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Course overview
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.

 

Speaker:

Antiksha Joshi
QMS and GMP Trainer/Facilitator

 

Available Dates

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