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Webinar on Validation and Use of Excel® Spreadsheets in Regulated Environments

 
  March 04, 2016  
     
 


Compliance Trainings, Online
2016-03-22


Description :

Excel® Applications are widely used in laboratories, offices and manufacturing e.g., for data capture, data manipulation and report generation. Regulations such as HIPAA, Sarbanes Oxley Act and FDA's GxP and 21 CFR Part 11 require users of software and computer systems to demonstrate and document data accuracy, integrity and confidentiality. Out-of-the box Excel® has not been designed for regulated environments. However, with a good knowledge of Excel® capabilities combined with good procedures and practices on how to validate and use Excel® requirements can be met. For example, the FDA is widely using Excel® and complies with its own regulations.

For easy implementation, attendees will receive

SOP:  Validation of spreadsheet applications

SOP:  Development and use of spreadsheets in regulated environments

Gap analysis/checklist for Macros and Spreadsheet applications

Areas Covered in the Session :

Regulatory requirements for spreadsheets; FDA Part 11 and GxP

Recent FDA inspectional observations and warning letters

Recommendations from the new GAMP®5 and EU Annex 11

How to design spreadsheets for compliance.

How to design, ensure and validate spreadsheet integrity.

When, what and how much to test?

Validation of standard/native Excel functions?

How to apply risk based validation to spreadsheet applications

Validation of 'ad hoc' spreadsheet applications.

How to document planning, specifications, installation, testing and changes

Examples from manufacturing, laboratories and offices

Who Will Benefit:

Everybody developing and using Excel Worksheets for regulated environments

Developers and users of spreadsheet templates

Lab Supervisors and managers

QA managers and personnel

QC managers and personnel

IT managers and personnel

Analysts and lab managers

Validation groups

Training departments

Documentation department

Consultants

 

Teachers

 
 
Organized by: Compliance Trainings
Invited Speakers:

Ludwig Huber, Ph.D., is the director of Labcompliance and editor of (www.labcompliance.com), the global online resource for validation and compliance. He is the author of the books "Validation and Qualification in Analytical Laboratories" and "Validation of Computerized Analytical and Networked Systems". He has given multiple presentations mainly on GLP/GMP, 21 CFR Part 11, 21CFR Part 111 and Validation around the world. This included seminars, workshops and presentations for the US FDA, China SFDA, Korea MFDS, Singapore HSA, ISPE, Japan PDA, PIC/S and several other national health care agencies. For more information, please visit Dr.Huber's website (www.ludwig-huber.com).

 
Deadline for Abstracts: 2016-03-22
 
Registration:

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1764

 

To register this webinar

https://compliancetrainings.com/siteengine/Login.aspx 

E-mail: suzzane.d@compliancetrainings.com
 
   
 
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