A Webinar for GMP professionals

How to Write an SOP That People Would Love to Follow


Wednesday, May 05, 2021
10:00-12:00 CEST, Berlin

Speaker: Yogesh K. Davé 

Every GMP professional must write or review SOPs at some point in their career.

Unfortunately, most people don’t know how to do it correctly, as they didn’t get proper training in writing simple, effective, and compliant SOPs. The result is poorly worded procedures and unpleasant opposition from colleagues.

Besides the emotional stress, inadequate SOPs lead to deviations, scrapping of batches, recalls, and compliance issues.

In this webinar, you will learn how to write excellent SOPs that are user-friendly and GxP compliant.

First Class Educator

Learn from an industry leader with 40+ years of experience in the field.

Engaging & Fun Learning

Forget about slides full of text!
We implement visual storytelling that will keep you attentive throughout the whole session.

High Information Retainability

Our teaching techniques will make sure you remember more from the lecture and can use your new skills at your workplace!

Virtual Classroom

See and communicate with the speaker, and other delegates live. Feel as if you are in the same room, as we welcome the use of webcams.

What you'll learn

Determining who is the best person to write the SOP

Using a multistep framework that will guarantee effective SOPs

Implementing unique "filters" to create simple and straightforward documents

15 expert tips that will make sure you have an excellent and compliant written procedures system

8 tips for SOP simplification

Examples of bad vs. good SOPs


Yogesh Krishan Davé

Yogesh has been a GxP consultant for about 12 years at his own limited company registered in the UK.

He has 40+ years’ experience in the pharmaceutical and biotech industries and is registered and eligible to perform the duties of an EU Qualified Person for Investigational medicinal products (IMPs) and medicines that have a full marketing authorization.

Before becoming an independent consultant, Yogesh held senior positions as Site Quality Director in several Pharma and Biotech companies and was the Senior Director for Clinical Trial Supplies and QP for a global full-service CRO based in the UK.

He has a comprehensive understanding of drug research, drug development, clinical research, and commercial manufacturing. He is also a trained lead auditor in GMP/GDP compliance and is knowledgeable on the ICH E6 (R2) GCP.

In this video, Yogesh explains how you can achieve a unified sense of responsibility for quality across the organization:

Still not sure if this webinar is for you? Take a look at what previous attendees have to say about it:

Why people love our Online GMP training

GMP is a serious matter and can be complicated. At Qualistery, we specialize in simplification! 

We present complicated matters in fun and engaging matter which captivates the audience.
The biggest complaint of our customers is that our training is “too short,” because they don’t notice the time fly! 

As a result, the attendees are more attentive and retain more information, which they can use to boost compliance and improve KPIs. 

In essence, we avoid the “Death by Powerpoint” phenomenon, by minimizing text and implementing visual storytelling in our training.

In other words, we approach each training as if it was a work of art!


Seats are limited.
Time slots choosable during checkout.

Silver Seat

Best for veteran professionals
€ 55 Excl. VAT
  • Live session
  • Q&A

Golden Seat

Best for career development
€ 85 Excl. VAT
  • Live session
  • Q&A
  • Certificate of attendance
  • Presentation copy (post event)

Diamond Seat

Best for subject matter experts
€ 125 Excl. VAT
  • Live session
  • Q&A
  • Certificates of attendance
  • Presentation copy (post event)
  • Recording (30 days unlmited viewing)

* Prices are per delegate


Most frequent questions and answers

Yes! You will be able to see the trainer and communicate with him/her. You could use the chat function or raise your hand and speak through your microphone.

We use Zoom Meetings to simulate a real class! You will be able to see the speaker, other delegates and communicate with them.

You will get your individual access link no later than 48 hours before the live session. If you book closer to the live session, you will get the access link immediately after payment. 

If you didn’t get your link up to 48 before the live session, please contact us at service@training.qualistery.com. We are quick to respond! 

The quickest way to contact us on the day of the event is to use our website’s live chat. See the chat bubble on the right? We will be there live at your service to make sure everything goes smoothly for you.

Alternatively, you can message us at info@training.qualistery.com.

We highly recommend you use your webcam and leave it on throughout the session. This will contribute to the “together” feeling and help the speaker see your reaction and adjust himself.

Please keep your microphone on mute during the session unless you raised your hand and given permission to talk by the hosts. 

Please wear headphones to avoid echo and disturbances when you use your microphone. 

IMPORTANT: Please note that the session is recorded, and you agree to that when you choose to turn on your webcam and use the microphone to communicate. 

About Us

Qualistery GmbH is a company dedicated to providing engaging, live online training for GMP professionals. Our teaching approach replaces the conventional text training with captivating visual storytelling. We believe that learning GMP should be exciting and fun. Additionally, this approach increases the effectiveness of the lessons and helps you with material retainability.

Wait, don't leave empty-handed!​

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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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