Technical Writing and Document Management
Venue: Toronto
Event Date/Time: Sep 23, 2008 | End Date/Time: Sep 24, 2008 |
Description
- GMP, GLP Requirements and Regulatory Expectations for SOPs
- The SOP’s Role within a Quality Management System
- Auditing of SOP Compliance
- Performing a GAP Analysis of SOP Systems
- Minimizing SOP Review and Approval times
- Electronic vs Paper-Baed Document Mangement Systems
- Electronic Approval and Electronic Access
- Change Control of your SOPs
- Managing the Preparation of SOPs
- SOP Formats vs. other Document Formats
- Integrating SOPs with other Documents
- Writing Techniques for Effective Instruction
- Controlling Sequence of Actions
- Determine target audience, how SOPs will be used
- Assessing SOP Quality and Effectiveness
With Interactive Exercises on::
- Determining SOP Requirements
- Classifying Documents and SOPs
- Critiquing SOP Quality