SYNGENENSE9 September 2025

Syngene International Limited has informed the Exchange about Investor Presentation

Syngene International Limited

Ref: Syn/CS/SE/IP/2025-26/Sept/05

September 09, 2025

To, The Manager, BSE Limited Corporate Relationship Department Dalal Street, Mumbai – 400 001 Scrip Code: 539268

Dear Sir/Madam,

Sub: Investor Presentation

Syngene International Limited Biocon SEZ, Biocon Park, Plot No. 2 & 3, Bommasandra Industrial Area, IV Phase, Jigani Link Road, Bengaluru 560099, Karnataka, India. T +91 80 6891 8000 F +91 80 6891 8808 CIN: L85110KA1993PLC014937 www.syngeneintl.com

To, The Manager, National Stock Exchange of India Limited Corporate Communication Department Bandra (EAST), Mumbai – 400 051 Scrip Symbol: SYNGENE

In continuation of our earlier intimation vide reference no. Ref: Syn/CS/SE/Reg 30/2025-26/Sept/03 dated September 04, 2025 and in accordance with Regulation 30 of the SEBI (Listing Obligations and Disclosure Requirements) Regulations, 2015, please find enclosed the presentation that we will be sharing with the Investors and Analysts at the meeting scheduled today, i.e., September 09, 2025.

Kindly note that no additional information will be disclosed to Analysts or Investors other than the information presented earlier and already available in the public domain.

The above-mentioned Investor Presentation will also be available on the website of the Company www.syngeneintl.com.

This is for your information and records.

Thanking You,

Yours faithfully,

For SYNGENE INTERNATIONAL LIMITED

_____________ Chethan Yogesh Company Secretary & Compliance Officer

Enclosed: Investor Presentation.

Phase,

B o m m a s a n d r a I n d u s t r i a l A r e a , I V

B o m m a s a n d r a I

Unit-3 plant visit for Investors – 9th September 2025

Agenda

Sr. no

Timing

Particulars

Led by

I

11:30 AM – 12:15 PM Tea + Brief Introduction (PPT) of the facility

II

12:15 PM- 1:30 PM

Divide participant in 2 groups

Visit to Drug Substance unit+ utility and facility round area for each group

Deepak Jain (CFO)

Himanshu Saxena (Head, Biologics manufacturing)

Himanshu Saxena ( Head, Biologics manufacturing)

Mr. Nainesh Dwivedi (Head, Quality for Unit-3)

Mr. Dhaval Trivedi (Head, Program Management, Biologics)

Mr. Ram Sarma (DP, Manufacturing plant head)

Mr. Satish M (DS Manufacturing plant Head)

Mr. Babu V (Engineering & maintenance, Unit-3)

III

IV

1:45 PM- 2:30 PM

Lunch / Buffer Time

2:45 PM- 3:45 PM

Feedback by Investors

Peter Bains (CEO) to join virtually

Interaction / Q&A with CFO / CEO

Deepak Jain (CFO)

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2

Syngene Management & Leadership for Unit-3 visit

Peter Bains Managing Director & CEO

Deepak Jain Chief Financial Officer

Himanshu Saxena Head, Biologics Manufacturing

• MD & CEO, Syngene International with over

3 decades of experience the pharmaceutical and biotechnology sectors

• Rejoined Syngene in Feb 2025 post spearheading

Syngene’s IPO in FY16

• Prior to joining Syngene International, Peter served

as Group CEO for Biocon

• CFO, Syngene International with over 25 years

• Over two decades of expertise in supply chain

of experience

Joined Syngene in September 2024, Appointed as CFO on Dec 01,2024

• Oversees the finance, supply chain, legal,

secretarial and plays an important role in driving strategy, and enabling organizational growth

management, business strategy, and pharmaceutical manufacturing

• Currently serving as Head, Biologics

manufacturing. Joined Syngene in January,2024

• Previous work experience with Cadila and Astra

Zeneca Pharma India Ltd

• Previously worked as CEO and was on the Board of Syngene for almost six years starting 2010 and led the company to its successful public listing in 2015

• Previous experience as CFO, Ather energy. Prior to that, served as India CFO for First Advantage and for Apple

• Also Served as CEO, Sosei Group, a Japanese listed

biopharmaceutical company

• Held various leadership roles at Procter & Gamble, and Ernst & Young India

• Worked in various Leadership roles for

GlaxoSmithKline over a period of 23 years

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3

01

Introduction and overview of facility

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Background – acquired multimodal biologics facility from Stelis Biopharma with integrated drug substance and commercial DP capability in Dec 2023

Why we acquired

Immediate capacity addition Syngene’s existing capacity was fully utilized post signing 10 year agreement with Zoetis in FY23. Unit-3 added immediate capacity (20 KL of biologics drug substance capacity) with potential for future expansion up to a further 20 KL

Capability enhancement Facility includes commercial scale, high speed, fill-finish unit – an essential capability for drug product manufacturing

Added drug substance capacity and drug product capability years earlier than our internal capex program

Operational Synergy Facility is located near to Biocon park which houses Syngene’s Biologics labs & other facilities enabling shared leadership and essential functions

250

200

150

100

50

0

Strengthens Syngene’s position in the fastest growing segment of the global CRDMO market

Market size* (USD bn)

8% CAGR

144

22

99

23

2023

213

39

137

37

2028

Value Buy State of the art facility acquired at Rs 617 Crores (USD 75 Mn) fully funded through internal accruals and cash

CRO

SM CDMO

LM CDMO

Overall CRDMO

Source : Frost & Sullivan: Iindependent Market Assessment of the Global and Indian CRDMO Market * Market size does not include Clinical CRO market

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5

Guidance given at time of acquisition. We are maintaining the guidance for now

Asset turnover of 1x in less than 5 years

$75m acquisition price (Acquisition concluded at gross value of Rs 617 crores. Value buy as company recorded Capital reserve due to purchase price < fair value of facility)

$10m modification capex (INR 100 Crores to repurpose and revalidate the facility)

$85m to operationalise

Operating Margin

Minor dilution of operating margins in short term as a result of costs to be incurred in this facility

EBITDA margins expected to be in line with the Company average from FY29

Contribution to PAT

Plant to positively contribute to the bottom line from FY27

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Current update and strategic focus - the facility was part capitalized in Q1 FY26. Focus is to drive integrated projects across human and animal health

Where are we now

Strategic focus

Received local regulatory approvals in May 2025

Focus on building pipeline across human health and animal health

Part of Unit-3 facility became operational in Q1 FY26

• 1 out 2 line in DS (8 KL 4*2 KL commissioned)

Doing Clinical projects ; delivered a GMP clinical batch of drug substance for a US based client in Q1 FY26

Seeing good client traction and response across human and animal health

Integrated clinical manufacturing projects (Both Animal & Human health) and commercial/late-stage manufacturing of mAbs over time along with drug product capabilities

Innovation for cost efficiency : Reducing cost per gram through process innovation

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7

Bird’s Eye View of Syngene Unit-3

Salient features of the multi modal facility comprising end to end DS and DP manufacturing capability

• Drug Substance (DS) :

• 8 KL (4*2 KL) commissioned

• Feasibility for perfusion

• Drug Product (DP) :

• Commercial scale, high speed, fill-finish unit

• 2 integrated vials lines: 520 vials/min

• 250 million vials annual capacity at 2 mL fill volume

• 2-100 mL fill volume feasibility

• 2 new isolator lines (100 & 600 vials/min) available for installation

• Clinical Manufacturing : 200L/500L/2000L depending on client requirement

• Quality Control (QC) : Fully equipped Lab for product quality testing

• Warehouse : Large warehouse for accommodating raw materials &

consumables

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Integration Journey: Acquisition to Operation in 7 Months

Production

Equipment Qualification and Area Qualification

Feb-June 2024

Equipment Qualification

July 2024

15th July test batch initiated with qualified facility and equipment, completed successfully with desired outcome.

Computer System Validation

Environmental monitoring and area qualification

Facility Modification

Acquisition

1st Dec 2023 Acquisition completed

Jan-May 2024

Infrastructure

modification

Operations

Q1 FY26

Part of Unit-3 facility became operational in Q1 FY26

Delivered a GMP clinical batch of drug substance for a US based client

Consistent Facility Performance

Multiple batches successfully executed with no facility-related issues.

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9

Unit – 3 (SU3) Site Master Plan

ETP

Block-3 200L DS,DP, QC

Utility Block -2

Block-2 2,000L DS + 2,000L DS Expansion

Utility Block -1

Entry to the site

Safety Assembly Point

Area Details

Plot area

22,000 m2 (5.4 Acres)

Block Name

Block 1

Expansion Area available

Block 2 - DS Block

2 Floors (Ground Floor+ First Floor) First floor (2 wings of 10 KL capacity each) – one DS wing operational now with 8 KL (4*2 KL commissioned)

Block 3

Clinical DS (200L), 2 DP vial lines, QC, Admin

Utility Block 1

Steam, Generator

Utility Block 2

WFI (Water for Injection)

Facilities to be visited today

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10

02

Site visit to DS / Utilities

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Site visit – protocols

• Clothing: Minimum Gowning, Head cap & Shoe cover

• Decorum to be maintained while visiting labs

• Please limit Q&A with the technical teams related to

infrastructure, technical/plant details etc.

• We will have a separate Q&A/feedback session with Peter

and Deepak to cover strategic/financial aspects

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12 12

03

Lunch

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04

Feedback/Q&A

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Feedback/ Q&A

Feedback/thoughts on the site, capabilities, infrastructure from investors

• Open Q&A

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Thank you

© 2025 Syngene International Limited, Bengaluru, India. All Rights Reserved. Syngene believes the information in this document is accurate as of its publication date; such information is subject to change without notice. Syngene acknowledges the proprietary rights of other companies to the trademarks, product names and such other intellectual property rights mentioned in this document. Except as expressly permitted, neither this documentation nor any part of it may be reproduced, stored in a retrieval system, or transmitted in any form or by any means, electronic, mechanical, printing, photocopying, recording or otherwise, without the prior permission of Syngene International Limited and/ or any named intellectual property rights holders under this document.

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