CDMO & BPO Solutions | GMP Manufacturing & Biotech Process Services | Chemigran

    Partner with Chemigran for end-to-end CDMO services: custom synthesis, process optimization, and GMP-scale production. Sustainable, scalable, and regulatory-compliant across pharma, biotech, and agritech.

    From Molecule to Market – Partner with Chemigran​

    Chemigran is more than a supplier — we’re your end-to-end CDMO and biotech process outsourcing (BPO) partner.

    From Molecule to Market – Partner with Chemigran

    With 30+ years of experience in custom synthesis, regulatory compliance, and eco-efficient manufacturing, we help pharmaceutical and biotech innovators take products from bench to batch, from reference standard to full-scale API.

    Our Services

    Preclinical & Development

    - Custom API & impurity synthesis
    - Route scouting & process development
    - Analytical method development (HPLC, NMR, MS)
    - Impurity profiling per ICH Q3A/B

    Pilot & Scale-Up

    - Small-to-mid scale GMP batch production
    - Process validation & optimization
    - Regulatory documentation (CoA, MoA, DMF)
    - Batch-specific impurity & stability studies

    Commercial Manufacturing

    - Exclusive or contract manufacturing
    - Supply chain management (GMP-sourced materials)
    - Regulatory support for CTD, ANDA, 505(b)(2)
    - Ongoing batch supply under CDMO agreement

    Biotech Process Outsourcing (BPO)

    - Fermentation trials for biopharma or agritech
    - Microbial testing and CRISPR-enhanced strain validation
    - ESG & GRI-tracked lab process outsourcing
    - Data-driven insights via Chemigran’s IRTA platform

    Built for High-Impact ​Molecules

    • Oncology APIs (e.g., Etoposide, Anthracyclines, Alkylating agents)

    • Rare & Orphan Disease Intermediates

    • Hormonal & CNS APIs

    • Natural Product & Semi-Synthetic APIs

    • Biotech-grade agricultural compounds (probiotics, biostimulants)

    From small-scale validation to GMP commercial batch production, we offer unmatched agility for niche, high-value APIs.

    Sustainability is Our ​Standard

    Regulatory & Documentation Excellence

    We work backwards from submission — not just from chemistry:
    Certificate of Analysis
    Batch Records & MoA
    ICH Q3A/B Impurity Profile
    GMP Compliance Audit Trail
    DMF (Open & Closed Part)
    CTD Section Support

    Ready to Scale Your Molecule?

    Let’s take your molecule beyond R&D.

    Whether you need a full CDMO solution or want to outsource specific process steps, Chemigran is your trusted biotech partner.

    Contact Us

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