Solvias

Solvias

Arzneimittelherstellung

Kaiseraugst, AG 13.586 Follower:innen

Solvias is a world leader in pharmaceutical CMC analysis (CRO).

Info

Solvias ist Weltmarktführer im Bereich Auftragsforschung, Entwicklung und Herstellung (CRO/CDMO). Wir sind hauptsächlich für die Pharma-, Biotech-, Medizintechnik- und die Kosmetikindustrie tätig. Unsere Laboratorien arbeiten nach den höchsten Standards und entsprechend den Richtlinien von ISO, cGMP und GLP (Hombourg). Mit unserer hervorragenden Infrastruktur und beispiellosen Expertise entwickeln, analysieren und prüfen wir eine grosse Vielzahl von biologischen und chemischen Substanzen und Produkten. Wir können uns dabei auf unsere breite und gut etablierte wissenschaftliche Erfahrung und unsere bisherigen Erfolge abstützen und bieten integrierte Dienstleistungen, Produkte und Technologien an, die die Wertschöpfungskette für unsere weltweiten Kunden verbessern.

Branche
Arzneimittelherstellung
Größe
501–1.000 Beschäftigte
Hauptsitz
Kaiseraugst, AG
Art
Privatunternehmen
Gegründet
1999
Spezialgebiete
Analytical Services, Solid State Development (Polymorphism, Salts and Crystallization), Pharmaceutical Development, Catalysis Technology, Biopharmaceutical Analysis, API Manufacturing, Biological Analysis, Custom Synthesis, Small Molecules Analysis, Ligands, Extractables & Leachables, Quality Control, Troubleshooting, Cell & Gene Therapy, mAbs & ADCs und Biologics

Orte

Beschäftigte von Solvias

Updates

  • Unternehmensseite von Solvias anzeigen, Grafik

    13.586 Follower:innen

    Our insightful session on advanced Extractables and Leachables (E&L) screening is now available on demand. Led by Ulli Hohenester, Team Leader for E&L and HRAM Trace Analysis at Solvias, this webinar explores the use of High-Resolution Mass Spectrometry (HRAM-MS) combined with liquid and gas chromatography (LC, GC). Discover how these techniques are transforming E&L analysis, enabling more precise identification at lower analytical thresholds. 🔗 Watch now: https://lnkd.in/e9WeiPpX #extractables #leachables #E&L #HRAM #webinar

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  • Unternehmensseite von Solvias anzeigen, Grafik

    13.586 Follower:innen

    Cell-based bioassays (CBBAs) are essential for the development of advanced therapies, but their complexity and variability require careful navigation. We now have two valuable resources to support your success: 📄 White Paper: "The Potency Puzzle: Overcoming Challenges in Potency Assays for Cell and Gene Therapy Development" https://lnkd.in/eif74Kir 🎥 Webinar Recording: "Navigating Complexity: Tailoring Cell Based Bioassays for Advanced Therapeutics" https://lnkd.in/eraRFxJv Access both resources now and learn how to overcome CBBAs challenges. #CBBA #cellbasedbioassays #bioassays #PotencyAssays #CellAndGeneTherapy #Biologics

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  • Unternehmensseite von Solvias anzeigen, Grafik

    13.586 Follower:innen

    It's important to have a lab that supports the entire life cycle of cell & gene therapy CMC analytical development. This allows for molecule and method specific knowledge to be easily transferred from characterization, through method development, validation, and ultimately GMP commercial release testing. #CGT #AAV #celltherapy #genetherapy #CMC #GMP #analyticaldevelopment

    Unternehmensseite von Solvias anzeigen, Grafik

    13.586 Follower:innen

    Biologics and cell & gene therapies are the fastest-growing areas in the pharmaceutical industry. These complex molecules are produced in living cells through multistep processes, making precise analytical methods essential for quality control and regulatory approval. A broad range of methods is required to ensure identity, purity, potency, safety, and immunochemical properties. Among these, three stand out for their high flexibility and versatility: Capillary Electrophoresis (CE), Enzyme-Linked Immunosorbent Assay (ELISA), and Surface Plasmon Resonance (SPR). ✔️ ELISA: A highly sensitive method for detecting and quantifying process-related impurities, such as host cell proteins (HCP), which is critical for ensuring product safety during release analysis. ELISA is the gold standard method for measuring protein affinity to its target, and is commonly used in potency assays for both release and stability testing. ✔️ CE: A high-resolution separation technique for the analysis of a wide variety of biomolecules, from amino acids to viral particles. Providing great separation efficiency, CE surpasses other conventional techniques such as LC in many aspects. CE methods available at Solvias include CGE (UV, LIF), CGE-SDS (UV, LIF), cIEF (UV, FL, MS), and CZE (UV, LIF, MS). These methods assess product quality by analyzing isoforms, impurities, as well as size and charge heterogeneity. ✔️ SPR: Our SPR services offers comprehensive, real-time, label-free analysis that preserves the natural state of molecules and provides immediate insights into binding interactions. These services include affinity measurement (KD), on- and off-rate determination (kon and koff), potency assessment (EC50), batch-to-batch comparability, and stability testing. ✉️ Reach out to us at info@solvias.com to discover how these methods can advance your biologics and cell & gene therapies development.

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  • Unternehmensseite von Solvias anzeigen, Grafik

    13.586 Follower:innen

    Biologics and cell & gene therapies are the fastest-growing areas in the pharmaceutical industry. These complex molecules are produced in living cells through multistep processes, making precise analytical methods essential for quality control and regulatory approval. A broad range of methods is required to ensure identity, purity, potency, safety, and immunochemical properties. Among these, three stand out for their high flexibility and versatility: Capillary Electrophoresis (CE), Enzyme-Linked Immunosorbent Assay (ELISA), and Surface Plasmon Resonance (SPR). ✔️ ELISA: A highly sensitive method for detecting and quantifying process-related impurities, such as host cell proteins (HCP), which is critical for ensuring product safety during release analysis. ELISA is the gold standard method for measuring protein affinity to its target, and is commonly used in potency assays for both release and stability testing. ✔️ CE: A high-resolution separation technique for the analysis of a wide variety of biomolecules, from amino acids to viral particles. Providing great separation efficiency, CE surpasses other conventional techniques such as LC in many aspects. CE methods available at Solvias include CGE (UV, LIF), CGE-SDS (UV, LIF), cIEF (UV, FL, MS), and CZE (UV, LIF, MS). These methods assess product quality by analyzing isoforms, impurities, as well as size and charge heterogeneity. ✔️ SPR: Our SPR services offers comprehensive, real-time, label-free analysis that preserves the natural state of molecules and provides immediate insights into binding interactions. These services include affinity measurement (KD), on- and off-rate determination (kon and koff), potency assessment (EC50), batch-to-batch comparability, and stability testing. ✉️ Reach out to us at info@solvias.com to discover how these methods can advance your biologics and cell & gene therapies development.

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  • Unternehmensseite von Solvias anzeigen, Grafik

    13.586 Follower:innen

    It’s 6:02 a.m., and we’re already posting on LinkedIn. Too early? Not today! That’s because today is Mole Day, celebrated on October 23 from 6:02 a.m. to 6:02 p.m., in honor of Avogadro's Number (6.02 x 10²³). One mole of a substance contains Avogadro's number of elementary entities. For example, 1 mole of copper contains 6.02214076 x 10²³ atoms of Cu and weighs 63.546 grams Happy Mole Day to all the scientists and chemistry enthusiasts! #moleday #chemists #avogadro

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  • Unternehmensseite von Solvias anzeigen, Grafik

    13.586 Follower:innen

    Pyrogen testing is essential for the safety of parenteral products and medical devices, preventing life-threatening fever reactions induced by pyrogenic substances. The Monocyte Activation Test (MAT) is a step forward in ensuring patient safety, regulatory compliance, and ethical testing practices: 🐰Unlike the Rabbit Pyrogen Test (RPT), MAT is an animal-free testing method ✔️MAT detects both endotoxin and non-endotoxin pyrogens 🎯 MAT has a lower limit of detection compared with the Rabbit Pyrogen Test (RPT) 💉MAT is suitable for a range of drug products, especially parenteral drugs and biologics Interested in learning more about how MAT can benefit your products? Contact us at info@solvias.com.

  • Unternehmensseite von Solvias anzeigen, Grafik

    13.586 Follower:innen

    Wrapping up our interview series from Research Triangle Park (RTP), we're proud to feature Anamica Sriram Muruganandham, our Director of Molecular Biology Services. Anamica highlights how our advanced integrated LIMS (Laboratory Information Management System) and ELN (Electronic Lab Notebook) streamline laboratory operations, improve data management, and elevate the overall quality of our services. 📽️ Watch Anamica's insights in the full interview below! 👇

  • Unternehmensseite von Solvias anzeigen, Grafik

    13.586 Follower:innen

    Last month, the FDA released a new guidance on the “Control of Nitrosamine Impurities in Human Drugs”, updating their 2021 recommendations. The guidance covers: 🔬 Root Causes of Nitrosamine Formation – including small molecule nitrosamines and nitrosamine drug substance-related impurities (NDSRIs) 📊 Control & Mitigation Recommendations – for both APIs and drug products ✔️ Acceptable Intake Limits – with guidance on testing, risk assessment timelines, and necessary regulatory submissions Ready to stay ahead of evolving regulations? Solvias provides rapid nitrosamine screening and development/validation of control methods for small nitrosamines, NDSRIs, and any other genotoxic impurities with unparalleled sensitivity and selectivity. We utilize well-established GC/MS/MS and LC/MS/MS methods which showcase exceptional accuracy, consistently delivering outstanding performance within the low parts-per-billion thresholds mandated by regulatory authorities. Contact us at info@solvias.com to learn more

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  • Unternehmensseite von Solvias anzeigen, Grafik

    13.586 Follower:innen

    What an incredible time at #CPHI2024 in Milan! We had the pleasure of connecting with so many inspiring professionals and discussing how to accelerate innovation in the pharmaceutical industry. A huge thank you to everyone who stopped by booth 7G116 to meet with Nicole Hendriks, Norberto Bonalumi, Vania Santana, Juergen Rotzler, Stefan D., and Charlie Brault, MPS. Missed us at CPHI? Don’t worry—you can still reach out to our team for follow-up meetings. We’re here to help bring your innovation to its destination! #CPHIMilan

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