How to Write SOPs Training

The How to Write SOPs Training Course can be delivered in a hotel, one of our offices, your premises or online via a virtual classroom. The course content can be tailored to meet your requirements. Request a quote for an onsite or online course for an agreed number of delegates from your site.

Have you been asked to create and write a Standard Operating Procedure (SOP)? Are you a newcomer to SOPs, never written one or had to use one before? Seems a bit daunting doesn’t it?

The How to Write SOPs Training Course aims to provide you with the fundamental skills and knowledge to create effective SOPs.

Why are SOPs considered to be crucial for a company’s business processes? If you work in manufacturing and your company commits to producing a quality product or service; constructive SOPs covering critical tasks provide a method to ensure your Quality Management System is followed.

We suggest you do not leave it to chance, and take the time and opportunity to learn effectively how to dissect a task down into a logical structure and sequence, write the SOP and test it in use before approval.  Why not attend our course below?

• Understand the need for SOPs
• Why have and use Standard Operating Procedures?
• Understand what key features constitute an SOP
• Why some SOPs are difficult to understand, use and are not readily accepted by the users
• What makes an effective SOP?
• Defining where SOPs fit within a Quality System
• How SOPs fit in with other documentation
• How to control and manage SOPs
• Create a simple process flowchart
• Break down a task into logical steps
• Create a flowchart from the logical steps
• Provide a flowchart as the first part of a SOP
• Create a Standard Operating Procedure
• Use the flowchart to create a Standard Operating Procedure
• Review the SOP for potential improvements
• Training and SOPs
• The importance of training to SOPs
• Different training documents to use

This course can be delivered to a group of up to 12 delegates at your premises or as an online virtual classroom course for an agreed number of delegates from your site. Request a quote.

ITS’ Regulatory Compliance Services’ Manager, Elizabeth Vaughan, has developed extensive knowledge of this specialist area from over 30 years’ industry experience working with Sanofi, Bristol Myers Squibb, Diomed Developments and Vifor Pharma UK. Elizabeth has worked in quality roles within the laboratory and pharmaceutical industry, and gained extensive experience in global quality systems and regulatory affairs, as well as ISO 13485, ISO 9001 and cGMP compliance. Throughout her career, she has been responsible for sharing her knowledge through the design and delivery of a range of training courses for production personnel including Good Manufacturing Practice, Change Control, Deviation Management, Electronic Record Compliance, Validation and Management of API Suppliers/Manufacturers. Elizabeth also has extensive experience in providing quality and GMP training to improve the performance of site quality managers.

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