-Clinical Drug Safety Evaluation and Drug Development
ADME: Absorption, Distribution, Metabolism and Elimination
Complaint Procedures for Medical Devices
Early Stage Clinical Studies for Drugs and Devices
Drug Delivery Technologies
Drug Specifications for APIs and Drug Products
The Quality System
Good Clinical Practices (GCP)
Generic Drug Approvals
Generic Drug Approvals
Good Clinical Practices (GCP)
Notice: The course description on this page was captured from the Internet as historical reference or submitted by visitors. It was archived statically and not updated from day to day.
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