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Unlocking New Possibilities in Bioconjugate Innovation. Connect with Our Experts at World ADC San Diego - Booth No 16.
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In today's competitive pharmaceutical landscape, speed and precision are crucial for transforming promising concepts into viable drug candidates. Yet, the path from hit identification to optimized lead is often hindered by complex structure–activity relationship (SAR) studies, demanding synthesis requirements, and iterative cycles of testing and refinement.
Oct 31, 2025
Oral Solid Dosage (OSD) forms – such as tablets and capsules – remain the backbone of modern pharmaceuticals. They are stable, scalable, and preferred by patients for their convenience and ease of administration.
Oct 28, 2025
For decades, Contract Development and Manufacturing Organizations (CDMOs) have been valued primarily for their expertise in chemistry and processes, alongside specialized skills in scale-up, synthesis, and compliance. But as the pharmaceutical landscape becomes increasingly complex and patient-centered, the expectations placed on CDMOs are rapidly evolving.
Oct 24, 2025
In the race to bring new therapies to market, active pharmaceutical ingredient (API) development is often where timelines are made or lost. Efficient synthesis, scalability, and regulatory readiness all hinge on one critical step: identifying the most effective route of synthesis.
Oct 16, 2025
Antibody-Drug Conjugates (ADCs) have rapidly emerged as one of the most promising therapeutic classes in pharmaceuticals, particularly in oncology. By combining the targeting power of monoclonal antibodies (mAbs) with the potency of cytotoxic payloads, ADCs offer precision treatment options with reduced off-target effects.
Oct 13, 2025
