Writing Effective and Compliant SOPs and Work Instructions in the age of AI

Start Date
13 March 2026
End Date
13 March 2026
Start Time
11:30
End Time
14:00
Venue
ARCS Virtual Classroom
Who Can Register?
Anyone

New course!

Topic 3 – Writing Effective & Compliant SOPs and Work Instructions in the age of AI

 

Overview: Clear, concise, and unambiguous procedures and instructions are the foundations for compliance and efficient processes. They play a key role in minimizing human errors in a regulated industry. Hence, developing the skills to write such documents is important. Furthermore, understanding the components of effective SOPs and Work Instructions becomes increasingly crucial as organizations transition towards leveraging AI technologies in their operations.

 

This virtual session is designed as a workshop and is a blend of instructional section and brainstorming exercises. In this session we will learn the steps involved in identifying & drafting a good SOP as well as the common roadblocks that hinder effective use of SOPs.

 

Learning Objectives:

At the end of this session, attendees will:

  1. Identify the root causes of ineffective SOPs.
  2. Learn tools that help create effective SOPs.
  3. Be able to identify the key features of a well written SOP.
  4. Gain foundational knowledge on creating AI prompts for drafting good SOPs.
  5. Draft examples SOPs and Work Instructions.

Who Should attend:

This training is for professionals working within the pharmaceutical, life science, clinical trials, and medical device sector. It is particularly beneficial for individuals who are responsible for drafting and reviewing SOPs and Work Instructions. A prior basic knowledge of GMP document control will be useful, however, it is not mandatory.

 

Speaker:

Antiksha Joshi is an accomplished quality systems professional with over 20 years of experience in the pharmaceutical and life science industry. Throughout her career, she has demonstrated a strong commitment to ensuring compliance, efficiency, and excellence in quality management systems (QMS). With a passion for improving organizational processes, Antiksha has played a pivotal role in implementing and enhancing QMS at various organizations. Her expertise has been instrumental in leading successful regulatory audits and inspections, contributing to the overall success and reputation of the companies she has worked with. As the founder and leader of her consulting firm, Urmi Quality Management Consulting Pty Ltd, she is dedicated to supporting pharmaceutical and life science companies in achieving compliant, robust, and user-friendly quality systems. She also actively gives back to the community as a volunteer mentor for STEM students, inspiring and guiding the next generation of aspiring professionals in science, technology, engineering, and mathematics.  

Registration fees:

 


ARCS member - $180+ GST
Non-member - $255 +GST