Join us at the 2024 PDA - Parenteral Drug Association Pharmaceutical Microbiology Conference next month! Our team will be on site discussing Ecolab Life Sciences contamination control solutions that help #pharmaceutical manufacturers reduce risk and meet regulatory requirements while driving quality. Learn more: 🔗 https://bit.ly/3VguTSn
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In pharmaceutical manufacturing, controlling contamination is critical to ensuring product safety and efficacy. The table below highlights common sources of potential contaminants 👇 A stringent contamination control strategy is essential to minimize these contaminants entering critical areas, and maintain the quality of pharmaceutical products! Learn how Dycem mats can help improve your contamination control strategy, reducing the risk of floor-level contamination ➡️ https://lnkd.in/edut7AB7. #pharmaindustry #contaminationcontrol #reducerisk #pharmaceuticals #pharmaceuticalmanufacturing #cleanrooms #cleanroomtechnology
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Are you adequately testing #pharmaceuticals for API stability, consistent dosing, and bioavailability? Ensure regulatory compliance and accelerate time to market by making rheology the foundation of your lab. Get to the core of your pharmaceutical performance with rheology. Stay tuned for a new rheology solution to streamline pharmaceutical development. #Pharma #Pharmaceuticals #PharmaIndustry #DrugDiscovery
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🧬 R&D and Innovation Director 🇫🇷 🇧🇪 🔬 Analytical Sciences 🦠 Innovative Therapies 🧫
📢 The recent announcement from US Pharmacopeia allowing the use of non-animal-derived reagents for endotoxin testing is a significant milestone for the pharmaceutical industry (https://lnkd.in/emRNwfXa). This change not only promotes ethical practices by reducing reliance on animal-derived products 🐰 but also enhances the consistency and reliability of testing outcomes 🔍. At QUALITY ASSISTANCE S.A., we are proud to be at the forefront of this advancement. Our state-of-the-art analytical services already include endotoxin testing using recombinant reagents 🧬, ensuring high precision and adherence to the latest industry standards. 📄 We invite you to explore our detailed application note on this topic, where we delve into the benefits and technical aspects of using alternative analytical solutions for endotoxin analysis. 🔗 Full application note available here: https://lnkd.in/eZZspM-P The brochure detailing the analytical services we offer for endotoxin testing is available here: https://lnkd.in/eGkAQW8V Together, let's drive innovation and quality in pharmaceutical testing 🚀. #PharmaceuticalTesting #QualityAssurance #EndotoxinTesting #Innovation #Sustainability
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Great article letting you know how Infinity Laboratories can help with ensuring that the methods and materials you use in cleaning your cleanrooms are as effective as required.
Complying with USP Disinfectant Efficacy Guidelines in Pharmaceutical Manufacturing Environments Pharmaceutical manufacturers must demonstrate that the disinfectants and antiseptics they use in their manufacturing facilities effectively control contaminants to ensure patient safety and compliance with regulatory requirements. The best way to ensure that cleanrooms are cleaned consistently, disinfected effectively, and that common pathogens are eliminated, is to study the efficacy of the disinfectants used in a manufacturer’s regular cleaning processes. Click below to read the full article: https://lnkd.in/eKiqdnC9
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Director I Scientist I AI technologist @ Gplife → 19 Years of expertised- Pharmaceutical technology in Longevity I Anti-aging I Cell regeneration I Cosmeceuticals I Chronic disease reversal Phyto industry
📢 Attention pharmaceutical industry professionals! The World Health Organization (WHO) has released new guidelines for excipients used in pharmaceutical products. These guidelines include an appendix listing examples of high-risk excipients that are restricted due to their potential to cause cancer and other severe diseases. We are proud to say that our patented technology has allowed us to produce excipientless dosage forms since 2006, in line with these latest guidelines. Stay informed and ensure the safety of your pharmaceutical products by following the WHO's guidelines for excipients. Let's work together to prioritize the health and well-being of patients around the world. #pharmaceuticals #WHOguidelines #excipientsafety #patienthealth
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Director of Quality Assurance, Warehouses and Regulatory Affairs - PHYTOPHARMA (23 year experience working in Pharma industry in Quality Assurance, Warehouses, Regulatory Affairs, Supply Chain plus Medical, Marketing)
Let’s check our knowledge on pharmaceutical industry, esp. Pharmacists and those who are working in pharma supply chain: 1. What are the two missions of pharma industry ? 2. Which regulations/ guidelines are being used in pharmaceutical quality management ? Fyi, less than 10% people working in pharma industry give the right answer to the (1) 😄😄😄
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Global Exporter of Pharmaceuticals, APIs, Agrochemicals, and Industrial Chemicals | Quality-Driven Since 2017
Aceclofenac API Aceclofenac is a non-steroidal anti-inflammatory drug (NSAID) commonly used to relieve pain and inflammation in conditions such as arthritis. As an API (Active Pharmaceutical Ingredient), aceclofenac is utilized in the manufacturing of various pharmaceutical formulations, including tablets, capsules, and topical gels. For inquiries about Aceclofenac API or our full range of pharmaceutical APIs, please contact us today. We are here to provide tailored solutions to meet your requirements. #Pharmaceuticals #API #Aceclofenac #NSAIDs #PharmaIndustry #Healthcare #DrugManufacturing #PharmaSolutions #ActivePharmaceuticalIngredient #PharmaSupplyChain
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