Standard Operating Procedures 2022 - Seminar on Bad Standard Operating Procedures (SOPs) – Bad Training: Garbage In, Garbage Out

3-Hour Virtual Seminar on Bad Standard Operating Procedures (SOPs) – Bad Training: Garbage In, Garbage Out
Product Id : FDB3584
Category : Food, Drugs & Biologics, Information Technology, Quality, Virtual Seminars
Presenter : Michael Esposito
Scheduled On : March 07 2022 12:00 pm
US/Canada (Eastern Time - ET)
Duration : 3 Hours
Standard Operating Procedures (SOPs) are necessary to demonstrate compliance with regulations and operational practices. It also serves as a documented roadmap which ensures consistency. This is integral to a strong quality system. If you want to improve SOPs writing and training materials that create more effective training as well as help in the reduction of errors, this webinar is for you.
Learn to define the parameters of an effective SOP
How your foundation keeps subsequent steps from going awry-preventing “garbage in”
What interactions are necessary with the SOP process owner/author to improve the writing of procedures •
How can we translate the SOP into effective curriculum development and training execution
Considerations related to curricula and Learning Management Systems (LMSs) o Considerations for training: reading of SOPs with assessments and/or classroom training
Perform an ongoing assessment of the knowledge retention of learners for continuous improvement
Who Should Attend:
This course will be of benefit to anyone who is an owner of a process, responsible for writing or reviewing procedures, and/or managing training in a GMP environment.
Pharmaceutical industry- particularly those areas that develop SOPs for the manufacturing or quality monitoring of pharmaceutical products, which would also include Information Technology (IT) employees who manage systems training
Quality Departments
Production Departments
Compliance Departments
Engineering Departments
R & D Departments
Management – essentially everyone in the organization who is tasked with creating or reviewing procedures
Areas Covered in the Session :
Regulatory requirements for SOPs
Define the parameters of an effective SOP – how your foundation keeps subsequent steps from going awry – preventing “garbage in”
Why bad procedures have a negative impact on training
What identifies a bad procedure
Identify appropriate level of detail for document
How the training department needs to be in the loop at the start of the SOP development process
What SOP writers and approvers need to keep in mind for retention of the content at the training stage
Translate the SOP into effective curriculum development and training execution
The implications of good training for successful SOP execution
How the SOP wording can be “translated” into language that is appropriate for learners if a presentation, computer-based training or classroom session is to be developed
Perform an ongoing assessment of the knowledge retention of learners for continuous improvement
Use several different methods
Take advantage of tools that already exist in your organization
Review of learning objectives