In the rapidly evolving world of healthcare product development and manufacturing, the post-pandemic era has brought about unprecedented challenges and opportunities. To thrive in this new environment, companies must adapt swiftly to ever-changing requirements while maintaining unwavering product quality and patient safety. Embracing holistic approaches to manage business operations effectively is crucial for success.
We are excited to present a comprehensive 4-part virtual training series, designed to help you navigate this new era of healthcare product development and manufacturing. This series will focus on QMS principles, data integrity, document management, and creating effective SOPs to support your organisation in improving efficiency, achieve sustainable compliance, and build customer trust.
This training is for professionals working within the pharmaceutical, life science, clinical trials, and medical device sector. These sessions are applicable to those working in GMP, Regulatory Affairs, Medical Devices, Pharmacovigilance, Medical Operations, Clinical Research or Quality.
To see the individual sessions in this four-part series course, please use the links below
Quality Management Systems – General Principles and Implementation
29 April - 10:30-12:00 (AEST)
Building strong foundations for Digital transformation: Good Documentation and Data integrity practices
17 May 10:30-12:00 (AEST)
Document Management and Control
7 June - 10:30-12:00 (AEST)
Writing effective and compliant SOPs and work instructions
28 June - 10:30-12:00 (AEST)
1.Gain a deep understanding of QMS principles and how they support efficiency and sustainable compliance in the post-pandemic era.
2.Discover the importance of data integrity in the success of digital projects and learn how to ensure its application throughout your organisation.
3.Explore the role of documents in compliance and building customer trust, and master best practices for document management and control.
4.Learn the art of creating SOPs that are effective, compliant, and adaptable to the ever-changing business landscape.
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.
Course fees (inc. GST)
Early bird - until 1 Apr
ARCS member - $385
Non-member - $580
Standard - from 2Apr
ARCS member - $480
Non-member - $720
.png){kind=logo}
.png)
%20(2).jpg)
