Gene editing in 2025: from CRISPR to next generation platforms

Explore how gene editing is evolving beyond CRISPR with base editing and prime editing technologies shaping next generation therapeutics.
AI Drug Discovery: The Future of Small Molecule Design

Discover how AI drug discovery is reshaping small molecule design through faster learning cycles, better prediction, and integrated decisions.
Accelerating Your Success in Antibody Discovery and Engineering

Syngene provides multi-platform antibody discovery and optimization services to drive faster progression from hits to lead candidates.
Direct to Biology for Drug Discovery Acceleration: Syngene’s D2B Platform
Publication: Pharmaceutical Technology Focus
Tirbanibulin and targeted dermal delivery in topical drug development

Tirbanibulin shows how ADME science, dermal delivery, and topical formulation development turn
skin drugs into real therapies. Read the full Syngene perspective now.
Therapeutics 2.0: Veterinary Oncology and Peptide Conjugates for Companion Animal Health

Explore how peptide conjugates are advancing veterinary oncology and pet therapeutics through targeted drug delivery. Discover emerging approaches today.
Current Toxicology Developments: Advancing Digital Pathology in Predictive, Mechanistic, and Human-Relevant Safety Science

Explore how digital pathology is transforming predictive toxicology and safety assessment. Learn the latest approaches in modern toxicology—read more now.
Your one-stop-shop for XDCs

Syngene offers an integrated bioconjugation platform for XDCs, providing end-to-end support from antibody discovery to GMP manufacturing at up to 1 kg scale. Their expertise covers diverse conjugation technologies, payload and linker chemistry, and advanced analytical and bioassay support. Syngene ensures single-source manufacturing of antibodies, peptides, oligonucleotides, payloads, and linkers, minimizing risk and delays.
Speed vs. quality: balancing timelines in outsourced R&D with GXP compliance

How pharma teams balance speed and GXP compliance in outsourced R&D to deliver predictabletimelines and regulatory-ready outcomes. Explore the approach.
Peptides in the pipeline: How companies are overcoming the early-stage challenges
Publication: Pharmaceutical Technology Focus