Our production facilities are FDA-inspected and manufacture under IPEC Guidelines for cGMP compliance, enabling us to supply lactose that conforms to all globally recognised compendial monographs. We have also developed and implemented stringent quality control systems to provide complete traceability for all our products and optimal batch-to-batch consistency. We are fully committed to delivering high-quality lactose that meets and exceeds your expectations. Reach out to our experts to explore top quality lactose for your needs: https://lnkd.in/eDc_248x #KerryPharma #PharmaLactose #Lactose
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Sterility is critical in #pharmaceuticals, requiring #hygienic instruments with strict #isolation, #sterilization, and no contamination risks. LEEG's sanitary pressure transmitters like SMP858-NSF are designed to meet the highest #food and #drug production standards, with features like full isolation and high overload protection. Unlock how the #LEEG #transmitter can help with Ganoderma lucidum extraction. https://lnkd.in/gn72wqYT
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Electrolab Dissolution Apparatus 👩🏻🔬🧪 It is an apparatus approved by USFDA (United States Food and Drug Administration) and considered as one of the major IPQC i.e In-Process Quality Control Test for testing of various API or finished products to check its in vitro release rate in acidic basic or in any pH dissolution media. The release of the drug occurs according to its release pattern w.r.t different dosage forms like:- a. Conventional release dosage form :- 1 hour Max b. Sustained release dosage form :- 4-8 hours Max c. Extended release dosage form :- 10-24 hours Max . . #pharmaceutical_research #pharma_world #dissolution #laboratory_test
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A great milestone with our peptide portfolio.. 👍 The Tirzepetide molecule is available and nGMP samples can be shared to support your strategy. The team and myself are here to answer your questions and provide support till the successful submission and launch. Talk to me #peptide #Tirzepetide #tevaapi
We're here to support your global Tirzepatide strategy! With deep peptide API development and manufacturing experience, a large portfolio of generic commercial peptides, and 24 DMFs for 8 peptides already under our belt, we'd be delighted to talk to you today. nGMP samples are available. For more information visit: https://lnkd.in/eEJs5SVW 𝘛𝘪𝘳𝘻𝘦𝘱𝘢𝘵𝘪𝘥𝘦 𝘈𝘗𝘐 𝘪𝘴 𝘤𝘶𝘳𝘳𝘦𝘯𝘵𝘭𝘺 𝘥𝘦𝘷𝘦𝘭𝘰𝘱𝘦𝘥 𝘢𝘯𝘥 𝘱𝘳𝘰𝘥𝘶𝘤𝘦𝘥 𝘧𝘰𝘳 𝘙&𝘋 𝘱𝘶𝘳𝘱𝘰𝘴𝘦𝘴 𝘢𝘯𝘥 𝘳𝘦𝘨𝘶𝘭𝘢𝘵𝘰𝘳𝘺 𝘴𝘶𝘣𝘮𝘪𝘴𝘴𝘪𝘰𝘯𝘴 𝘰𝘯𝘭𝘺. 𝘛𝘩𝘦 𝘴𝘢𝘭𝘦 𝘪𝘴 𝘦𝘹𝘤𝘭𝘶𝘥𝘦𝘥 𝘦𝘹𝘤𝘦𝘱𝘵 𝘧𝘰𝘳 𝘵𝘩𝘦 𝘱𝘶𝘳𝘱𝘰𝘴𝘦𝘴 𝘰𝘧 𝘰𝘣𝘵𝘢𝘪𝘯𝘪𝘯𝘨 𝘰𝘯𝘦 𝘰𝘳 𝘮𝘰𝘳𝘦 𝘮𝘢𝘳𝘬𝘦𝘵𝘪𝘯𝘨 𝘢𝘶𝘵𝘩𝘰𝘳𝘪𝘻𝘢𝘵𝘪𝘰𝘯𝘴 𝘢𝘯𝘥 𝘰𝘯𝘭𝘺 𝘪𝘧 𝘵𝘩𝘦 𝘭𝘢𝘵𝘵𝘦𝘳 𝘴𝘢𝘭𝘦 𝘪𝘴 𝘱𝘦𝘳𝘮𝘪𝘴𝘴𝘪𝘣𝘭𝘦 𝘶𝘯𝘥𝘦𝘳 𝘢𝘯𝘥 𝘪𝘯 𝘢𝘤𝘤𝘰𝘳𝘥𝘢𝘯𝘤𝘦 𝘸𝘪𝘵𝘩 𝘢𝘱𝘱𝘭𝘪𝘤𝘢𝘣𝘭𝘦 𝘭𝘢𝘸. #tirzepatide #glp1 #activepharmaceuticalingredients #tevaapi
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Pharmaceutical freeze dryers, installed in Class D areas, integrate a product door (pizza door) on a pharma wall, directly to Class A for operation with sterile drugs in opened containers (half-stoppered vials). Once closed, the tight vacuum vessels maintain a level below 0.01mbar l/s, protecting the product. Sterilization between batches is necessary to deactivate microbial contamination, achieved through steam or VHP methods. Steam sterilization, at 121ºC and 2 bar(a), is reliable and homogeneous, while VHP sterilization relies on hydrogen peroxide's oxidative properties. Freeze dryers designed for steam sterilization follow vessel regulations, though they incur higher costs, they offer reliability and ease of validation. Lyoptimus Thermodynamics Learn more: https://lnkd.in/efcWyjk5 #Speakpharma #LyoptimusThermodynamics #Annex1 #Lyophilization #AsepticProcessing #Compliance #GMP #GAMP5 #PharmaRegulation #SterileManufacturing #EMA #FDA #PICs #WHO #Pharmaceuticals #DrugManufacturing #QualityControl #RegulatoryCompliance #DrugSafety #PharmaTech #PharmaIndustry #ManufacturingStandards #RegulatoryGuidelines
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🌟 𝐃𝐢𝐬𝐜𝐨𝐯𝐞𝐫 𝐭𝐡𝐞 𝐩𝐨𝐰𝐞𝐫 𝐨𝐟 𝐀𝐫𝐠𝐢𝐧𝐢𝐧𝐞 𝐇𝐂𝐋 𝐈𝐧𝐣𝐞𝐜𝐭𝐢𝐨𝐧 𝐆𝐫𝐚𝐝𝐞 💉, your reliable choice for pharmaceutical excellence. Our product stands out with a robust combination of 📄 DMF & GMP certifications, ensuring the highest standards of safety and quality are met. 💰 But that's not all—enjoy the peace of mind that comes with a very competitive price, making us a smart choice for your business's growth. 📚 Furthermore, we provide full document support to facilitate a smooth API registration process, saving you time and resources. 🏆 Stay ahead in the healthcare industry by choosing Arginine HCL Injection Grade—where quality, affordability, and compliance come together seamlessly. 🔍 Follow us on LinkedIn and Facebook for more insights into our products and the latest industry trends. 🌐 www.sncnutra.com 📧 sales@globalsnc.com #PharmaceuticalExcellence #CompetitiveEdgeInHealthcare
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We're here to support your global Tirzepatide strategy! With deep peptide API development and manufacturing experience, a large portfolio of generic commercial peptides, and 24 DMFs for 8 peptides already under our belt, we'd be delighted to talk to you today. nGMP samples are available. For more information visit: https://lnkd.in/ez-CEuic 𝘛𝘪𝘳𝘻𝘦𝘱𝘢𝘵𝘪𝘥𝘦 𝘈𝘗𝘐 𝘪𝘴 𝘤𝘶𝘳𝘳𝘦𝘯𝘵𝘭𝘺 𝘥𝘦𝘷𝘦𝘭𝘰𝘱𝘦𝘥 𝘢𝘯𝘥 𝘱𝘳𝘰𝘥𝘶𝘤𝘦𝘥 𝘧𝘰𝘳 𝘙&𝘋 𝘱𝘶𝘳𝘱𝘰𝘴𝘦𝘴 𝘢𝘯𝘥 𝘳𝘦𝘨𝘶𝘭𝘢𝘵𝘰𝘳𝘺 𝘴𝘶𝘣𝘮𝘪𝘴𝘴𝘪𝘰𝘯𝘴 𝘰𝘯𝘭𝘺. 𝘛𝘩𝘦 𝘴𝘢𝘭𝘦 𝘪𝘴 𝘦𝘹𝘤𝘭𝘶𝘥𝘦𝘥 𝘦𝘹𝘤𝘦𝘱𝘵 𝘧𝘰𝘳 𝘵𝘩𝘦 𝘱𝘶𝘳𝘱𝘰𝘴𝘦𝘴 𝘰𝘧 𝘰𝘣𝘵𝘢𝘪𝘯𝘪𝘯𝘨 𝘰𝘯𝘦 𝘰𝘳 𝘮𝘰𝘳𝘦 𝘮𝘢𝘳𝘬𝘦𝘵𝘪𝘯𝘨 𝘢𝘶𝘵𝘩𝘰𝘳𝘪𝘻𝘢𝘵𝘪𝘰𝘯𝘴 𝘢𝘯𝘥 𝘰𝘯𝘭𝘺 𝘪𝘧 𝘵𝘩𝘦 𝘭𝘢𝘵𝘵𝘦𝘳 𝘴𝘢𝘭𝘦 𝘪𝘴 𝘱𝘦𝘳𝘮𝘪𝘴𝘴𝘪𝘣𝘭𝘦 𝘶𝘯𝘥𝘦𝘳 𝘢𝘯𝘥 𝘪𝘯 𝘢𝘤𝘤𝘰𝘳𝘥𝘢𝘯𝘤𝘦 𝘸𝘪𝘵𝘩 𝘢𝘱𝘱𝘭𝘪𝘤𝘢𝘣𝘭𝘦 𝘭𝘢𝘸. #tirzepatide #glp1 #activepharmaceuticalingredients #tevaapi
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Full control and deep understanding of the process bring you the product with no surprises by the team of professionals you can trust.
We're here to support your global Tirzepatide strategy! With deep peptide API development and manufacturing experience, a large portfolio of generic commercial peptides, and 24 DMFs for 8 peptides already under our belt, we'd be delighted to talk to you today. nGMP samples are available. For more information visit: https://lnkd.in/eEJs5SVW 𝘛𝘪𝘳𝘻𝘦𝘱𝘢𝘵𝘪𝘥𝘦 𝘈𝘗𝘐 𝘪𝘴 𝘤𝘶𝘳𝘳𝘦𝘯𝘵𝘭𝘺 𝘥𝘦𝘷𝘦𝘭𝘰𝘱𝘦𝘥 𝘢𝘯𝘥 𝘱𝘳𝘰𝘥𝘶𝘤𝘦𝘥 𝘧𝘰𝘳 𝘙&𝘋 𝘱𝘶𝘳𝘱𝘰𝘴𝘦𝘴 𝘢𝘯𝘥 𝘳𝘦𝘨𝘶𝘭𝘢𝘵𝘰𝘳𝘺 𝘴𝘶𝘣𝘮𝘪𝘴𝘴𝘪𝘰𝘯𝘴 𝘰𝘯𝘭𝘺. 𝘛𝘩𝘦 𝘴𝘢𝘭𝘦 𝘪𝘴 𝘦𝘹𝘤𝘭𝘶𝘥𝘦𝘥 𝘦𝘹𝘤𝘦𝘱𝘵 𝘧𝘰𝘳 𝘵𝘩𝘦 𝘱𝘶𝘳𝘱𝘰𝘴𝘦𝘴 𝘰𝘧 𝘰𝘣𝘵𝘢𝘪𝘯𝘪𝘯𝘨 𝘰𝘯𝘦 𝘰𝘳 𝘮𝘰𝘳𝘦 𝘮𝘢𝘳𝘬𝘦𝘵𝘪𝘯𝘨 𝘢𝘶𝘵𝘩𝘰𝘳𝘪𝘻𝘢𝘵𝘪𝘰𝘯𝘴 𝘢𝘯𝘥 𝘰𝘯𝘭𝘺 𝘪𝘧 𝘵𝘩𝘦 𝘭𝘢𝘵𝘵𝘦𝘳 𝘴𝘢𝘭𝘦 𝘪𝘴 𝘱𝘦𝘳𝘮𝘪𝘴𝘴𝘪𝘣𝘭𝘦 𝘶𝘯𝘥𝘦𝘳 𝘢𝘯𝘥 𝘪𝘯 𝘢𝘤𝘤𝘰𝘳𝘥𝘢𝘯𝘤𝘦 𝘸𝘪𝘵𝘩 𝘢𝘱𝘱𝘭𝘪𝘤𝘢𝘣𝘭𝘦 𝘭𝘢𝘸. #tirzepatide #glp1 #activepharmaceuticalingredients #tevaapi
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In October 2024, the FDA released an updated guidance on the bioequivalence of immediate-release solid oral dosage forms. This new guideline outlines essential standards and methodologies for establishing bioequivalence, helping ensure that medicinal products meet the necessary quality, efficacy, and safety standards. Check out the full guidance below for all the details and insights. #Bioequivalency #GMP #Quality #OralSolisDosageForm
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Antibiotice, 𝘄𝗼𝗿𝗹𝗱𝘄𝗶𝗱𝗲 𝗹𝗲𝗮𝗱𝗶𝗻𝗴 𝗺𝗮𝗻𝘂𝗳𝗮𝗰𝘁𝘂𝗿𝗲𝗿 𝗼𝗳 𝗡𝘆𝘀𝘁𝗮𝘁𝗶𝗻 𝗔𝗣𝗜𝘀. For Nystatin (active substance) we have obtained the following certifications over time: 🔸 EU GMP 🔸 US FDA 🔸 Certification of Suitability According to European Pharmacopoeia 🔸 numerous approvals from clients and audit specialized companies (Rephine, SGS, Blue Inspection Body) from different parts of the world Since 2017, 𝗡𝘆𝘀𝘁𝗮𝘁𝗶𝗻 𝗔𝗻𝘁𝗶𝗯𝗶𝗼𝘁𝗶𝗰𝗲 has become the US Pharmacopoeia reference standard. Currently, the Nystatin produced by Antibiotice is sold in more than 60 countries worldwide. Let’s talk about it @ CPHI 𝗠𝗶𝗹𝗮𝗻, on 8-10 October. #TheFutureTogether #CPHI #pharmaindustry #CPHIMilan
Nystatin Antibiotice
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Is your company involved in manufacturing active pharmaceutical ingredients (APIs) and aware of the specific packaging requirements? Challenge CurTec to find the perfect solution for you. CurTec offers drums, pails, and jars designed for API bulk packaging with the following benefits: - Moisture Vapor Tight Closure: Our plastic bulk packaging features a rubber gasket in the lids to prevent the hardening or caking of powders. - Food Safe: Our packaging materials are free from harmful chemicals or contaminants that could affect the contents. - Sealability: All our bulk packaging is sealable, enhancing safety and visibility. Our tamper-evident features help prevent or reveal any unauthorized access. - Optically Clean: Our packaging maintains a high level of cleanliness to avoid contamination of valuable APIs. https://www.curtec.com/en
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