Insights On CONTRACT PHARMA MANUFACTURING
-
Class 3 Atropisomers: Capture Therapeutic Selectivity In Oncology
11/26/2025
Atropisomers are key to modern small molecule drug development. Learn how advanced manufacturing strategies enable the isolation and scalable production of the most effective single isomer.
-
Every Medicine Has A Story. We Help You Write Yours.
11/26/2025
We are a leading global CDMO with a network of cGMP facilities in key markets. From early development to commercial scale, we handle the manufacturing and testing that help your therapies take the next step.
-
Framework To Deliver Standardized, Reliable Biomanufacturing Facilities
11/25/2025
Standardized, continuously optimized facility design enables scalable, efficient, and reliable biomanufacturing that improves quality, accelerates timelines, and ensures consistent performance across sites.
-
Accelerated LVV Manufacturing Enabled By Platform Excellence
11/25/2025
Discover how a manufacturing platform enabled the rapid production of lentiviral vector in eight months. Learn the strategy used to balance speed, risk mitigation, and the highest quality standards.
-
Efficient Late-Stage Development Of Biologics
11/25/2025
Reducing biologics manufacturing costs requires strategic late-stage process development, yield optimization, scale-up, and raw material substitution—all while maintaining product quality and regulatory compliance.
-
Quality By Design Meets Digital QMS In Advanced Therapies
11/25/2025
Risk-based quality systems, proactive problem-solving, and collaborative client relationships drive operational excellence, supported by digital QMS tools for compliance, deviation management, and continuous improvement in biomanufacturing.
-
Comparing Gel, qPCR & HPLC For DNA/RNA Analysis
11/25/2025
Cost-effective agarose gel electrophoresis offers reliable plasmid supercoil and host DNA/RNA quantification, providing a practical alternative to qPCR and HPLC for biomanufacturing quality control.
-
Production Site Brno (CZ) Clinical/Commercial Syringe Line
11/24/2025
Gain access to specialized sterile injectable manufacturing. Expertise covers vials and modern pre-filled syringe capacity, supported by single-use systems and decades of proven quality for global markets.
-
Controlled Nucleation Offers Homogeneity And Batch Consistency
11/24/2025
Controlled nucleation standardizes freezing across all vials, leading to uniform ice crystals and improved lyo cake quality. This critical step reduces variability and supports robust product scale-up.
-
How To Choose The Right CDMO Partner For Fill & Finish
11/24/2025
CDMO selection requires evaluating experience, quality standards, and flexibility. Assess technical transfer skills, supply chain security, and collaborative approach for a reliable, long-term project fit.