Attend this webinar by expert speaker Danielle DeLucy, MS, to know how you can write, organize and maintain SOPs and also train your staff/personnel effectively to ensure reproducible and easy-to-follow compliance.

Governed by FDA and world health authorities, (SOPs) are industry regulatory requirements. When used in combination with planned training and regular performance feedback, SOPs facilitate an effective and motivated workforce. It is obvious that most people want to do a good job. A manager is successful when he/she can channelize the efforts of workers towards positive business development. If the SOPs are written well enough, they tend to improve communication, provide direction and improve consistency at work. Developing the SOP process is a good way for managers/technical advisers and workers to cooperate for everyone’s benefit.

Course Objectives:

You will learn how you can develop an effective review and approval process which will be compliant with regulatory requirements. Also, know how to implement a training program for document review and creation. In addition, learn how to format SOPs and provide a system for control, archival and disposal of written procedures.

Why Should You Attend:

Currently, no guidance is available on how to manage or develop the SOP creation or quality system. This leads to SOPs written so complicated and erroneous that compliance becomes difficult and sometimes impossible. Many cases have led to production of subpar documents which have come to light during a regulatory inspection.

Attend the webinar to know why written procedures and beneficial and understand the FDA expectations for regulatory requirements and written documents.

Course Outline:

• Why written procedures are beneficial
• FDA expectations for written documents and regulatory requirements
• Developing an effective review and approval process compliant with regulatory requirements
• How to implement a training program for document creation and review
• A system for the control, archival, and disposal of written procedures
• Formatting SOPs
• Elements to include other than the procedure
• How to write effective but efficient documents
• Roles and responsibilities of authors and reviewers of SOPs
• How to define roles in SOPs for supervisors and operators

What You Get:

• Training Materials
•  Live Q&A Session with our Expert
•  Participation Certificate
•  Access to Signup Community (Optional)
•  Reward Points

Who Will Benefit:

• Quality Systems Specialists
• Document Control Specialists
• Quality and Compliance Specialists
• Internal Auditors and Managers
• Training Specialists
• CAPA Specialists
• Supplier Quality Engineers and Auditors
• Quality/Compliance managers or directors for Medical Device companies
• Directors, Managers
• Professionals
• Technical writers and General staff with the responsibility for creating, reviewing and approving written standard operating procedures and instructions