Announcement under Regulation 30 (LODR)-Credit Rating 14 Oct - ICRA assigned [ICRA]AA+ (Stable) rating to proposed ₹1,400 crore non-convertible debentures.
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Pharma stocks · Large cap · NSE
Jubilant Pharmova is an integrated global pharmaceutical company with businesses in Radiopharma, Allergy Immunotherapy, CDMO Sterile Injectables, CRDMO, Generics, and Proprietary Novel Drugs. It operates 45 radiopharmacies in the US and serves top global innovators with a team of 5,500 people.
SMA20 +5.0% / mo · MACD − · sector +3.8pp vs Nifty 500 (3M)
FPI equity flow was positive in both fortnights, but the sector index is below its 100-session average. View sector evidence
Adjusted completed-session prices, rebased to 100
Weak fundamentals, while price trend supports entry. This looks more like momentum/speculation than a clean fundamental investment setup.
Weak U-Score but strong trend: momentum may be ahead of fundamentals.
Fundamental lens: valuation, quality, growth, balance sheet, and cash flow.
Revenue +17.3% · PAT -45.1% YoY
Price trend and sector-relative-strength timing.
Legacy margin-of-safety estimate; the revised evidence label remains in shadow validation.
Financial-only signal; management claim evidence is not sufficient yet.
Fundamentals, quarterly history, margins, returns and balance-sheet evidence
PAT -45% YoY · margin compression · Rev +17% YoY
| Metric | This quarter | YoY | QoQ |
|---|---|---|---|
| Revenue | ₹2,229 Cr | +17.3% | -2.7% |
| EBITDA | ₹248 Cr | -14.5% | -26.8% |
| Operating margin | 11.0% | -400 bps | -400 bps |
| PAT | ₹56 Cr | -45.1% | -52.9% |
| PAT margin | 2.5% | -286 bps | -269 bps |
NDF means not disclosed in the current structured filing feed. It is intentionally not treated as zero.
Updated 20/10/2026
Trend interpretation, Stage 2, relative strength, volume and indicator evidence
Signals are conflicting — long-term trend down. RSI 39. Wait for confirmation.
Mechanical read from the price + indicator series above. Not a recommendation — technical setups can reverse without warning, especially around earnings and macro events.
U-Score 24 · legacy U-Score band OVERVALUED · valuation evidence and comparable companies
Top U-Score contributors and drags from the latest stored fundamentals.
Healthcare valuation needs both earnings quality and regulatory/pipeline context.
This shows the stored score trend when snapshots exist, and also compares the latest stored nightly score with a live recompute from current fundamentals and price.
12 stored score snapshots. Latest stored move: +0 points.
Business-comparable peers in Pharma — ranked by industry, sub-sector, theme-tag overlap, market cap, and U-Score similarity. Green cells mark the best available peer metric in this table.
Growth engines, risks, management commitments and evidence-backed delivery
FY26 revenue grew 14% YoY to Rs. 8,280 Cr, driven by CDMO Sterile Injectables. EBITDA grew 8% YoY to Rs. 1,326 Cr, but margins declined due to temporary production issues at the Montreal facility. Normalised PAT increased 7% YoY.
The company's strategy of investing in specialty products and services, particularly CDMO Sterile Injectables and Radiopharma, is yielding revenue growth. However, operational challenges at the Montreal facility are temporarily compressing margins. Management's plan for margin recovery from H2'FY27 and ongoing capacity expansions are critical for thesis validation.
Latest issuer-disclosed distribution across 5 reported categories.
Achieved one of the fastest revenue ramp-ups in the industry, onboarding a world's largest oncology product.
Install base grew 35% in FY26, demonstrating superior value proposition and increasing EBITDA margins.
US$50 million investment to expand from 3 to 9 sites by FY28, strongly positioning the network for future growth.
Delivered strong growth (13% YoY) and double-digit operating profitability (EBITDA margin up 7.2 percentage points) in FY26.
Launched in Q2'FY26, successfully ramping up technology transfer revenues. Commercial batch production expected late FY27.
Installation on track, expected to start generating technology transfer revenues by Q4'FY27.
New isolator-based fill-and-finish line under construction, expected to generate revenues from FY29 onwards.
Proposed investment of US$50 million to expand from 3 to 9 sites in the US by FY28.
Global CDMO-SI market demand-supply gap is widening, with a projected 700 Mn vials by 2027.
Large innovator pharma companies are increasingly seeking high-quality, US-based manufacturing due to new US tariffs.
Driven by new PET imaging products and advanced therapies, with multiple billion-dollar M&A deals in the sector.
India is uniquely positioned to benefit from friendshoring, with rising interest in specialized technologies like ADCs in CRDMO.
Temporary shutdown of CDMO Sterile Injectables facility in Montreal for remediation, impacting Radiopharma SPECT production and overall EBITDA margins.
Industry-wide pricing pressure continues to affect the API business, leading to decreased revenue and EBITDA margins in FY26.
Management expects competitive intensity to increase in the large-pharma customer segment in the short term.
Temporary shutdown of Montreal facility due to FDA observations highlights the risk of regulatory non-compliance impacting production and financial performance.
Timely commissioning, FDA approvals, and successful ramp-up of new lines (Spokane Line 3/4, Montreal Line 5, PET facilities) are critical for future growth.
Continued industry-wide pricing pressure, particularly in the API and potentially Generics segments, could hinder profitability and revenue growth.
Issuer guidance and extracted claims are tracked against later reported outcomes. Treat these as management statements, not IndiaPulse forecasts.
YoY comparison is essential for assessing overall financial health and annual trends across seasonal pharma segments. QoQ is crucial for monitoring sequential momentum, especially for the ramp-up of new CDMO lines and the recovery of the Montreal facility.
Generics business revenue grew 13% YoY in FY26.
US market constitutes 80% of FY26 revenue. CDMO Sterile Injectables (Spokane) revenue grew 48% YoY in FY26.
Radiopharma plans 7 new PET/SPECT products from FY28-FY29. Generics launched 4 new products in the US in FY26.
Commercial batch production for Spokane Line 3 expected late FY27, subject to FDA approval. MIBG NDA filing expected by H2'FY27.
Aims to double revenues to Rs. 13,500 Cr, achieve 23-25% EBITDA margin, and zero net debt by FY30.
Expects EBITDA margins to strengthen from H2'FY27 onwards, post stabilization of production at the Montreal facility.
Announced a strategic partnership with Pierre Fabre to expand CRDMO footprint in Europe for biologics (mAbs) and Antibody-Drug Conjugates (ADCs).
Combined drug discovery and API businesses into "Jubilant Biosys" to improve operational efficiency and enhance brand recall for end-to-end CRDMO services.
| Checkpoint | Current evidence | What to verify next |
|---|---|---|
| Montreal Facility Production Stabilization | Temporary shutdown, under-absorption of costs. | Resumption of commercial batch production in Q1'FY27 and normalization of revenue/EBITDA from H2'FY27. |
| Spokane Line 3 Commercial Batch Production | Ramping up technology transfer programs. | Commencement of commercial batch production in late FY27 and progress towards full utilization. |
| PET Manufacturing Network Expansion | Investment underway to expand from 3 to 9 sites. | Timely commissioning of new facilities by FY28 and associated revenue ramp-up. |
| API Custom Manufacturing Mix | Revenue mix shifting towards profitable products. | Increase in custom manufacturing revenue mix in FY27 to drive utilization and improve margins. |
Verification checkpoints are IndiaPulse research interpretation, not investment advice.
Trust asks: does management behaviour match later outcomes? Higher is better, but confidence and evidence depth matter as much as the number.
Limited evidence: Claim history is still being built. It ranks around the 49th percentile of the scored universe and 36th percentile within Pharma. Main check: results consistency is weak at 39/100.
This is a financial-behaviour screen, not a claim-tested management reliability verdict.
Financial behaviour is scored, but management claims do not yet have enough outcome checks.
overall median 67 · Pharma: 36th pctile, median 70 · Large: 26th pctile, median 73
80 documents have extracted text, but claim history is not strong enough yet.
0 claims extracted · No contradicted claim yet
Read Trust alongside U-Score, result consistency, and technical trend. A cheap stock with weak Trust needs a larger margin of safety; a high Trust score does not make an expensive stock attractive by itself.
Read low sub-scores as due-diligence warnings, not automatic sell signals.
Trust Lite uses financial behaviour only. Prefer claim-tested Trust when enough concall claims have later outcomes.
Latest exchange and company disclosures found within the past two years.
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