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.
Stay updated on latest GMP trends through our webinars and articles
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!
Choosing the Right Solution: 8 Factors to Consider for Successful Automation in Temperature Monitoring
Dive deep into the article below and explore the 8 crucial factors that should be taken into account when choosing automated temperature monitoring equipment.
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!
Join our webinar on the latest cold storage technology for the pharmaceutical industry. Discover how forced-air convection can revolutionize your operations, optimize workflow, and protect sample integrity. Register now to stay ahead in pharmaceutical manufacturing.