U.S. health inspectors are still struggling to address a massive backlog of pharmaceutical plants that went uninspected during disruptions caused by COVID-19. That's according to an analysis of government data by the Associated Press. Read the full story here: https://buff.ly/47hkCeo
The Associated Press’ Post
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Understanding air classification in clean rooms is vital for maintaining a controlled environment in regulated sectors. Our expertise in monitoring particle counts sets us apart as the go-to partner for pharmaceutical and life sciences companies. Let us help you achieve optimal air quality standards. #ControlledEnvironment #ExpertSolutions #RegulationCompliance
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🌟 Curious about Product Master Data in the pharmaceutical industry? Dive into the latest insights and discover its vital importance in ensuring regulatory compliance and operational efficiency. 💯🤔 🚀 Explore the impact of Product Master Data on quality control, supply chain management, and decision-making processes. 🔗 Check out this insightful article from #Pharmuni for a deep dive into Product Master Data usage and benefits in the pharmaceutical landscape: https://lnkd.in/gYwCU5Uk 📝🔬 🙌 Join the conversation with the #Pharmatalks community and stay ahead of industry trends. Let's empower ourselves with knowledge and drive excellence in pharmaceutical data management together! 💪🌐🔒 #PharmaceuticalIndustry #DataQuality #RegulatoryCompliance #OperationalExcellence #Innovation #PatientSafety 🏥💻📈🔒
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Visionary of modern logistics, known for his transformational contributions and visions for the future
Severe storms threaten pharmaceutical production and storage and jeopardise the integrity of medicines. The industry is investing in robust infrastructures and comprehensive strategies to protect against climate-related disruptions and ensure a continuous supply of medicines. Read the Article today: Pharmaceutical industry prepares for climate disasters in the supply chainhttps://lnkd.in/djp7_ntQ
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To create a drug, technological innovation and human input work in synergy. Artificial intelligence can be a valuable tool, but when it comes to crucial processes like weighing active ingredients, human experience makes the difference. We talked about this, and many other topics, with Simone Franchi, Health, Safety and Environment Specialist, and Mariano Canale, Production Operator. 🔹 And you? What do you think about artificial intelligence in the pharmaceutical industry? Share your opinion. #IBSA #CaringInnovation #WeAreIBSA #IBSAVoices
#IBSAVoices - Double Interview
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Severe storms threaten pharmaceutical production and storage and jeopardise the integrity of medicines. The industry is investing in robust infrastructures and comprehensive strategies to protect against climate-related disruptions and ensure a continuous supply of medicines. Read the Article today: Pharmaceutical industry prepares for climate disasters in the supply chainhttps://lnkd.in/dbZHUzWp
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#Forced #degradation #studies play a crucial role in ensuring the safety, efficacy, and quality of pharmaceutical products. These studies involve subjecting drug substances and products to a variety of stress conditions, such as exposure to heat, light, humidity, and acidic or alkaline environments. By intentionally inducing degradation of the drug molecules, scientists can identify potential impurities or degradation products that may form under different storage conditions. This helps to assess the stability of the drug and determine the appropriate storage conditions to ensure its shelf-life. https://lnkd.in/ghraYDxp
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It is well recognized that poor quality can lead to supply disruption, a negative impact to business performance, and challenges for patients who rely on drugs and medicines. To drive positive change, the #drugmanufacturing sector should seek to greater enhance quality maturity, writes Samantha Atkinson of NSF in this new Outsourced Pharma article. https://lnkd.in/diprQrtH #qualitymanagement #pharma #biotech
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🔍 ALERT: Dr. Reddy’s Laboratories faces a staggering Rs 74.22 crore GST notice, revealing deep-rooted complexities in pharmaceutical GST compliance. This stark development signals potential pitfalls for companies navigating the intricate regulatory landscape. Want to explore the far-reaching implications for businesses and the industry? Read our latest article to know more https://ow.ly/Sy5450QXnl0 #GSTCompliance #PharmaIndustry #TaxLitigationManagement
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The pharmaceutical industry plays a vital role in global healthcare, bringing essential medicines and treatments to people in need worldwide. The realm of pharma freight forwarding requires meticulous planning, strict adherence to regulations, and careful handling to ensure the safe and efficient transportation of life-saving medicines and treatments. Independent freight forwarders specializing in pharmaceutical shipping face unique challenges and responsibilities in this crucial industry. Learn more ➡️ https://ow.ly/MvSz50RZOPy 🗣 Contact our team today to find out how we can support your Cold Chain needs... 📧 info@coldchainpacking.com 📲 +966 560 677 333 #ColdChain #SupplyChain #Pharma #Logistics #FreightForwarding
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𝐈𝐂𝐇 𝐐𝟏𝐀 (𝐑𝟐) 𝐆𝐮𝐢𝐝𝐞𝐥𝐢𝐧𝐞 🔬 👉 𝗪𝗵𝗮𝘁 𝗶𝘀 𝗜𝗖𝗛 𝗤𝟭𝗔 (𝗥𝟮)? ICH Q1A (R2) provides a comprehensive framework for assessing the stability of new drug substances and products. Understanding the intricacies of stability testing is pivotal to ensuring the efficacy, safety, and quality of pharmaceuticals over their shelf life. 📊💡 🌡️ 𝗪𝗵𝘆 𝗦𝘁𝗮𝗯𝗶𝗹𝗶𝘁𝘆 𝗧𝗲𝘀𝘁𝗶𝗻𝗴 𝗠𝗮𝘁𝘁𝗲𝗿𝘀: Stability testing evaluates how a drug's quality changes over time under various conditions. Factors such as temperature, humidity, and light can impact the stability of pharmaceuticals. Compliance with ICH Q1A (R2) ensures that products remain safe and effective from production to patient use. 🌿💉 🌐 𝗚𝗹𝗼𝗯𝗮𝗹 𝗖𝗼𝗹𝗹𝗮𝗯𝗼𝗿𝗮𝘁𝗶𝗼𝗻 𝗳𝗼𝗿 𝗤𝘂𝗮𝗹𝗶𝘁𝘆 𝗔𝘀𝘀𝘂𝗿𝗮𝗻𝗰𝗲: ICH Q1A (R2) is a result of collaboration between regulatory authorities and the pharmaceutical industry on a global scale. By adhering to these guidelines, companies contribute to the establishment of consistent standards that benefit patients worldwide. 🌍🤝 🚀 𝗖𝗼𝗻𝘁𝗶𝗻𝘂𝗼𝘂𝘀 𝗜𝗺𝗽𝗿𝗼𝘃𝗲𝗺𝗲𝗻𝘁 𝗮𝗻𝗱 𝗜𝗻𝗻𝗼𝘃𝗮𝘁𝗶𝗼𝗻: Stability testing is not only about compliance but also serves as a foundation for continuous improvement and innovation in drug development. Embracing these guidelines fosters a culture of excellence and ensures that the latest scientific advancements are integrated into pharmaceutical practices. 🚀🧪 Visit our website for more information. 📑 BIOBOSTON CONSULTING ➡ https://lnkd.in/gRD_hu4f #ichq1a #regulatoryaffairs #pharmaceuticalindustry #fdaapproval #biotechnology #medicaldevices #consulting
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