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Medac GmbH Advances Pharmacovigilance Technology for Safety Monitoring of its Drugs with ArisGlobal Solutions

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ArisGlobal, a market-leader in global drug development technology solutions, announced that medac, a German-based pharmaceutical manufacturer specializing in the fields of oncology and hematology, urology, and autoimmune diseases, has chosen LifeSphere Safety to modernize its drug safety processes. Precise, patient- and population-specific analysis is crucial for minimizing treatment risks for patients and thus supports the best possible treatment outcome.

โ€œArisGlobalโ€™s Safety solutions will significantly advance the automatization of adverse event management and intelligent safety analysis and will support us in making pharmacovigilance processes even smarter and more efficient,โ€ said Doctor Nadine Schreiber, Head of Global Pharmacovigilance of medac.

medac will launch three products from LifeSphere Safety, including its flagship solution for automated case processing, LifeSphere MultiVigilance, along with Reporting and Analytics, and EV Triage.

โ€œLifeSphere has been developed with organizations like medac in mind; to meet global compliance, provide next-level safety insights, and operate with greater efficiency,โ€ shares Aman Wasan, Chief Commercial Officer, ArisGlobal. โ€œWe are pleased that medac has entrusted LifeSphere products to continue their advancement of therapeutic development processes. We are confident that medac will see incredible benefit to onboarding these solutions and positively impact safety analysis at scale.โ€

Visit ArisGlobal at the 2023 World Drug Safety Congress Europe (Booth 19) and Americas (Booth 202) to learn more about LifeSphere Safety and Data & Analytics solutions.
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Advanced Color Measurement Strengthening Pharma QC

Achieving absolute precision in pharmaceutical manufacturing necessitates a comprehensive and rigorous oversight of physical attributes, with color serving as a primary indicator of chemical stability and composition. By integrating sophisticated instrumentation into the laboratory environment, manufacturers can transition from subjective visual assessments to standardized, data-driven methodologies that satisfy the most stringent global regulatory requirements. This strategic focus on color measurement pharma QC facilitates the early identification of raw material impurities and ensures uncompromising batch-to-batch consistency in final dosage forms, thereby bolstering patient safety and brand reputation.

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