Bridging the gap between lab-scale discovery and GMP reality. We provide the independent vetting and on-ground governance required to navigate India’s ecosystem with absolute certainty. We offer the full small molecule lifecycle-from target validation and early discovery through IND-enabling studies, CMC, and commercial manufacturing.
Chiral Synthesis (Asymmetric), Catalysis, Organometallics, & High-Pressure Reactions.
Azide Chemistry, Nitration, Halogenation, & Cryogenic Reactions ($-78^{\circ}C$).
Preparative HPLC, Chiral Resolution, & Simulated Moving Bed (SMB) Chromatography.
Polymorph Screening, Salt Selection, & Micronization Oversight.
Expert partner scouting and technical vetting for medicinal chemistry programs.
High-level advisory for hit-to-lead (H2L), lead optimization, and SAR studies.
Oversight of complex molecule synthesis including libraries, analogs, and reference standards.
Consultation on FTE (Full-Time Equivalent) models and IP-secure vendor selection.
"Access world-class in vitro platforms and robust target validation capabilities."
Platform Identification: Vendor scouting for specialized in vitro assays, target validation, and biomarker studies.
Assay Oversight: Technical management of assay development/transfer and rigorous data integrity verification.
Screening Qualification: Partner vetting for biochemical, cell-based, and phenotypic screening platforms.
Lead Profiling: Expert guidance on early hit validation and selectivity profiling to ensure candidate quality.
The Aventiq Edge: Independent reproducibility audits that ensure your lead compounds are built on a foundation of flawless, verifiable biological data.