SOPs 2015 - Systematic Approach To Writing Effective Standard Operating Procedures (SOPs)
Date2015-01-23
Deadline2015-01-23
VenuePalo Alto, USA - United States
KeywordsStandard Operating Procedures; SOPs; Code of Federal Regulations
Topics/Call fo Papers
This FDA compliant SOPs training will explain how to write, organize, and maintain Standard Operating Procedures (SOPs) and
train personnel so that you can ensure FDA compliance in a way that is concise, reproducible and easy to follow.
Why Should You Attend:
Standard Operating Procedures (SOPs) are required by law for companies that are regulated by the Code of Federal
Regulations such as Title 21 and Title 493. Yet there is no guidance on how to write, organize and maintain SOPs.
Consequently, SOPs are frequently written in a way that makes compliance difficult or downright impossible. Worse, this
often leads to many regulatory errors that first come to light during a FDA audit.
This webinar will instruct the participant on how to write, organize, and maintain SOPs and train personnel in a way that
will ensure compliance in a way that is concise, reproducible and easy to follow. The course will begin with a strategic
view of SOPs in a company and how SOPs can help streamline operations in addition to ensuring regulatory compliance. The
course instructor will offer guidance on how to get from regulations to the SOP. Finally, best practices for creating,
implementing and maintaining SOPs using a risk based approach and best practices for getting SOPs ready for inspection will
be presented.
Areas Covered in the Webinar:
SOPs and their relation to the regulations.
SOPs as part of the company's regulatory infrastructure.
SOP on SOPs and how to ensure conciseness, consistency and ease of use.
Risk based approach on SOP best practices for creation and maintenance.
Training on SOPs.
Tools for SOP tracking and when is validation required.
What the FDA looks for in SOPs during an inspection.
Who Will Benefit:
CEOs
Regulatory VPs
Quality VPs
IT VPs
Regulatory Affairs Professionals
Quality Managers
Quality Engineers
Small Business Owners
Consultants
Regulators
GxP Professionals
For Registration:http://www.complianceonline.com/writing-effective-...
train personnel so that you can ensure FDA compliance in a way that is concise, reproducible and easy to follow.
Why Should You Attend:
Standard Operating Procedures (SOPs) are required by law for companies that are regulated by the Code of Federal
Regulations such as Title 21 and Title 493. Yet there is no guidance on how to write, organize and maintain SOPs.
Consequently, SOPs are frequently written in a way that makes compliance difficult or downright impossible. Worse, this
often leads to many regulatory errors that first come to light during a FDA audit.
This webinar will instruct the participant on how to write, organize, and maintain SOPs and train personnel in a way that
will ensure compliance in a way that is concise, reproducible and easy to follow. The course will begin with a strategic
view of SOPs in a company and how SOPs can help streamline operations in addition to ensuring regulatory compliance. The
course instructor will offer guidance on how to get from regulations to the SOP. Finally, best practices for creating,
implementing and maintaining SOPs using a risk based approach and best practices for getting SOPs ready for inspection will
be presented.
Areas Covered in the Webinar:
SOPs and their relation to the regulations.
SOPs as part of the company's regulatory infrastructure.
SOP on SOPs and how to ensure conciseness, consistency and ease of use.
Risk based approach on SOP best practices for creation and maintenance.
Training on SOPs.
Tools for SOP tracking and when is validation required.
What the FDA looks for in SOPs during an inspection.
Who Will Benefit:
CEOs
Regulatory VPs
Quality VPs
IT VPs
Regulatory Affairs Professionals
Quality Managers
Quality Engineers
Small Business Owners
Consultants
Regulators
GxP Professionals
For Registration:http://www.complianceonline.com/writing-effective-...
Other CFPs
Last modified: 2014-12-21 23:05:50