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CDMO red flags you can’t ignore: Capacity constraints and resource stretch

Part 4: When “Too Busy” Becomes a Business Risk Even the most capable CDMO cannot deliver high-quality work if it is stretched too thin. As demand for outsourcing continues to rise across the life sciences sector, many CDMOs are operating near or beyond capacity. For pharma and biotech companies, this creates a silent but serious […]

Whitepaper

26.11.25

5 CDMO red flags you can’t ignore: A guide for biotechs and pharma

Selecting the right CDMO is one of the most important choices a biotech or pharma team will make. The right partner helps you move efficiently toward IND or IMPD, safeguard quality, and anticipate regulatory needs before they become roadblocks. The wrong one can mean delays, rising costs, and lost momentum. At Exemplify BioPharma, a Symeres company, […]
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Whitepaper

09.07.25

Accelerating chemical innovation: Unveiling Symeres’ parallel chemistry

By combining automation, data-driven design, and deep synthetic expertise, Symeres is redefining how chemists generate and optimize compound libraries, bringing speed, scalability, and creativity to modern drug discovery.
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Whitepaper

08.07.25

IND & IMPD enabling developability roadmap

Drug discovery and development is a complex and iterative process that involves the identification, design, development, testing, and approval of new pharmaceutical drugs for use in patients. It encompasses a series of scientific, regulatory, and commercial activities aimed at discovering and bringing safe and effective medicines to the market. A key milestone in this process […]
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Whitepaper

07.07.25

Innovations in unnatural amino acids: Advancing functional diversity and applications

Unnatural amino acids enable groundbreaking advancements in drug discovery, biomaterials, and peptide design by introducing novel chemical functionalities that enhance stability, specificity, and bioactivity. This whitepaper highlights Symeres’ expertise in synthesizing unnatural amino acids, including side-chain modifications, N-functionalization, and cyclic variants, for applications in pharmaceuticals, diagnostics, and materials science. Utilizing advanced techniques like biocatalysis and […]
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Whitepaper

06.07.25

Leveraging copper-catalyzed ullmann-type cross-coupling reactions in PR&D

Our experience in overcoming scaleup challenges and harnessing the benefits of non-noble-metal catalysis makes Symeres the CRO of choice for challenging steps, such as the Ullmann reaction.
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Whitepaper

05.07.25

Managing nitrosamines in the pharmaceutical industry: A comprehensive approach

A comprehensive overview of nitrosamine risk assessment, including potential formation, scavenging, and analysis, is described here.
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Whitepaper

04.07.25

Optimizing solid-state properties and enhancing API bioavailability through physicochemical prediction

Here at Symeres, we have our new ‘Solid-State Center of Excellence’, and in this whitepaper we describe how we utilize our expertise and novel innovation to further our solid-state capabilities.
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Whitepaper

03.07.25

Stable isotope-labeled compounds

Discover how Symeres applies advanced synthetic chemistry and ADME expertise to design, produce, and study stable isotope-labelled compounds that enhance precision in drug development.
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Whitepaper

01.07.25

Unlocking the potential of high-throughput screening: Symegold library design and expansion insights

Learn how Symeres combines advanced chemistry platforms and deep discovery expertise to design and expand the SymeGold library, driving more efficient high-throughput screening and smarter hit identification.
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