Capabilities
What We Do
Mac-Chem manufactures active pharmaceutical ingredients across three segments, Oncology API, Lyophilized Bulk Sterile API, and General API, from a single CGMP-compliant plant in Boisar, Maharashtra.
Oncology API 15,000 kg/yr · Lyophilized Bulk Sterile API 15,000 kg/yr · General API 10,000 kg/yr installed capacity
Installed capacity
Three API segments, one Boisar site
Installed annual capacity across Mac-Chem's three API segments, as published in the company's own capacity register.
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15,000 kg/yr
Oncology API capacity
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15,000 kg/yr
Lyophilized Bulk Sterile API capacity
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10,000 kg/yr
General API capacity
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41
R&D & analytics scientists
Product mix
What the plant actually produces
Mac-Chem's 63-product API catalog spans oncology and non-oncology therapeutic areas, backed by DMF and CEP dossiers. Every count below is drawn live from the product catalog.
| Therapeutic area | Products | Share of catalog |
|---|---|---|
| Oncology | 33 | 52% |
| Anti-infective | 9 | 14% |
| Anesthesia | 9 | 14% |
| Supportive care | 6 | 10% |
| Hormonal | 5 | 8% |
| Other therapeutic area | 1 | 2% |
| Total catalog | 63 | 100% |
Source: API catalog (63 products, live count). Every ingredient also carries a regulatory filing (DMF / CEP). See API Products for the filterable catalog.
By capability
Four ways into the plant
Manufacturing is the base capability everything else builds on; lyophilization is the specialization behind Mac-Chem's Lyophilized Bulk Sterile API segment; R&D covers the non-infringing process development behind the catalog and its pipeline. Quality & Regulatory governs what the plant is permitted to ship, and where.
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Manufacturing
The Boisar (Tarapur MIDC) production floor behind Mac-Chem’s 63 marketed APIs across three segments — Oncology API, Lyophilized Bulk Sterile API, and General API — run under GMP-compliant, GAMP-controlled process controls.
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Lyophilization
Freeze-drying capacity purpose-built for the Lyophilized Bulk Sterile API segment (15,000 kg/yr), the specialization behind Mac-Chem’s "Pioneers in Lyophilization" line.
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Research & Development
Non-infringing process development behind the marketed catalog and its in-development pipeline, run through a DSIR-approved R&D lab with 41 scientists in synthesis and analytics.
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Quality & Regulatory
Six documented accreditations, all confirmed from certificates on file: India GMP, WHO-GMP, EDQM CEP, Swissmedic, CDSCO Written Confirmation, and ISO 14001/45001.