Gufic Biosciences Limited (GUFICBIO)
₹404.50 -0.97% last close, 16 Oct
Latest quarterly results (Q1 FY27)
In its latest reported quarter, Q1 FY27, Gufic Biosciences' revenue was ₹261 Cr (+16.6% year on year, +3.5% on the previous quarter), and net profit ₹22.3 Cr (+70.7% year on year); the operating margin was 17.9%.
| Q1 FY27 (₹ Cr) | Value | YoY vs Q1 FY26 | QoQ |
|---|---|---|---|
| Revenue | ₹261 | +16.6% | +3.5% |
| Operating profit | ₹46.6 | +40.0% | -0.8% |
| Net profit | ₹22.3 | +70.7% | +1.4% |
| EPS (₹) | 2.22 | +70.8% | +1.8% |
| Operating margin | 17.9% | — | — |
GUFICBIO delivery percentage
NSE end-of-day data for
On Fri, 16 Oct 2026, 62.69% of the GUFICBIO shares traded on NSE were taken to delivery, against the stock's own 20-session average of 52.59%. Delivery was unusually high while the price barely moved (-0.97%). Volume was 0.3 times its average, well below normal.
Delivery in the last 5 sessions: 59.6% · 57.5% · 55.9% · 32.3% · 62.7%
A description of what the exchange published, not a recommendation. Names such as "accumulation" or "long buildup" label a pattern in the numbers. How delivery is analysed
📢 Recent Corporate Announcements
Gufic Biosciences has submitted its quarterly compliance certificate under Regulation 74(5) of the SEBI (Depositories and Participants) Regulations, 2018 for the quarter ended September 30, 2026. The certificate from RTA MUFG Intime India Private Limited confirms that share certificates received for dematerialisation during the quarter were processed, confirmed or rejected, and mutilated within prescribed timelines. This is a standard quarterly administrative filing with no impact on business operations or financials.
- Regulation 74(5) compliance certificate submitted for the quarter ended September 30, 2026
- Issued by Registrar and Share Transfer Agent MUFG Intime India Private Limited (formerly Link Intime India)
- Filing submitted to BSE and NSE on October 6, 2026
Gufic Biosciences received a favorable appellate order under Section 250 of the Income Tax Act from the Commissioner of Income Tax (Appeals) on September 29, 2026. The order allows the company's appeal against an income tax demand of ₹4,33,36,680 for Assessment Year 2024-25. The demand had originated from an expenditure disallowance under Section 143. Upon giving effect to the order, the full ₹4.33 crore demand will be deleted, removing a potential liability that equals approximately 5.8% of TTM PAT (₹74 Cr).
- Appellate order dated September 28, 2026 received on September 29, 2026 under Section 250 of the Income Tax Act.
- Income tax demand of ₹4,33,36,680 for AY 2024-25 ruled entirely in favor of the company.
- Order results in the full deletion of the ₹4.33 crore demand arising from expenditure disallowances.
- Relief amount represents approximately 5.8% of the company's TTM PAT of ₹74 crore.
Gufic Biosciences received a rejection from NSE regarding its waiver application for a penalty of ₹1,72,000 (excluding GST) levied for Q2 FY25. The fine was imposed under Regulation 17(1A) for appointing an Independent Director aged over 75 without prior special resolution from shareholders. The company had earlier paid an ₹8,000 penalty for Q1 FY25 and saw a similar waiver rejection by BSE on March 13, 2026. Gufic is now required to pay the ₹1.72 lakh penalty on or before October 03, 2026, which it intends to do.
- NSE rejected the waiver application for a penalty of ₹1,72,000 (excluding GST) on September 23, 2026
- Penalty relates to non-compliance under Regulation 17(1A) for appointing director Kamal Kishore Seth (aged >75) without shareholder special resolution
- Penalty due date is on or before October 03, 2026
- Prior penalty of ₹8,000 (excluding GST) for Q1 FY25 had already been paid to both BSE and NSE
CRISIL Ratings has reaffirmed Gufic Biosciences Limited's credit ratings while enhancing the total rated bank loan facilities from ₹425 crore to ₹516 crore. The long-term rating is reaffirmed at 'CRISIL A-/Stable' and the short-term rating is maintained at 'CRISIL A2+'. The enhancement of ₹91 crore reflects higher working capital or debt headroom relative to the company's existing total debt of ₹405 crore and TTM revenue of ₹981 crore.
- Total bank loan facilities rated enhanced to ₹516 Crore from ₹425 Crore
- Long-term rating reaffirmed at CRISIL A-/Stable
- Short-term rating reaffirmed at CRISIL A2+
Gufic Biosciences Limited announced the voting results and scrutinizer report for its 42nd Annual General Meeting held on September 4, 2026. All five resolutions were passed with over 99.99% majority support across 80,165,607 votes polled (representing 79.94% of total equity shares). Approved resolutions include the adoption of FY26 financial statements, declaration of a 10% final dividend (Rs 0.10 per share of face value Re 1), re-appointment of Director Pranav J. Choksi, and continuation of Pankaj J. Gandhi as Whole Time Director past the age of 70.
- All 5 resolutions passed with over 99.99% majority across total votes polled
- Declared final dividend of 10% (Re 0.10 per equity share of face value Re 1) for FY26
- Special resolution approved for re-appointment of Mr. Pankaj J. Gandhi as Whole Time Director post attaining 70 years of age with 99.9964% votes in favour
- A total of 80,165,607 votes were polled out of 100,282,506 outstanding shares (79.94% turnout)
Gufic Biosciences Limited conducted its 42nd Annual General Meeting on September 04, 2026, via video conferencing. Key resolutions placed for voting included the adoption of FY26 audited financial statements and declaration of a final dividend of Re. 0.10 per equity share (10% of Re. 1 face value). The meeting also considered the re-appointment of Mr. Pranav J. Choksi and the continuation/re-appointment of Mr. Pankaj J. Gandhi as Whole-Time Director. Voting results and scrutinizer reports are scheduled to be disclosed within two working days.
- Concluded 42nd AGM with 43 members attending (5 promoter, 38 public)
- Proposed final dividend of Re. 0.10 per equity share (10%) on face value of Re. 1/- for FY26
- Received 3 corporate representations representing 3,13,60,802 shares (31.27% of paid-up capital)
- Special resolution presented for re-appointment of Mr. Pankaj J Gandhi as Whole Time Director upon attaining age 70
Gufic Biosciences Limited has approved internal promotions for two senior management personnel effective September 02, 2026. Mr. Pinak Padhya, who brings over 28 years of industry experience, has been elevated from Vice President to President – Sales & Marketing. Additionally, Ms. Ami Shah, who has been with the company for over 10 years, has been promoted from Senior Manager – Legal to Head – Legal while continuing her duties as Company Secretary and Compliance Officer. These internal leadership changes are part of standard administrative succession and functional oversight.
- Mr. Pinak Padhya promoted from Vice President to President – Sales & Marketing effective September 02, 2026
- Mr. Padhya holds over 28 years of leadership experience across firms including Sun Pharma, Ranbaxy, and Glenmark
- Ms. Ami Shah promoted to Head – Legal while continuing as CS & Compliance Officer after 10+ years at the company
- Both changes approved by Board via Circular Resolution on September 02, 2026
Gufic Biosciences released the transcript for its Q1 FY27 earnings conference call. Revenue from operations increased 14.9% YoY to ₹260.8 crore from ₹226.9 crore in Q1 FY26, while EBITDA grew 42.2% YoY to ₹47.2 crore, expanding EBITDA margins to 18.09% (vs 14.6% in Q1 FY25-26). Net profit after tax surged 85.6% YoY to ₹22.46 crore compared to ₹12.1 crore in the prior year period. Management highlighted commercial traction for Semaglutide (GLP-1) CMO with partner Hetero across 22 international filings, alongside capability ramp-ups at the Indore facility for complex injectables and liposomal formulations.
- Q1 FY27 revenue from operations rose 14.9% YoY to INR 260.8 crores (vs INR 226.9 crores in Q1 FY26)
- EBITDA increased to INR 47.2 crores with margin expanding to 18.09% (vs 14.6% YoY and 17.74% QoQ)
- Profit after tax grew to INR 22.46 crores (8.61% PAT margin) compared to INR 12.1 crores in Q1 FY26
- Semaglutide (GLP-1) CMO operations with partner Hetero commenced with filings targeted across 22 countries
- Indore facility depot and microsphere suites are nearing completion, targeting operational status in FY27
Gufic Biosciences Limited has informed the stock exchanges that the audio recording of its earnings conference call held on August 17, 2026, at 04:30 p.m. IST is now available online. The disclosure is made pursuant to Regulation 30 of the SEBI Listing Regulations. The company stated that a written transcript of the conference call will be submitted to the exchanges in due course.
- Audio recording of the earnings call conducted on August 17, 2026 at 04:30 p.m. made available online
- Filing submitted in compliance with Regulation 30 of SEBI LODR Regulations
- Written transcript of the concall to be filed in due course
Gufic Biosciences released its Q1 FY27 investor presentation detailing progress at its Indore injectable platform. The plant has designed capacity for 5 million lyophilized vials, 6 million liquid vials, and 10 million ampoules per month, with 203 State FDA approvals received and 40 product tech transfers completed. The company completed an EU GMP audit in December 2025 and is awaiting certification in FY27, while targeting US FDA inspection triggers by FY29. Commercial progress includes the launch of anti-infective AWABAC and completed GLP-1 validation batches for CDMO partners.
- Indore facility capacity stands at 5M lyophilized vials, 6M liquid vials, and 10M ampoules per month (21M units/month total)
- Obtained 203 State FDA product approvals to date, with 40 tech transfers completed and 27 under development
- EU GMP audit completed in Dec 2025 with certification awaited in FY27; US FDA inspection targeted by FY29
- Completed GLP-1 validation batches in Jan 2026 and completed 20+ pharma vendor audits for CDMO business
Gufic Biosciences Limited has approved the incorporation of a subsidiary in the Philippines, proposed as Gufic Philippines Inc., within the next 12 months. The company will invest up to USD 250,000 in cash to subscribe to approximately 99.99% of its equity share capital. The new entity will handle the marketing, sale, distribution, and intellectual property rights management of Gufic's pharmaceutical products in the Philippines. Given the company's TTM revenue of Rs 944 Cr, this initial outlay represents an immaterial financial commitment (<0.3% of annual sales) aimed at establishing a direct Southeast Asian presence.
- Investment of up to USD 250,000 (or equivalent in Philippine Peso) approved for equity subscription
- Gufic Biosciences to hold approximately 99.99% equity shareholding and control
- Incorporation planned within 12 months subject to regulatory approvals
- Proposed entity will manage product marketing, distribution, and local IPR in the Philippines
Gufic Biosciences reported a 70.7% YoY surge in consolidated net profit to ₹22.31 Cr for Q1 ended June 30, 2026, compared to ₹13.07 Cr in Q1 FY26. Consolidated revenue from operations increased by 16.58% YoY to ₹260.82 Cr from ₹223.72 Cr. Basic EPS expanded to ₹2.22 per share against ₹1.30 in the corresponding period last year. Additionally, the board approved the incorporation of a 99.99% owned subsidiary in the Philippines with an initial investment of up to USD 250,000.
- Consolidated Net Profit jumped 70.7% YoY to ₹22.31 Cr (₹2,231.28 Lakhs) in Q1 FY27 vs ₹13.07 Cr in Q1 FY26.
- Consolidated Revenue from Operations grew 16.58% YoY to ₹260.82 Cr vs ₹223.72 Cr in the prior-year period.
- Basic EPS increased to ₹2.22 for Q1 FY27 from ₹1.30 reported in Q1 FY26.
- Board approved incorporation of a 99.99% subsidiary in the Philippines with an investment of up to USD 250,000.
Gufic Biosciences has announced August 28, 2026, as the record date for its 42nd Annual General Meeting and a final dividend of ₹0.10 per share (10% of face value). The AGM is scheduled for September 4, 2026, where shareholders will also vote on the re-appointment of Mr. Pankaj J. Gandhi as Whole Time Director for a five-year term. The proposed remuneration for the director is capped at ₹1 crore per annum. This follows a fiscal year (FY26) where the company reported a net profit of ₹64.3 crore on a revenue of ₹944 crore.
- Final dividend of 10% (₹0.10 per equity share of ₹1 face value) proposed for FY 2025-26
- Record date for dividend eligibility and AGM participation fixed for August 28, 2026
- 42nd Annual General Meeting to be held via video conferencing on September 04, 2026
- Proposed re-appointment of Mr. Pankaj J. Gandhi as Whole Time Director with a salary cap of ₹1,00,00,000 per annum
- Book closure period scheduled from August 29, 2026, to September 04, 2026
Gufic Biosciences has scheduled its 42nd Annual General Meeting (AGM) for September 04, 2026, via video conferencing. The board has recommended a final dividend of ₹0.10 per equity share (10% of face value) for FY26, with a record date of August 28, 2026. Key agenda items include the re-appointment of Mr. Pankaj J. Gandhi as Whole Time Director for a five-year term with a salary cap of ₹1 crore per annum. Additionally, the company is seeking ratification for cost auditor remuneration of ₹4 lakh for FY27.
- Final dividend of ₹0.10 per equity share (10% of face value) proposed for the financial year ended March 31, 2026
- Record date for dividend eligibility and AGM participation set for August 28, 2026
- Proposed re-appointment of Mr. Pankaj J. Gandhi as Whole Time Director for a 5-year term from 2026 to 2031
- Maximum salary for the Whole Time Director capped at ₹1,00,00,000 (₹1 crore) per annum plus perquisites
- Cost Auditor remuneration for FY27 proposed at ₹4,00,000 plus applicable taxes
Gufic Biosciences has approved the re-appointment of Mr. Pankaj J Gandhi as Whole Time Director for a further five-year term, effective from September 07, 2026, to September 06, 2031. Mr. Gandhi possesses over 30 years of experience in regulatory liaison, a critical function as the company seeks to scale its Rs 360 Cr Indore facility and target USFDA approvals. The re-appointment is subject to shareholder approval at the upcoming 42nd Annual General Meeting. This move ensures leadership continuity in regulatory compliance during a phase where the company aims for 15-20% revenue growth.
- Re-appointment of Mr. Pankaj J Gandhi for a 5-year term starting September 07, 2026.
- Mr. Gandhi brings over 30 years of experience in pharmaceutical regulatory liaison and compliance.
- The appointment is subject to shareholder approval at the 42nd Annual General Meeting.
- Board meeting for the approval lasted 1 hour and 55 minutes, concluding at 06:25 p.m. on July 31, 2026.
Financial Performance
Revenue Growth by Segment
Infertility division is a key growth driver; Critical Care and Sparsh divisions grew 8-10% in volume, though value growth was limited to 4-6% due to API price erosion. CMO business declined in H1 FY26 as capacity was prioritized for higher-margin exports.
Geographic Revenue Split
International business currently contributes 20-25% of total revenue, with management targeting an increase to 30-35% to drive gross margin expansion. Domestic business remains the primary contributor at approximately 75-80%.
Profitability Margins
Gross margins improved in Q2 FY26 due to a better sales mix and increased international business. PAT margin improved to 6.47% in Q2 FY26 from 5.32% in Q1 FY26. Operating margins are expected to remain stable above 15% over the medium term.
EBITDA Margin
EBITDA margin stood at 16.45% in Q2 FY26 (INR 37.9 Cr), up 182 bps from 14.63% in Q1 FY26 (INR 33.2 Cr). The improvement is attributed to higher-margin international sales and better absorption of fixed costs as the Indore plant scales.
Capital Expenditure
The company recently completed a major capex of INR 360 Cr for the Indore plant which commenced operations in early 2025. Future maintenance capex is projected at INR 15-20 Cr for the next 12 months.
Credit Rating & Borrowing
Long-term rating of [ICRA]A- (Stable) and Short-term rating of [ICRA]A2+. Interest coverage ratio was robust at 5.7 times in FY25. Average fund-based limit utilization is approximately 57-78%.
Operational Drivers
Raw Materials
Active Pharmaceutical Ingredients (APIs) represent the primary raw material cost. Specific API names are not listed, but they are subject to price volatility which is passed through in CMO contracts.
Import Sources
A significant portion of raw materials is imported to support the formulations business, though specific countries are not detailed in the provided documents.
Key Suppliers
Not specifically named in the documents; however, the company maintains healthy relationships with a broad base of suppliers to mitigate procurement risks.
Capacity Expansion
Indore plant is currently at 25% production capacity and 23% sales utilization as of Q2 FY26. Navsari plant is operating at 100% utilization. The Indore plant is designed to meet USFDA standards to support future export growth.
Raw Material Costs
Raw material costs are susceptible to global price fluctuations; however, a downward trend in API prices recently led to price reductions for end-customers in the Critical Care segment to maintain market share.
Manufacturing Efficiency
Focus is shifting from CMO to own-branded products and exports to maximize returns on the INR 360 Cr Indore investment. Indore is currently scaling up with 40 molecules already transferred.
Logistics & Distribution
Distribution is managed through a hybrid model; the company recently reverted to a primary billing model (selling to stockists) to reduce working capital intensity from the previous direct-to-hospital model.
Strategic Growth
Expected Growth Rate
15-20%
Growth Strategy
Growth will be driven by the ramp-up of the Indore facility, increasing the share of international business to 30-35%, and launching new products like Semaglutide (GLP-1) in partnership with Hetero. The company is also expanding into regulated markets like Canada, South Africa, and Brazil.
Products & Services
Lyophilised injectables, infertility hormones, Critical Care medicines, Sparsh division products, and aesthetic products like Botox.
Brand Portfolio
Stunnox (Botox), Puregraf, Guficin Alpa, Supergraf (Infertility), and various hospital-first injectable platforms.
New Products/Services
Launch of Semaglutide (GLP-1) as a CMO for Hetero expected in Q1 FY27 following patent expiry in March 2026. Continued expansion of the Botox (Stunnox) portfolio.
Market Expansion
Targeting regulated and semi-regulated international markets including the US (pending FDA approval), Canada, South Africa, and Brazil.
Strategic Alliances
Strategic CMO partnership with Hetero for Remdesivir and Semaglutide (GLP-1).
External Factors
Industry Trends
The industry is shifting toward specialized delivery systems like lyophilization. Gufic is positioning itself as a leader in this niche with its new Indore plant, moving away from low-margin CMO work toward high-value branded exports.
Competitive Landscape
Intense competition from both large multinational pharmaceutical companies and established domestic players like Zydus and Lupin.
Competitive Moat
Moat is built on specialized manufacturing capabilities in lyophilised injectables and a strong hospital-first distribution network. Sustainability depends on maintaining high quality standards and securing international regulatory approvals.
Macro Economic Sensitivity
The pharmaceutical industry is relatively resilient to GDP fluctuations but sensitive to healthcare policy changes and government spending.
Consumer Behavior
Increasing demand for aesthetic treatments (Botox) and infertility treatments is driving growth in the company's specialized divisions.
Geopolitical Risks
Trade barriers or regulatory changes in target export markets (Brazil, South Africa) could impact the international expansion strategy.
Regulatory & Governance
Industry Regulations
Operations are highly regulated by state and central agencies (CDSCO) regarding drug pricing (DPCO), manufacturing standards (GMP), and clinical trials.
Environmental Compliance
The company conducts regular training and awareness programs to ensure compliance with environmental and social requirements inherent in pharma manufacturing.
Taxation Policy Impact
The company noted a steep increase in current tax effects in Q2 FY26, partly related to cash management and timing of payments.
Risk Analysis
Key Uncertainties
The primary uncertainty is the timeline for receiving international regulatory approvals (e.g., USFDA) for the Indore plant, which is critical for achieving the 15-20% growth target.
Geographic Concentration Risk
Heavy reliance on the Indian domestic market (approx. 75-80% of revenue), though international diversification is underway.
Third Party Dependencies
Dependency on CMO partners like Hetero for specific high-growth molecules like Semaglutide.
Technology Obsolescence Risk
Risk is mitigated by the recent INR 360 Cr investment in state-of-the-art lyophilization technology at the Indore facility.
Credit & Counterparty Risk
Receivable days are high at 144-150 days, reflecting the credit periods offered to hospital and institutional clients.