Uncover the strategies behind Gedeon Richter’s success in implementing a digital quality management system. Join our webinar to learn from industry leaders and kickstart your own journey towards quality management excellence. Reserve your spot now!
Join us to explore the new EUDAMED Regulations and understand why companies have been silent about their concerns. We will examine the key provisions, implications, and challenges faced by companies in complying with these regulations. Discover the potential barriers hindering their complaints and gain comprehensive insights into the impact on the medical device industry.
Stay ahead in the ever-evolving world of Medical Device and Pharmaceutical Regulations. Join us for the Important Regulatory Highlights for Pharma and Medtech for 2023/24 webinar. Gain insights from our expert presenter, Martin King, with over 40 years of global experience in the industry. Understand the changes impacting the regulatory landscape and discover what to expect in 2024. Don’t miss this opportunity to stay informed and succeed in your daily business operations. Register now!
Join our exclusive webinar and learn how to navigate regulatory authority inspections. Led by industry expert Charley Maxwell, this one-hour session will provide valuable insights into responding to non-conformances cited during inspections. Gain a clear understanding of expectations, timelines, and effective root cause analysis. Designed for senior management, quality professionals, and compliance heads, this webinar will equip you with the knowledge to address regulatory challenges and prioritize patient safety. Don’t miss this opportunity to ensure a successful outcome following inspections. Register now to secure your spot!
Learn the tips and tricks for using the eQMS system to capture project knowledge and streamline the workflow of regulatory submissions, especially when multiple subcontractors and consultants are involved.
To understand regulators’ expectations concerning interpreting the new USP Chapter <1083>. Also, gain an overview of the EU guidelines about supplier qualification, highlighting differences between the standards where applicable.
To understand regulators’ expectations concerning interpreting the new USP Chapter <1083>. Also, gain an overview of the EU guidelines about supplier qualification, highlighting differences between the standards where applicable.
Join us to gain in depth overview of the regulatory and good practice requirements around partnering with contract manufacturing, testing, storage, and distribution organizations. You will learn the expectations from the regulators and when and to what extent to engage with each type of contractor.
Sign up for our comprehensive online on-demand GMP refresher course today and take control of your knowledge and skills in the field.
By joining this webinar you will get an insight into the requirements for commercialisation and licencing to launch established products in the EU.
Download our free Ultimate FMEA Guide, which is dedicated to GMP and pharma professionals.
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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