3-Hour Virtual Seminar on SOP Writing, Training and Compliance in the Pharmaceutical Industry 2019

3-Hour Virtual Seminar on SOP Writing, Training and Compliance in the Pharmaceutical Industry 2019 is dedicated to standard Operating Procedures (SOPs) as the basis for a large part of the day-to-day training in the pharmaceutical industry.

Topics

• Regulatory requirements for SOPs
• What commitments you make when you put your process in writing
• Using process excellence tools to create a robust process and procedure
• Consequences of noncompliance
• Keeping training in mind while writing procedures
• How your foundation keeps subsequent steps from going awry
• Define the parameters of an effective SOP
• What identifies a poorly written procedure
• Why poorly written procedures have a negative impact on production
• Interact with the SOP process owner/author to improve the writing of procedures
• Compliance risks with ambiguity or excessive detail
• Relationship between SOPs and employees training curricula
• Integrate the SOP effectively into the position curricula of employees
• Retention of the content at the training stage
• Why the training department needs to be in the loop at the start of the SOP development process
• Perform an ongoing assessment of knowledge retention of SOPs for continuous improvement
• The implications of good training for successful SOP execution
• Review of learning objectives
• Avoid pitfalls in revising SOPs

Who should Attend

Attendees from:

• Quality Departments
• Compliance Departments
• Production Departments
• R & D Departments
• Engineering Departments
• Management – essentially everyone in the organization who is tasked with creating or reviewing procedures
• IT Departments