Financial Performance Summary
Quarterly Performance (Q2 FY27 vs Q2 FY26):
- Revenue from Operations: ₹8,741.61 lakhs (vs ₹5,756.04 lakhs) - 53% YoY growth
- Gross Profit: ₹4,168.05 lakhs (vs ₹2,715.40 lakhs) - 53% YoY growth
- Gross Profit Margin: 48% (vs 47%)
- EBITDA: ₹2,434.53 lakhs (vs ₹1,135.39 lakhs) - 114% YoY growth
- EBITDA Margin: 28% (vs 20%)
- Profit After Tax: ₹1,130.69 lakhs (vs ₹453.98 lakhs) - 149% YoY growth
- PAT Margin: 13% (vs 8%)
Half-Yearly Performance (H1 FY27 vs H1 FY26):
- Revenue from Operations: ₹16,038.86 lakhs (vs ₹11,029.66 lakhs)
- Gross Profit: ₹8,007.08 lakhs (vs ₹5,093.78 lakhs) - 57% YoY growth
- Gross Profit Margin: 50% (vs 46%)
- EBITDA: ₹4,559.42 lakhs (vs ₹2,405.97 lakhs) - 90% YoY growth
- EBITDA Margin: 28% (vs 22%)
- Profit After Tax: ₹2,159.18 lakhs (vs ₹921.11 lakhs) - 134% YoY growth
- PAT Margin: 13% (vs 8%)
Business Highlights and Operational Metrics
Regulatory and Commercial Progress:
- Executed 69 oncology product contracts with 45 commercial discussions underway
- Shared 351 dossiers globally, with 191 submitted to regulatory agencies
- 22 Marketing Authorizations (MAs) granted globally:
- Europe & UK: 11 MAs
- Latin America: 6 MAs
- APAC: 4 MAs
- Canada: 1 MA
- Completed 36 EU MA applications including 16 own filings
- Submitted 33 site variations covering 18 cytotoxic molecules
- 11 site variation approvals received in stringent markets of EU and UK
Technology and Development:
- 33 technology transfer projects for oncology products underway with 4 partners
- Developed 21 APIs in-house including:
- 16 APIs with Written Confirmation
- 8 commercialized products
- 2 of 7 CEP applications approved with 5 in process
Facility and Supply Chain:
- Commercial supplies commenced from API-integrated, EU GMP-approved oncology FDF site
- Accord received 6 more product site variations approval by EMA (total now 8 of 11 molecules)
- 3 additional site variation approvals from MHRA/EMA for partners in UK and Germany
Product Portfolio:
- Coverage expanded to cancers of breast, lung, prostate, stomach, head & neck, colorectal, ovary, liver, kidney, thyroid, blood, bone-marrow and lymph
Management Commentary
Mr. Sanjay Shah, Managing Director, commented:
- Q2 FY27 represented meaningful progress for oncology business with encouraging developments across regulatory approvals, technology transfers and global market access
- Commencement of commercial supplies from EU GMP-approved, API-integrated oncology facility marks an important milestone
- In-house API capabilities and ongoing technology transfers are strengthening the integrated platform
- Enhanced supply-chain control and expanded ability to serve regulated markets
- Optimistic about opportunities from expanding oncology portfolio, growing pipeline and international partnerships
- Expects these developments to support export growth, improved capacity utilization and operating efficiencies
- Positions company for sustainable, long-term growth
Company Background
Sakar Healthcare Limited, established in 2004 and headquartered in Ahmedabad, Gujarat, is a publicly listed pharmaceutical manufacturer and exporter specializing in:
- Oncology
- Antibiotics
- General formulations
Operates world-class, EU-GMP and WHO-GMP certified facilities manufacturing:
- Oral solids
- Injectables
- Oral liquids
- High-potent oncology products
Oncology division at Bavla represents research-driven, API-integrated facility focused on developing and commercializing complex cytotoxic formulations and APIs
Global footprint across more than 60 countries serving multinational pharmaceutical companies through:
- CDMO collaborations
- CRAMS partnerships
- Technology transfer collaborations
Driven by vision to deliver world-class healthcare solutions with strong R&D capabilities, regulatory excellence, and sustainable manufacturing practices rooted in green chemistry principles.