Learn how to apply the key elements of pharmaceutical risk management, implement the ICH Q9 risk model in your business, and access tools for natural risk management integration. Join us to elevate your product lifecycle with effective risk assessment and control strategies.
Join our exclusive webinar to uncover the secrets of effective investigations and root cause analysis. Enhance compliance and boost success in your company’s quality management systems.
The PIP scandal highlights the crucial need for stringent medical device regulation, exemplified by the Medical Device Regulation (2017/745). This crisis exposed the consequences of lax oversight in the industry.
This article explores six key regulatory updates in the European pharmaceutical and medical technology industries, highlighting the importance of staying informed and prepared for future changes.
Join us from January 16th to 18th for a special event designed for pharmaceutical and biotech companies focused on quality. Get expert guidance for achieving therapeutic quality excellence.
Our latest article delves into the nuances of FDA’s Form 483, offering essential guidance on how to transform FDA observations into concrete actions.
In this blog, we will delve deeper into the European regulations and guidelines that meticulously dictate the temperature storage requirements in the pharmaceutical domain. From understanding the basic principles to analyzing the nuanced details, we will provide you with a comprehensive guide to remain compliant throughout the entire lifecycle of temperature-sensitive products.
In an industry that is constantly evolving, it’s crucial to stay informed about the latest trends and updates. In this article, we shall journey into the heart of Good Manufacturing Practice (GMP) — reviewing the key changes and developments over recent years.
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!
Dive deep into the article below and explore the 8 crucial factors that should be taken into account when choosing automated temperature monitoring equipment.
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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