Writing Standard Operating Procedures (SOPs) the Right Way

This online interactive and engaging workshop will help you master the essential elements of writing standard operating procedures (SOPs) and instructions that are easy to understand and follow. Mastering this skill will allow you to make sure that any operation runs smoothly and efficiently.

Sessions:
13 -14 April 2021 (4 hours per day)
12 – 13 October 2021 (4 hours per day)

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For a pharmaceutical operation to run smoothly, people need to understand what they need to do to the smallest detail. That’s why we have the standard operation procedures (SOPs) in place. However, not everybody knows how to write SOPs that are clear, simple, and to the point. We have all encountered SOPs that are too long, unclear, and confusing. In such cases, many employees work according to their experience bases, best practices. However, when every person works differently, it is a recipe for disaster and will eventually lead to deviations and broken processes. Therefore, pharmaceutical quality professionals must master mastery, writing SOPs, and instructions that are clear and easy to follow.

This workshop covers the essential elements for writing SOPs for manufacturing, testing, control, and distribution of medicinal products. You will learn best practice frameworks for determining when you need an SOP or a Work Instruction and understand the difference between the two. Also, you will comprehend what is the imperative, mandatory tense, and how to use it. Additionally, you will learn how to manage your controlled document system.

By the end of this hands-on workshop, you will be able to write clear and effective SOPs that will take the operation at your workplace to a new level.

Topics

  • SOP vs. instructions
  • Overview of different types of SOP/instructions
  • Standard content
  • Writing styles
  • Documentation control
  • Implementation of the SOP system

Target Group

This course is of particular importance to pharmaceutical quality professionals in all GxP fields.

All systems used in pharmaceutical companies must have appropriate, clear instructions. This course will provide you with the essentials for writing SOPs that are clear without being wordy and confusing.

Event Details

The workshops last about 8 hours, spread across two days.
That way, you don't get overwhelmed with too much material at once. Also, you can get back to your urgent projects after launch.

Start time: 09:00 CET

End time: 13:00 CET

765

Plus 19% VAT

Limited Spots Available

Your Instructor

Alex Hall

QP Trainer & Consultant

Alex is an expert in Pharmaceutical Quality Assurance with 30 plus years in the pharma industry, 20 of those as a Qualified Person. As an instructor, Alex builds on her experience and her previous role as a UK QP Assessor to support QA professionals and QP trainees. She helps trainees achieve the best results through supportive coaching, mentoring, and a straightforward training approach.

You can learn more about Alex from her appearance on The Qualitalks Podcast:

1. When You Deal With Risk, Don’t Be a Firefighter!

2. The Role of the Qualified Person (QP)

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What People Say About Our GMP Online Training

Our online interactive workshops will be presented to you live through a specialized classroom platform. You will be able to attend from home or work, yet feel like we share the same room.

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GMP Training

Communication

See and communicate with the tutor through a webcam and chat

Interactions

Raise your virtual hand to ask questions

Activities

Partake in polls and quizzes

Teamwork

Participate in exercises with other delegates

Let us Know Your Needs

Please share with us several suitable dates for private training sessions and the number of attendees. We will get back to you with a customized offer as soon as possible. 

Wait, don't leave empty-handed!​

Download our free FMEA guide, which is dedicated to GMP and pharma professionals.

This extensive yet simplified guide to Failure Mode and Effects Analysis (FMEA) will help you master one of the most vital instruments in your risk management toolbox.

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