BSECompany Update1d ago · 14 Nov 2026, 08:34 pm
Investor Presentation is attached herewith
Gufic Biosciences Ltd · 509079
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Gufic Biosciences Ltd has released an investor presentation for Q2 FY2027, highlighting its business and financial updates. The company has made progress in its manufacturing platform, hospital injectable platform, women's health platform, and botulinum toxin platform. It has also expanded its international business and research and development efforts. The presentation provides a detailed overview of the company's performance and future prospects.
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Governance Concern2/10
Regulatory Risk3/10
Balance Sheet Risk5/10
Liquidity Impact8/10
Market Sentiment6/10
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Gufic Biosciences Ltd - 509079 - Announcement under Regulation 30 (LODR)-Investor Presentation
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348/LG/SE/NOV/2026/GBSL
November 14, 2026
To, To,
BSE Limited National Stock Exchange of India Limited
Phiroze Jeejeebhoy Towers, Exchange Plaza, Bandra Kurla Complex,
Dalal Street, Fort, Mumbai – 400 001 Bandra (E), Mumbai – 400 051
Scrip Code: 509079 Scrip Symbol: GUFICBIO
Subject: Investor Presentation
Dear Sir/Madam,
Pursuant to Regulation 30 of Securities and Exchange Board of India (Listing Obligations and
Disclosure Requirements) Regulations, 2015, please find enclosed herewith the Investor
Presentation on Unaudited Financial Results of the Company for the quarter and half year
ended September 30, 2026.
Kindly take the same on record.
Thanking You,
Yours truly,
For Gufic Biosciences Limited
Ami Shah
Company Secretary & Compliance Officer
Membership No. A39579
Encl.: As above
INVESTOR PRESENTATION
Delivering Care &
Cure
Q2 FY2027
Gufic Biosciences Limited
IMPORTANT NOTICE
Safe Harbor
This presentation has been prepared by and is the sole responsibility of Gufic Biosciences Certain statements contained in this presentation that are not statements of historical fact
Limited (the “Company”). By accessing this presentation, you are agreeing to be bound by constitute “forward-looking statements.” You can generally identify forward looking
the trailing restrictions. statements by terminology such as “aim”, “anticipate”, “believe”, “continue”, “could”,
“estimate”, “expect”, “intend”, “may”, “objective”, “goal”, “plan”, “potential”, “project”,
This presentation does not constitute or form part of any offer or invitation or inducement
“pursue”, “shall”, “should”, “will”, “would”, or other words or phrases of similar import.
to sell or issue, or any solicitation of any offer or recommendation to purchase or
These forward-looking statements involve known and unknown risks, uncertainties,
subscribe for, any securities of the Company, nor shall it or any part of it or the fact of its
assumptions and other factors that may cause the Company’s actual results, performance
distribution form the basis of, or be relied on in connection with, any contract or
or achievements to be materially different from any future results, performance or
commitment thereof. In particular, this presentation is not intended to be a prospectus or
achievements expressed or implied by such forward-looking statements or other
offer document under the applicable laws of any jurisdiction, including India. No
projections. Important factors that could cause actual results, performance or
representation or warranty, express or implied, is made as to, and no reliance should be
achievements to differ materially include, among others: (a) our ability to successfully
placed on, the fairness, accuracy, completeness or correctness of the information or
implement our strategy, (b) our growth and expansion plans, (c) changes in regulatory
opinions contained in this presentation. Such information and opinions are in all events
norms applicable to the Company, (d) technological changes, (e) investment income, (f)
not current after the date of this presentation. There is no obligation to update, modify or
cash flow projections, and (g) other risks.
amend this communication or to otherwise notify the recipient if the information, opinion,
projection, forecast or estimate set forth herein, changes or subsequently becomes This presentation is for general information purposes only, without regard to any specific
inaccurate. objectives, financial situations or informational needs of any particular person. The
Company may alter, modify or otherwise change in any manner the content of this
presentation, without obligation to notify any person of such change or changes.
Gufic Biosciences Limited | Investor Presentation Q2 FY2027 2
Q2 FY27 Business & Financial
Highlights
• Indore facility: the manufacturing platform
• Hospital injectable platform
• Women's health platform
• Botulinum toxin platform
• Nutra, Ayurveda & others
• International business and Indore scale-up
• Research & development
• Financials
Q2 FY27 BUSINESS UPDATE
Q2 FY27 at a glance: direction across the business
1 Indore manufacturing platform 2 Hospital injectable platform 3 Women's health platform
The US FDA inspection brings the regulated- Formulary depth ahead of portfolio breadth, In fertility, evidence and depth of clinic wallet
market timeline forward. Scale-up stays own-manufactured brands and differentiated share rather than centre count; in Zenova, a
deliberately paced; the operating leverage sits delivery formats as the point of difference, and prescription-led portfolio in which power brands
behind closing the observations and the new account-acquisition models on a clean and several growth engines now carry the
certifications in progress. receivable base. division.
4 Botulinum toxin platform 5 Nutra, Ayurveda & others 6 International business
Aesthetics moves from a single toxin brand A science-led chronic care platform built on a Registrations this quarter converted directly into
towards a full portfolio as fillers arrives, backed leading herbal franchise —the core holding first orders in the Gulf and Latin America, while
by Indian clinical evidence; therapeutics leadership, newer pillars gaining weight, and the the European footprint widened through Gufic
continues to compound quietly on protocol- allopathic pain adjacency now commercial. Ireland and partners —approvals now
mandated demand. translating into supply rather than sitting on file.
Gufic Biosciences Limited | Investor Presentation Q2 FY2027 4
Q2 FY27 BUSINESS UPDATE | MANUFACTURING
Indore facility: the manufacturing platform
We have built one of the most advanced lyophilized Q2 FY27 PROGRESS
injectable facilities, commenced production in October
Regulated-market readiness
2024
Q2 work moved from capability extension to regulated-market readiness. The
site is now registered with the US FDA, a first product dossier was filed from it,
DESIGNED TO GLOBAL REGULATORY STANDARDS
and audits by prospective partners for the US and UK markets were hosted.
WHO GMP EU GMP ANVISA MHRA USFDA
INSTALLED CAPACITY Capability extension
The depot suite is ready for trials and media fills ahead of domestic commercial
50 mn 30 mn 72 mn
batches. The spray-dried route for a lipid-based antifungal is on the verge of
completion, and an injectable emulsion format moved through scale-up, with
Lyophilized vials per Liquid vials per year Ampoules per year
exhibit batches planned in Q3.
year
Commercial production commenced in October 2024.
The US FDA inspection brings the regulated-market timeline forward. Scale-up stays deliberately paced; the operating leverage sits behind closing the observations
DIRECTION
and the certifications in progress.
Gufic Biosciences Limited | Investor Presentation Q2 FY2027 5
Q2 FY27 BUSINESS UPDATE | MANUFACTURING
Indore facility: timeline of our phased approach
Milestone Target Status Commentary
Installation & Operational Qualification Completed –facility meets WHO GMP, EU GMP, ANVISA, MHRA, USFDA design
October 2023 ●Completed
(IQ/OQ) standards
Performance Qualification (PQ) All Lines &
Dec 2023 –Jun 2024 ●Completed Completed with multiple container trials; parameters locked
Utilities
Media Fills (Aseptic Process Simulations) Jul 2024 –Oct 2024 ●Completed Completed for all four lines; sterility validated
Product Permissions from State FDA Ongoing ●In progress 203 approvals received to date; more in pipeline
Tech Transfer for existing products from
Completed for 40 products; stability studies in progress. 27 more products under
Navsari & Process Validation Batches for Oct 2024 –ongoing ●In progress
development
initial products
Vendor Audits Indian Pharma Majors H1-FY26 ●In progress 20+ completed, more lined up; CMO contracts commenced
30% Capacity Utilization FY26 ●In progress On-track
Global Regulatory Clearance
EU GMP & UK MHRA FY27 ●In progress EU audit completed; compliance report submitted; certification awaited
Pre-approval inspection completed; three o
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