Enhance your supplier management practices by joining our webinar on “How to Effectively Prepare for a Supplier Qualification Audit.” Discover proven strategies to streamline the audit process and optimize supply chain efficiency. Register now to elevate your skills in supplier qualification audits and unlock the key to successful supplier relationships.
Uncover the crucial role of freeze/thaw processes in pharmaceutical operations. Gain insights into industry challenges, explore innovative solutions, and revolutionize your approach to drug substance preservation for enhanced manufacturing success. Reserve your spot now to stay ahead in pharmaceutical advancements and drive efficiency in your operations!
Join us for an insightful webinar that delves into the advanced aspects of ICH Q9, offering real-life examples and practical advice to enhance your pharmaceutical risk management strategies.
Integration of Al in pharmaceutical manufacturing
Using artificial intelligence (AI) and machine learning (ML) are the most innovative technologies that are increased over the past few years in Pharmaceutical industry.
the integration of AI technologies holds great promise for accelerating drug development, improving patient outcomes, and revolutionizing the pharmaceutical industry
Learn how to streamline batch record workflows, enhance real-time data access, reduce costs, and ensure regulatory compliance. Discover practical strategies to empower your workforce with digital tools for greater efficiency and productivity.
The analysis identified 103 different genera, including bacteria, molds, and yeast, with the top two frequently isolated microorganisms being Pseudomonas spp and Bacillus spp. Pseudomonas spp, gram-negative rods, are common in water sources and manufacturing settings, posing contamination risks in various industries. Bacillus spp, gram-positive rods with endospores, are prevalent in finished products and raw materials, playing a vital role in industrial biotechnology. Understanding these microorganisms is crucial for effective quality control and prevention of microbial contamination.
Working at quality could be stressful, frequently fighting compliance issues or critical deviations
affecting production. Heroes rewarded for flowing to the work enabling restart of operations after an
unpredicted failure or unexpected warning letter from regulatory board. How can organization
culture move from heroic to strategic?
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.
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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