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 Trainer, Dr Jennifer Thompson, has over 20 years of experience in the pharmaceutical sector in computer systems validation and IT infrastructure controls and compliance and has delivered projects for a wide range of companies in the UK, EU and USA including GlaxoSmithKline, Novartis Healthcare, Lonza Biologics, Elan Pharmaceuticals, Hoffman LaRoche and others. Her experience covers computerised systems used in manufacturing, laboratories, enterprise systems and clinical trials management. She has written articles and given presentations on a wide range of topics and contributed to the GAMP® Good Practice Guide “A Risk-based Approach to GxP Process Control Systems” and “The Risk Based Compliance Handbook” by Siegfried Schmitt (Paraxel).

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