How To Write An SOP That People Would Love To Follow

A Webinar for GMP professionals

Days

Hours

Minutes

Seconds

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

Speaker

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:

"I was looking for ways to improve our SOPs and decided to join the webinar by Qualistery. I've learned there about novel ideas, such as asking "why" about each step in the procedure to make sure we need it. By the end of the webinar, I got plenty of ideas on simplifying our company's SOPs. If you are involved in QA, you should not think twice about joining Qualistery's detailed training from key people with significant experience in the field - It's not a long time to set aside; you may just learn something new."

"I don't enjoy reading SOPs in general, and I always wanted to write so that people will enjoy them better. My biggest realization at the webinar was that people should use more images and photographs! Also, I love how Qualistery's webinars are always well prepared and informative and would suggest any QA professionals to join!"

"I joined Qualistery's webinar to learn better methods to write and simplify SOPs. I immensely enjoyed the speaker's simplicity in explaining the topic and would recommend any QA experts to join. At the webinar, I found it eye-opening when the speaker explained that we should avoid not related GxP SOPs, and I will share the information I learned with the management and try to improve existing SOPs. In any case, I think that such webinars are an excellent opportunity to reflect on essential topics in this field and receive a different point of view."

"I attended Qualistery's training on SOPs to get some useful pointers on improving writing and reducing deviation related to not sufficiently understanding an SOP. The webinar was fascinating, and I learned many valuable techniques to improve SOPs, such as reducing pages, adding visuals, and involving operators in manufacturing sop writing! I found it tremendously helpful that the presenter put in perspective the implications of inadequate SOPs with examples of companies who lost their license. I loved the webinar and found Qualistery's presentation style very useful, and I recommend it for QA, SME, and operators."

"I wanted to improve my knowledge of knowledge on SOP writing and decided to join Qualistery’s webinar on the topic. I loved how the presenter was clear and informative and brought excellent examples. If you are involved in writing and reviewing SOPs in any department, don't miss this webinar, as this training really gives you another perspective on effective SOP writing!"

“I joined Qualistery's webinar to get in touch with industry experts and the scientific community. I gained fresh insight and techniques for implementing continuous improvement within SOPs. I learned about the importance of implementing improvements to reduce deviations, costs and increase resource availability via right-first-time. After gaining new perspectives at the webinar, I will involve senior management in planned changes to gain support from Site Master Experts so different departments can work together as a team. Teamwork makes the dream work. Mostly, I loved listening to the industry expert bringing real-life scenarios and explaining how to overcome obstacles. This course is a must for anyone in the scientific community who wishes to stay up to date with current regulatory expectations. You will learn from real case studies to apply the knowledge learned in your working environment.”

"I really admired Qualistery's presentation as it is sincerely well done! The Q&A session was also very beneficial. I took the SOPs webinar, and it managed to change my mindset about the topic. Starting now, I will focus more on asking efficient questions to write a simple SOP that succeeds in meeting its aims rather than meeting an unreasonable deadline. The training itself is based on the communication between two generations in the pharmaceutical industry: the trainers, who are mostly people with high qualifications and a long experience in the field, and from the other side professionals who face everyday challenges in GxP compliance. During the event, you benefit from the interaction of both sides, and you enjoy an educational presentation. I think that Qualistery's training is excellent for all quality consultants within the pharmaceutical industry."

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.

€ 55 Excl. VAT

Live session
Q&A

€ 85 Excl. VAT

Live session
Q&A
Certificate of attendance
Presentation copy (post event)

Popular

€ 125 Excl. VAT

Live session
Q&A
Certificates of attendance
Presentation copy (post event)
Recording (30 days unlmited viewing)

* Prices are per delegate

FAQ

Most frequent questions and answers

Will I be able to communicate with the trainer?

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.

what software do you use for the training?

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

when will I get the acess link?

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.

I didn't get my access link! What do I do?

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!

I have encountered difficulties on the day of the webinar. What do I do?

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.

Should I use my webcam and microphone?

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.