IDAIB Offers wide range of services to suit your needs

API Bulk Production

We specialize in bulk synthesis of Active Pharmaceutical Ingredients (APIs) under stringent quality conditions.

Our chemists deliver compounds with high purity, stability, and reproducibility, serving pharmaceutical, academic, and biotech clients.

Capabilities:
Multi-step organic synthesis and scale-up
GMP / non-GMP API manufacturing
Impurity profiling, isolation, and reference standard supply
Analytical validation using HPLC, GC-MS, NMR, and LC-MS/MS

Our pure chemistry division focuses on designing, synthesizing, and purifying compounds to support R&D and regulatory submissions.

We offer:
Custom synthesis of intermediates, impurities, and metabolites
Structure elucidation and spectral characterization
Small molecule libraries and analog development
Impurity marker synthesis for quality control

Our in vitro testing platform supports mechanistic and cytotoxicity evaluations for drug candidates.

Capabilities:
Cell-based assays (e.g., MTT, apoptosis, migration)
Cytokines and tumor marker estimation
High-throughput compound screening and data analytics.

Pure Chemistry & Impurity Synthesis

In Vitro Screening

API Bulk Production

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Our in-vivo research division provides validated preclinical models to assess safety and efficacy.

Expertise:
End-to-end preclinical protocol design, validation, and execution
Tumor xenograft and syngeneic models
Pharmacokinetic and toxicological studies
Immunological profiling (CD3, Tregs, IHC, ELISA)
Histopathology analysis

All studies are conducted under ethical and regulatory guidelines, ensuring reliability and reproducibility.

In Vivo Screening

From target identification to preclinical validation, we provide a seamless pipeline that bridges chemistry and biology.

Hit identification & lead optimization
Mechanistic and efficacy evaluation
Data documentation for IND-enabling studies
Collaborative partnerships with CROs and academic labs

Integrated Drug Discovery Support