NSEGeneral Updates19 Jun 2026 · 19 Jun 2026, 01:02 am
General Updates
Jubilant Pharmova Limited · JUBLPHARMA
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Jubilant Pharmova Limited has announced the completion of a USFDA inspection at its Jubilant HollisterStier LLC (JHS) contract manufacturing facility in Spokane, Washington, USA. The inspection of the CMO business concluded on June 17, 2026. While the company confirmed the inspection's completion, it has not yet disclosed the specific outcome, such as any observations or regulatory actions. This update signifies a key regulatory milestone for its US operations, with investors awaiting further details on the inspection's findings.
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Jubilant Pharmova Limited has informed the Exchange about General Updates
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JUBLPHARMA_19062026010202_Exchange_Intimation_USFDA_June_2026F.pdf
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June 19, 2026
BSE Limited The National Stock Exchange of India Limited
Floor 25, P. J. Towers Exchange Plaza
Dalal Street, Bandra Kurla Complex, Bandra (E)
Mumbai - 400 001 Mumbai - 400 051
Scrip Code: 530019 Symbol: JUBLPHARMA
Subject: Completion of USFDA Inspection
Dear Sirs,
The USFDA has completed an inspection of the Jubilant HollisterStier LLC (“JHS”) CMO business at
Spokane WA, U.S.A facility. We are enclosing the details regarding the dates of the inspection and
outcome of the inspection in accordance with Regulation 30 of the Securities and Exchange Board of
India (Listing Obligations and Disclosure Requirements) Regulations, 2015.
Date and Time of receipt - June 17, 2026, 15:30 PM (PST) i.e. June 18, 2026, 04:00 AM (IST).
We request you to take the same on record.
Thanking you,
Yours faithfully,
For Jubilant Pharmova Limited
Naresh Kapoor
Company Secretary
Encl: As above
Jubilant Pharmova announces completion of USFDA inspection of
Contract manufacturing facility at Spokane WA. U.S.A
Noida, June 18, 2026: Jubilant Pharmova Limited (“Company”) today announced that United States
Food and Drug Administration (USFDA) has concluded an inspection of Jubilant HollisterStier LLC
(JHS)’s contract manufacturing facility located in Spokane, WA. U.S.A on June 17, 2026. The USFDA
had issued eight (8) observations, none of which are related to sterility assurance concerns.
JHS will respond to the inspection observations within 15 business days. The Company is committed
to addressing the observations comprehensively.
Jubilant HollisterStier LLC is a subsidiary of Jubilant Pharma Holding Inc., which is a subsidiary of
Jubilant Pharma Limited, Singapore, a wholly owned subsidiary of the company.
About Jubilant HollisterStier LLC
Jubilant HollisterStier is a leading integrated contract manufacturer of sterile injectables (both liquid
and lyophilization) and ophthalmics (Ointment, liquid and creams). With facilities in North America,
Jubilant HollisterStier provides specialized manufacturing for the pharmaceutical and
biopharmaceutical industries. The services include a full range of support to streamline the
manufacturing processes, from process qualifications through commercial release.
About Jubilant Pharma Limited
Jubilant Pharma Limited (JPL), a Company incorporated under the laws of Singapore and a wholly-
owned subsidiary of Jubilant Pharmova Limited, is an integrated global pharmaceutical company
engaged in manufacturing and supply of Radiopharmaceuticals with a network of 45 radio-pharmacies
in the US, Allergy Immunotherapy, Contract Manufacturing of Sterile Injectables and Non-sterile
products and Solid Dosage Formulations through multiple manufacturing facilities that cater to all the
regulated market including USA, Europe and other geographies. The Company has a team of around
3,200 multicultural people across the globe and is committed to delivering value to its customers
spread across over 75 countries. It is well recognized as a 'Partner of Choice' by leading pharmaceutical
companies globally.
About Jubilant Pharmova Limited
Jubilant Pharmova Limited is an integrated global pharmaceutical company engaged in Radiopharma,
Allergy Immunotherapy, Contract Development and Manufacturing of sterile injectable, Contract
Research Development and Manufacturing, Generics and Proprietary Novel Drugs businesses. With a
network of 45 radiopharmacies in the USA, the Radiopharma business is engaged in manufacturing
and supply of radiopharmaceutical products and services. The Allergy Immunotherapy business is
involved in the manufacturing and supply of allergic extracts and venom products in the USA and other
markets such as Canada, Europe and Australia. Contract Development and Manufacturing of sterile
injectables, with facilities in Spokane, USA, and Montreal, Canada, delivers end-to-end manufacturing
solutions, including sterile fill-and-finish injectables (liquid and lyophilized), comprehensive
ophthalmic products (liquids, ointments and creams) and ampoules. Contract Research Development
and Manufacturing business provides end-to-end drug discovery and development services to the
pharmaceutical and biotech industries through three world class research centres (two in India and
one in France) and a US FDA approved, Active Pharmaceutical Ingredients manufacturing facility in
Nanjangud, Karnataka. The Generics business focuses on development, manufacturing and
distribution of Solid Dosage Formulations through multiple manufacturing facilities that cater to all
the regulated market including USA, Europe and other geographies. Proprietary Novel Drugs is an
innovative biopharmaceutical business developing breakthrough therapies in the area of oncology and
auto-immune disorders. Jubilant Pharmova has a team of around 5,500 multicultural people across
the globe. The Company is well recognised as a ‘Partner of Choice’ by leading pharmaceuticals
companies globally. For more information, please visit: www.jubilantpharmova.com.
For more information, please contact:
For Investors Siddharth Rangnekar
Pankaj Dhawan CDR India
Phone: +91 120 436 1105 Phone: +91 97699 19966
E-mail: Pankaj.dhawan@jubl.com E-mail: siddharth@cdr-india.com
For Media Jyoti Sharma
Sandipan Ghatak Ad Factors PR
Phone: +91-98107 76182 Phone: +91 9810519900
E-mail: sandipan.ghatak@jubl.com E-mail: jyoti.sharma@adfactorspr.com
Disclaimer
Statements in this document relating to future status, events, or circumstances, including but not limited to
statements about plans and objectives, the progress and results of research and development, potential product
characteristics and uses, product sales potential and target dates for product launch are forward-looking
statements based on estimates and the anticipated effects of future events on current and developing
circumstances. Such statements are subject to numerous risks and uncertainties and are not necessarily
predictive of future results. Actual results may differ materially from those anticipated in the forward-looking
statements. Jubilant Pharmova may, from time to time, make additional written and oral forward-looking
statements, including statements contained in the company’s filings with the regulatory bodies and its reports
to shareholders. The company assumes no obligation to update forward-looking statements to reflect actual
results, changed assumptions or other factors.