Online Training 2015 - The Controls for Outsourcing Manufacturing and Testing - By Compliance Global Inc
Date2015-11-12
Deadline2015-11-12
VenueOnline Webinar, USA - United States
KeywordsControls for Outsourcing; Compliance training; Regulatory consulting
Topics/Call fo Papers
Speaker: Howard T Cooper
Overview
"The Controls for Outsourcing Manufacturing and Testing" explores the use of outsourcing and how it impacts quality and compliance and the organization as a whole. The primary stakeholders and outsourcing include Quality, Research, Production, Laboratories, Purchasing/Procurement, Finance, and Senior Management.
This webinar will study the outsourcing lifecycle and its impact on the organization. Although outsourcing as a whole will be studied, the emphasis will be on contracting manufacturing, design, and testing.
The webinar will begin with a brief review about the importance of quality systems and their role in maintaining the organization. Outsourcing will be defined and examples throughout the FDA approved industry will be discussed. Of course, regulatory compliance requirements will be discussed to include the FDA's current thinking about the required controls. Particular emphasis will be given on the importance of understanding the differences between contractors and suppliers.
The process of auditing and qualifying contractors and assuring compliance quality goals are maintained, will be explained.
Why Should You Attend
This webinar will help you understand your responsibilities when outsourcing so that the product maintains its integrity and quality and satisfies customer and user requirements.
The FDA is closely scrutinizing these activities to assure that responsibilities outlined in the regulations and guidance is clearly defined between the contractor and its client.
These industry requirements are given in CFR Part 211.22(a), ICH Q7A 2.22-8, ICH Q7A 16, ICH-Q10 and Part 820, Subpart E.
The FDA has begun to more closely scrutinize the control of outsourcing because they have observed a frequent pattern where the firms allow contractors to completely control QA responsibilities.
Areas Covered in this Webinar
? The Resourcing Lifecycle
? The Quality Agreement-Defined Responsibilities
? Design and Change Control
? Maintaining Control and Problem solving
? Post-approval aspects of Outsourcing
? Quality Improvement and Resourcing
? Covering the loopholes
Learning Objectives
? Defining and Analyzing the Outsourcing Environment
? Regulatory Requirements For Outsourcing - Drugs & Devices
? Outsourcing Management
Who Will Benefit
? Regulatory Affairs Personnel
? Purchasing, Procurement, Outsourcing Department Staff
? R&D Professionals
? Quality Professionals
? Senior Management
Level:
Beginner
For more detail please click on this below link:
https://complianceglobal.us/product/700228
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Overview
"The Controls for Outsourcing Manufacturing and Testing" explores the use of outsourcing and how it impacts quality and compliance and the organization as a whole. The primary stakeholders and outsourcing include Quality, Research, Production, Laboratories, Purchasing/Procurement, Finance, and Senior Management.
This webinar will study the outsourcing lifecycle and its impact on the organization. Although outsourcing as a whole will be studied, the emphasis will be on contracting manufacturing, design, and testing.
The webinar will begin with a brief review about the importance of quality systems and their role in maintaining the organization. Outsourcing will be defined and examples throughout the FDA approved industry will be discussed. Of course, regulatory compliance requirements will be discussed to include the FDA's current thinking about the required controls. Particular emphasis will be given on the importance of understanding the differences between contractors and suppliers.
The process of auditing and qualifying contractors and assuring compliance quality goals are maintained, will be explained.
Why Should You Attend
This webinar will help you understand your responsibilities when outsourcing so that the product maintains its integrity and quality and satisfies customer and user requirements.
The FDA is closely scrutinizing these activities to assure that responsibilities outlined in the regulations and guidance is clearly defined between the contractor and its client.
These industry requirements are given in CFR Part 211.22(a), ICH Q7A 2.22-8, ICH Q7A 16, ICH-Q10 and Part 820, Subpart E.
The FDA has begun to more closely scrutinize the control of outsourcing because they have observed a frequent pattern where the firms allow contractors to completely control QA responsibilities.
Areas Covered in this Webinar
? The Resourcing Lifecycle
? The Quality Agreement-Defined Responsibilities
? Design and Change Control
? Maintaining Control and Problem solving
? Post-approval aspects of Outsourcing
? Quality Improvement and Resourcing
? Covering the loopholes
Learning Objectives
? Defining and Analyzing the Outsourcing Environment
? Regulatory Requirements For Outsourcing - Drugs & Devices
? Outsourcing Management
Who Will Benefit
? Regulatory Affairs Personnel
? Purchasing, Procurement, Outsourcing Department Staff
? R&D Professionals
? Quality Professionals
? Senior Management
Level:
Beginner
For more detail please click on this below link:
https://complianceglobal.us/product/700228
Email: referrals-AT-complianceglobal.us
Toll Free: +1-844-746-4244
Tel: +1-516-900-5515
Other CFPs
- How to Contest IRS Penalty and Interest Determinations and a Guide to Taking Cases to Appeals - By Compliance Global Inc
- Leadership Intelligence: How to Use Your Power and Influence Effectively - By Compliance Global Inc
- 3rd International Symposium on Advanced Web and Mobile Applications (AWMA 2016)
- 2nd International Workshop on Data-driven Self-regulating Systems (DSS 2016)
- 3rd International Workshop on Mobile Applications (MobiApps 2016)
Last modified: 2015-10-13 19:06:05