SENORESNSE16 May 2025

Senores Pharmaceuticals Limited has informed the Exchange about Investor Presentation

Senores Pharmaceuticals Limited

Date: May 16, 2025

To, Sr. General Manager Listing Department BSE Limited Phiroze Jeejeebhoy Towers Dalal Street Mumbai – 400 001

To, Sr. General Manager Listing Department National Stock Exchange of India Limited Exchange Plaza, C-1, Block G Bandra Kurla Complex Bandra (E), Mumbai – 400 051

BSE Scrip Code: 544319

NSE Symbol: SENORES

Sub.: Intimation under Regulations 30 of the Securities and Exchange Board of India (Listing Obligations and Disclosure Requirements) Regulations, 2015 ‐ Investor Presentation

Dear Sir/Madam,

In terms of Regulation 30 of Securities and Exchange Board of India (Listing Obligations and Disclosure Requirements) Regulations, 2015 and our intimation dated May 12, 2025 regarding the Earnings Conference Call, we enclose herewith the Investor Presentation for Q4 and FY25.

The aforesaid information is also being hosted on the Company's website at www.senorespharma.com.

You are requested to take the same on record.

Thanking you.

For Senores Pharmaceuticals Limited

Vinay Kumar Mishra Company Secretary and Compliance Officer ICSI Membership No.: F11464

Enclosures: As above

Senores Pharmaceuticals Limited  1101 to 1103, 11th Floor, South Tower, One42, Opp. Jayantilal Park,  Ambali Bopal Road, Ahmedabad‐380054, Gujarat, India

P: +91 79 2999 9857  |  E: info@senorespharma.com  W: www.senorespharma.com  |  CIN No.: L24290GJ2017PLC100263

Investor Presentation

May 2025

Safe Harbor

This presentation and the accompanying slides (the “Presentation”), which have been prepared by Senores Pharmaceuticals Limited (the “Company” / “SPL”), have been prepared

solely for information purposes and do not constitute any offer, recommendation or invitation to purchase or subscribe for any securities, and shall not form the basis or be relied

on in connection with any contract or binding commitment whatsoever. No offering of securities of the Company will be made except by means of a statutory offering document

containing detailed information about the Company.

This Presentation has been prepared by the Company based on information and data which the Company considers reliable, but the Company makes no representation or warranty, express or implied, whatsoever, and no reliance shall be placed on, the truth, accuracy, completeness, fairness and reasonableness of the contents of this Presentation.

This Presentation may not be all inclusive and may not contain all of the information that you may consider material. Any liability in respect of the contents of, or any omission

from, this Presentation is expressly excluded.

This presentation contains certain forward looking statements concerning the Company’s future business prospects and business profitability, which are subject to a number of

risks and uncertainties and the actual results could materially differ from those in such forward looking statements. The risks and uncertainties relating to these statements

include, but are not limited to, risks and uncertainties regarding fluctuations in earnings, our ability to manage growth, competition (both domestic and international), economic

growth in India and abroad, ability to attract and retain highly skilled professionals, time and cost over runs on contracts, our ability to manage our international operations,

government policies and actions regulations, interest and other fiscal costs generally prevailing in the economy. The Company does not undertake to make any announcement in

case any of these forward looking statements become materially incorrect in future or update any forward looking statements made from time to time by or on behalf of the

Company.

This Presentation contains data and statistics from certain reports and the F&S Report, which is subject to the following disclaimer Frost & Sullivan has taken due care and caution

in preparing this report (“Overview of the Global Pharma Market’' Report) based on the information obtained by Frost & Sullivan from sources which it considers reliable (“Data”).

This Report is not a recommendation to invest / disinvest in any entity covered in the Report and no part of this Report should be construed as an expert advice or investment advice or any form of investment banking within the meaning of any law or regulation. Without limiting the generality of the foregoing, nothing in the Report is to be construed as

Frost & Sullivan providing or intending to provide any services in jurisdictions where Frost & Sullivan does not have the necessary permission and/or registration to carry out its

business activities in this regard. Senores Pharmaceuticals Limited will be responsible for ensuring compliances and consequences of non-compliances for use of the (“Overview of the Global Pharma Market’') Report or part thereof outside India. No part of this Frost & Sullivan Report may be published/reproduced in any form without Frost & Sullivan’s prior

written approval.

2

Financial Highlights Q4 and FY25

Private & Confidential

Key Operational Highlights

Regulated Markets

22

28

Emerging Markets

285

Owned Commercial Products

Pipeline CGT Opportunity Products

Approved Products

61

22

636

Approved ANDA Products

CDMO/CMO Commercial Products

Products Under Registration

51

69

40+

Pipeline Products

CDMO/CMO Pipeline Products

Countries Present

4

Consolidated Financial Highlights – Q4 & FY25

Income up by 91%

Y-o-Y for FY25

EBIDTA up by 145%

Y-o-Y for FY25

PBT up by 183%

Y-o-Y for FY25

Income (INR Crs)*

EBITDA (INR Crs)

PBT (INR Crs)

89.2%

410.4

+131.7%

101.8

183.0%

70.6

17.3%

102.4

120.1

216.9

+13.3%

22.4

25.4

43.9

+17.5%

17.6

20.7

24.9

Q4FY24

Q4FY25

FY24

FY25

Q4FY24

Q4FY25

FY24

FY25

Q4FY24

Q4FY25

FY24

FY25

Gross Margin (%)

EBITDA Margin (%)

PBT Margin (%)

55.7%

52.2%

51.1%

56.0%

21.9%

21.1%

20.3%

24.8%

17.2%

17.2%

17.2%

11.5%

Q4FY24

Q4FY25

FY24

FY25

Q4FY24

Q4FY25

FY24

FY25

Q4FY24

Q4FY25

FY24

FY25

* Income includes Revenue from Operations and Other Operating Income. Note: FY24 includes financials of Ratnatris Pharmaceuticals from 14th December 2023 to 31st March 2024

5

Business Segment Financial Highlights – Q4 & FY25

) s r C R N

I ( e u n e v e R

Regulated Markets

Emerging Markets

Others

+68.7%

244.8

+174.1%

121.2

+17.4%

145.2

54.8

64.3

-2.7%

37.5

36.5

44.2

+76.2%

44.4

+90.1%

25.2

19.3

10.2

Q4 FY24

Q4 FY25

FY24

FY25

Q4 FY24

Q4 FY25

FY24

FY25

Q4 FY24

Q4 FY25

FY24

FY25

EBIDTA Margin for FY25 stood at 38%

EBIDTA Margin for FY25 stood at 7%

EBIDTA Margin for FY25 stood at 38%

)

%

( x i M e u n e v e R

Q4FY24

Q4FY25

9.9%

16.1%

FY24

11.7%

20.6%

FY25

10.8%

36.6%

53.5%

30.4%

53.5%

29.5%

59.7%

67.7%

Regulated Markets, contribute to 60% of total revenue for FY25 and will continue to remain the key focus market going forward.

Business model in the Emerging Markets is beginning to take shape. Share of Emerging markets has increased to ~30% for FY25 and this segment is expected to grow steadily from here on

Note: FY24 includes financials of Ratnatris Pharmaceuticals from 14th December 2023 to 31st March 2024.

6

Regulated Markets

Emerging Markets

Others

Management Commentary

Commenting on the Q4 & FY25 performance of the company Mr. Swapnil Shah, Managing Director for Senores Pharmaceuticals Limited said,

“We are pleased to report strong performance for FY25, driven by our strategy of developing niche products for Regulated Markets and expanding our CDMO/CMO operations. At the same time, we have continued to grow our presence and product portfolio in Emerging Markets. Our Total Income and Profit before Tax for FY25 have increased by 91% & 183% respectively on year-on-year basis, and we are optimistic about sustaining this momentum going forward.

Swapnil Shah Managing Director

We continued to make steady progress on our stated strategies. During the quarter, we expanded our portfolio in the Regulated Markets through acquisition of 14 ANDA’s from Dr. Reddy’s and 1 ANDA from Breckenridge Pharmaceuticals. A large part of this acquired ANDA basket has considerable government contract opportunities. Further, our CDMO/CMO segment is gaining traction and continued to scale up well. We have launched 1 new product in the CDMO/CMO segment during the quarter and have 69 products in pipeline.

Our shift in product portfolio and go-to-market strategies in the Emerging Markets business is beginning to give the desired results, which can be seen in the improvement in margin during the quarter. We have registered 48 new products across the Emerging Markets during Q4FY25, taking the total portfolio to 285 registered products.

Going forward, although the uncertainties due to the tariff situation in USA will have to be closely monitored, we believe we are well placed to navigate the same, given our USFDA-approved manufacturing facility in USA.

We will continue to focus on three key pillars going forward – Expansion of ANDA portfolio in Regulated Markets; Steady scale-up of CDMO/CMO segment in the Regulated Markets; and Portfolio expansion and profitability improvement in the Emerging Markets.”

7

Consolidated Profit & Loss Account – Q4 & FY25

Profit and Loss (INR Crs)

Revenue

Other Operating Income

Total Income

Total COGS

Gross Profit

Gross Margin (%)

Employee Cost

Other Expenses

EBITDA

EBITDA Margin (%)

Depreciation

Other Income

EBIT

Finance Cost

Profit before Tax

PBT Margin (%)

Tax + Minority Interest

Profit after Tax and Minority Interest

Profit after Tax and Minority Interest Margin (%)

EPS (INR)

Q4 FY25

Q4 FY24

108.7

11.5

120.2

57.5

62.7

52.2%

14.6

22.7

25.4

97.4

5.0

102.4

45.4

57.0

55.7%

18.2

16.4

22.4

21.1%

21.9%

5.2

5.8

26.0

5.3

20.7

17.2%

2.8

17.8

14.8%

3.8

3.7

2.0

20.6

3.0

17.6

17.2%

1.7

15.9

15.6%

8.0

YoY

11.6%

17.3%

9.9%

-350 bps

13.4%

-70 bps

25.9%

17.4%

0 bps

11.9%

-70 bps

FY25

390.8

19.5

410.4

180.7

229.7

56.0%

60.4

67.5

101.8

24.8%

16.8

7.2

92.1

21.6

70.6

17.2%

12.0

58.6

14.3%

16.1

FY24*

209.0

7.9

216.9

106.1

110.7

51.1%

35.5

31.3

43.9

19.4%

10.0

0.5

34.4

9.4

24.9

11.5%

-7.8

32.7

15.1%

12.2

YoY

87.0%

89.2%

107.4%

490 bps

131.7%

450 bps

167.9%

183.0%

570 bps

79.1%

-80 bps

*FY24 includes financials of Ratnatris Pharmaceuticals from 14th December 2023 to 31st March 2024

8

Other Financial Highlights – Q4 & FY25

Particulars (Rs Crs)

A: Other Operating Income

Product related service Income

Miscellaneous - Other Operating Income

Gain on Foreign Exchange Fluctuation (Net)

Total Other Operating Income

B: Interest Income

Total Other Income

Capex Plans:

Capex Incurred during FY 2025

Capex planned for next year

Q4FY25

Q4FY24

FY25

FY24

4.91

7.24

-0.67

11.48

5.82

17.30

3.78

2.03

0.89

6.70

0.28

6.98

7.68

7.94

3.92

19.54

7.15

26.69

4.13

2.72

1.07

7.92

0.46

8.38

In Cr

157.5

251.0

Working Capital Days

FY25

FY24

Inventory

43

69

Trade Receivables

108

228

Trade Payables

182

435

*FY24 includes financials of Ratnatris Pharmaceuticals from 14th December 2023 to 31st March 2024

9

Consolidated Balance Sheet

ASSETS (INR Crs) Non-Current Assets Property, Plant and Equipment Capital Work-in-Progress Goodwill Intangible Assets Right of Use Assets Intangible Assets under Development Non-Current Financial Assets Deferred Tax Assets (Net) Other Non-Current Assets Total Non-Current Assets

Current Assets Inventories Trade Receivables Cash & Cash Equivalents Bank Balances Other Than Cash & Cash Equivalents Loans Other Current Financial Assets Other current assets Total Current Assets

Mar-25 Mar-24

198.9 44.2 38.2 54.3 9.4 128.3 5.2 18.7 7.4 504.4

56.6 123.9 105.4 280.1 0.0 117.0 39.5 722.4

152.2 17.8 38.2 35.9 9.1 79.3 20.5 15.0 3.0 371.0

37.4 112.0 7.7 5.4 0.3 66.2 22.0 250.9

EQUITY AND LIABILITIES (INR Crs) Equity Equity Share Capital Other Equity Total Shareholder’s Fund Non-Controlling Interest Total Equity

Non-Current Liabilities Borrowings Lease Liabilities Provisions Total Non-Current Liabilities

Current Liabilities Borrowings Lease Liabilities Trade Payables Other Current Liabilities Other Current Financial Liabilities Provisions Current Tax Liabilities (net) Total Current Liabilities

Mar-25 Mar-24

46.1 740.1 786.2 26.1 812.2

162.5 8.2 3.3 173.9

142.3 1.8 67.2 6.0 7.8 2.1 13.5 240.7

30.5 173.8 204.3 27.4 231.7

133.7 7.8 1.2 142.7

114.7 1.5 113.0 5.2 4.6 1.4 7.1 247.5

Total ASSETS

1,226.9

621.9

Total EQUITY AND LIABILITIES

1,226.9

621.9

10

Consolidated Abridged Cash Flow Statement

Cash Flow Statement (INR Mn)

Profit/(Loss) Before Tax

Adjustments for Non-Cash and Non-Operational Expenses / (Incomes)

Operating Profit / (Loss) Before Working Capital Changes

Changes in Working Capital

Cash from Operations

Income Tax (Paid) / Refunded

Net Cash Flow from Operating Activities (A)

Net Cash Flow from Investing Activities (B)

Net Cash Flow from Financing Activities (C)

Net Change in Cash & Cash Equivalents during the Year (A+B+C)

Cash & Cash Equivalents at the Beginning of the Period

Cash & Cash Equivalents at the End of the Period

FY25

70.6

27.1

97.7

-134.4

-36.7

-9.2

-45.9

-429.5

573.1

97.7

7.6

105.4

FY24

24.9

17.9

42.8

-66.1

-23.2

-2.5

-25.7

-54.2

87.0

7.0

0.1

7.6

Note: FY24 includes financials of Ratnatris Pharmaceuticals from 14th December 2023 to 31st March 2024

11

Update on Utilization of Funds from IPO

Sr. No

Object as per Offer Document

Amount as proposed in the Offer Document

Amount utilized as on March 31, 2025

Amount Unutilized as on March 31, 2025

Remarks

1

2

3

4

5

6

7

Investment in one of our Subsidiaries, Havix, to fund capital expenditure requirements for setting up a manufacturing facility for the production of sterile injections in our Atlanta Facility

Re-payment/pre-payment, in full or in part, of certain borrowings availed by our Company

Investment in our Subsidiary, namely, Havix, for re- payment/pre-payment in full or in part, of certain borrowings availed by such Subsidiaries

Funding the working capital requirements of our Company

Investment in our Subsidiaries, namely Senores Pharmaceuticals Inc. and Ratnatris to fund their working capital requirements

Funding inorganic growth through acquisition and other strategic initiatives and general corporate purposes

Offer expenses

Total

107.0

73.5

20.2

43.3

59.5

154.4

42.2

500.0

-

43.6

3.9

20.2

22.4

35.7

31.0

156.8

107.0

29.9

16.3

23.1

37.1

118.7

11.2

343.3

Out of the unutilized amount Rs 130 crores parked as Fixed Deposit with HDFC Bank, Rs 209 crores parked as Fixed Deposit with ICICI Bank and balance held in HDFC bank account

12

About Senores Pharmaceuticals Limited

Private & Confidential

Introduction to Senores Pharma

Brief Overview Global Research driven Formulation Focused company engaged in developing & manufacturing of pharmaceutical products predominantly for the Regulated Markets of the US, Canada & UK across various therapeutic areas

At a Glance

Niche Product Identification Company focusses on identification, development and commercialization of products

R&D Capabilities Identification, development & manufacturing of diverse range of specialty, underpenetrated & complex pharmaceutical products across therapeutic areas & dosage forms

Regulated Market Approved Facility 1 USFDA & DEA approved formulation facility in the US

Partnerships

Partnerships with leading pharmaceutical companies across Regulated as well as Emerging Markets

Regulated Markets

Emerging Markets

14

Business Segments

59.7%

29.5%

10.8%

FY25 Income

INR 410 Crs

Regulated Markets

Emerging Markets

Others (API + Injectables + Other Op. Income

Regulated Markets Business

Emerging Markets Business

Primarily serves the US, Canada and United Kingdom

USFDA approved facility in Atlanta, US

Develop & manufacture pharmaceutical products for the Emerging Markets

W H O - GMP approved facility at Chhatral

22 Commercialized Products

61 Approved ANDA Products

51 Pipeline Products

28 Pipeline CG T Opportunity Products

Present in 40+ Countries

Approval for manufacturing facility from regulatory bodies of 10 countries

Product registration for 285 Products

Product applications filed for 636 Products

API Business

Critical Care Injectables Business

Manufacture APIs and caters to the domestic market and SAARC countries

Supply of critical care injectables across India to various hospitals through the distributors

Naroda facility compliant with Indian GMP

Field presence with 47 employees

Commercialized 16 APIs

Launched 56 Products

15

Key Events & Milestones

Incorporated as “Senores Pharmaceuticals Pvt. Ltd.” in India.

Incorporated a wholly owned subsidiary, Senores Pharmaceuticals Inc in the US

Consolidated presence in emerging markets by acquiring shares in Ratnatris Pharmaceuticals Pvt. Ltd.

Commenced manufacturing activities at its greenfield API plant located at Gujarat

2017

202 1 2021

2021

2023

2023

2024

2025

Entered into a new segment of API with acquisition of Ratnagene Lifescience Pvt. Ltd.1

Acquired majority stake in Havix, enhancing the ability to serve Regulated Markets through USFDA approved facility in US

Successful Listing on Stock Exchanges in India on BSE & NSE

Note: 1: Now merged with Senores Pharmaceuticals Limited with the appointed date being January 1, 2024

16

Key Strengths

Private & Confidential

Key Strengths of the Company

1 Distinct specialty and complex product portfolio built in a short span for Regulated

Markets

2 Long-term marketing arrangements with pharmaceutical companies in the Regulated

Markets

3 Presence in the Emerging Markets with portfolio, including specialty and complex

products

4 Strong R&D capabilities driving differentiated portfolio of products

5 US FDA approved facility in the US catering to the Regulated & Semi-Regulated Markets and WHO-GMP compliant facility in India catering to Emerging Markets

6 Professional & dedicated management teams for the diverse business verticals

18

1

Distinct Specialty & Complex Product Portfolio Built in a Short Span for Regulated Markets

Demonstrated Capability to propel Products from Conception to Commercialization

ANDA Products

Product Identification

Product Development

Commercial

Data Analysis – IQVIA, Symphony & Other Data

R&D to establish API Equivalency

Partner Finalization

Concurrent Process

Competitive Landscape

Formulation Development

Product Feasibility

BE Studies

2 - 3 Months

18-2 0 Months

C G T Applicability

Stability Testing

Dossier Compilation

1-2 Months

Filing

Approval

Launch

Immediate Post Compilation

10-15 months post filing

Immediately Post Approval

2nd Highest in terms of proportion of CGT Exclusivity amongst Peers

C G T is granted when FDA determines there is inadequate generic competition Exclusivity Period for 180 days o Competing Generic Versions of the drug cannot be marketed ▪ Allows to establish a foothold in the market ▪ Opportunity for Market Penetration & Revenue

Proportion of Ingredients with CGT Exclusivity

80.0%

75.0%

75.0%

75.0%

60.7%

52.6%

Growth Lower price erosion due to lesser competition

Source: F&S Report Note: All the numbers are as of 30 t h September, 2024

Company 1

Company 3

Company 4

Company 5

Industry Average

19

2

Presence in Regulated Markets through Long -term marketing arrangements

MARKETED PRODUCTS

Business Model

CDMO / CMO

Business Model

Identify, Develop & Commercialize specialty & complex niche products in mid - market range

Customized formulation, development & manufacturing capabilities for customers

Revenue Model

In-Licensing Fee

Transfer Pricing

Profit Sharing

➢ Long-term Marketing & Distribution

Agreements

➢ Strength lies in taking a product from conceptualization to commercialization

➢ 22 Commercialized products

➢ 61 Approved ANDA Products

Revenue Model

Tech Transfer/ Developmental Cost

Transfer Pricing

Service Income

➢ Partner with CDMO customers early in the drug development

process

➢ Recurring Revenue with Steady & Predictable Cash

Flows

➢ Contracts for more than 4 0 products in US, Canada, UK, South Africa, UAE, Israel, Denmark, Saudi Arabia & Vietnam. ➢ Eligible for manufacturing formulations having controlled

substances

➢ Complied for catering to government supplies in the US

Pharmaceutical companies increasingly favor partnering with one-stop-shop solution providers that seamlessly integrate both development and manufacturing services

20

3

Presence in the Emerging Markets with Portfolio Including Specialty and Complex Products

Special Focus

40+ Countries Marketed

921 Total Products

285 Product Registrations

636 Product Applications Filed

87 Commonwealth of Independent States

403 South East Asia

Niche & Specialty patented products in the US with early launch opportunity in Emerging Markets

Sugammadex

Ferric Carboxymaltose

7 3 | 14 Registered | Filed

72|331 Registered | Filed

Tofacitinib

138 Africa

287 LATAM

6 Middle East

Apixaban

Sacubitril + Valsartan

Eltrombopag Olamine

26 | 112 Registered | Filed

113 | 174 Registered | Filed

1 | 5

Registered | Filed

Diverse Business Models

P2P Model

Distributor Model

CDMO Model

Own Brands2

Philippines

Peru

Ghana

Nigeria

Myanmar

Guatemala

Kenya

Top Emerging Markets1

21

Partners to Global Pharmaceutical Companies in Regulated & Emerging Markets

22

Strong R&D Capabilities Driving Differentiated Product Portfolio

Oral Solids

ORS

Injectables

Oral Liquids

API

R&D Site 1 - USA

Identify

▪ In-House R&D in US

for Controlled Substances

R&D Site 2 - India

▪ Helps in dossier

preparation

▪ Submission of ANDA

applications

▪ Internal research ▪ Information available

on subscribed databases

Team

▪ 64 people ▪ 2 members having

doctoral qualifications

R&D Site 3 - India

Margin

Consolidating R&D activities at Ahmedabad. R&D Centre spread around 11,750 sq. ft.

The focus on R&D has allowed the company to maintain high profit margins compared to it’s industry peers

23

5

Accredited Manufacturing Facilities

Atlanta Facility

Facility

2 Manufacturing Lines

185,300 Sq. Ft. Total Area

OSD

1.2 Bn units Annual Installed Capacity

Ahmedabad, Chhatral Facility

Strong Regulatory Track Record

USFDA Approved

4 USFDA, received no Form 483 & 8 Customer Audits

DEA Compliant

Eligible for Manufacturing Controlled Substances

BAA Compliant

Ability to caters to government supplies

General Oral Dosage

1397.96 Mn Annual Installed Capacity1

Injectables

49.92 Mn Annual Installed Capacity1

Facility Approvals

35,205 Sq. Mtr.

Total Area

12 Manufacturing Lines

4 Dosage Forms

Beta Lactum Orals

511.68 Mn Annual Installed Capacity1

24

Corporate Structure

Group holding company based in India Houses Domestic Critical Care Injectables business & API business

Senores Pharmaceuticals Inc. Marketing cum ANDA Holding Company

US based company holding ANDAs and mutually exclusive marketing relationships with customers

Havix Group Inc Caters to Regulated Market

Ratnatris Pharmaceuticals Pvt. Ltd. Caters to Emerging Market

Engaged in the Contract Development & Manufacturing of Generic Pharmaceutical Formulations for the US, Canada

Development, Manufacturing and Marketing of Generic Pharmaceutical Formulations

100% Subsidiary

67.77%1 Subsidiary

69% Subsidiary

Note 1 : 49.91% held by the holding company & 16.66% held by it’s wholly owned subsidiary company named Senores Pharmaceuticals Inc

25

6

Professional and Dedicated Management Team

Swapnil Jatinbhai Shah Promoter & Managing Director

Sanjay Shaileshbhai Majmudar Chairman & Non-Executive, Non- Independent Director

Deval Rajnikant Shah Whole-Time Director & CFO

▪ 17+ years of experience in the pharma sector

▪ 40+ years of experience

▪ Part of the core management team & leads

overall company functions: product portfolio, corporate strategy, business development, strategic management

▪ Director on the board of AIA Engineering Ltd., Ashima Ltd., M&B Engineering Ltd. & Welcast Steels Ltd.

▪ 4 0 + years of experience in Pharma,

Engineering & Chartered Accountancy

▪ Previously associated with SAI Consulting

Engineers Pvt. Ltd. as CFO

Chetan Bipinchandra Shah Whole-Time Director & C O O

Jitendra Babulal Sanghvi Non-Executive, Non-Independent Director

Ashokkumar Vijaysinh Barot Promoter, Non-Executive, Non- Independent Director

Deepak Jain Vice President Regulatory Affairs

▪ 25+ years of experience in Pharma

▪ 15+ years of experience

▪ 21+ years of Pharmaceutical experience

▪ 11+ years of Pharmaceutical experience

▪ Previously associated with Torrent Pharma

▪ Director of Ratnaris Pharma since Aug 11, 2 0 0 9

& Cadila Pharma. Also associated with Reliance Retail Ltd., Reliance Fresh Ltd. & Reliance Corporate IT Park Ltd.

▪ Conferred with “Young Pharma Entrepreneur of

the Year” award in 2013

▪ Non-Executive Director on the board of Di-Cal Pharma Pvt. Ltd. Since Nov 6, 2008. Registered pharmacist with the state pharmacy council of Gujarat

▪ Previously Associated with Cadila Healthcare Ltd.. As Deputy General Manager

26

Growth Strategies

Private & Confidential

Key Strategies

Inorganic growth through synergistic acquisitions

Significantly enhance market presence in North America & other Regulated Markets

Integrated approach by enhancing capabilities for backward integration

Launch products with the potential of NDA approval in the US

Strategic alliance for CMO/CDMO in Regulated Markets

Expanding into new Regulated & Emerging Markets

28

Enhance Market Presence of Marketed Products in North America and Other Regulated Markets

US accounts for 43% of the global pharma market, 56% of the regulated market & 91% of North America Market

Persistent drug shortage calls for an increased supply of generic drugs

Global pharma market by classification (2023, USD bn)

US pharma market size (USD bn)

Number of new drug shortages

7.3%

160

156

114

Regulated

Emerging

23.0%

77.0%

25.3%

12.8%

61.9%1

711.0

1,010.0

Asia

EU

North America

2023

2028F

2021

2022

2023

Enhance market presence in North America along with the partners

Launch generic products with the potential of NDA approval in the US

✓ Set up niche sterile injectables manufacturing facility in the US

✓ Inorganic growth through synergistic acquisitions

Source: F&S Report Note: 1: Pharma market value for North America is USD 778.8 bn, Europe is USD 318.5 bn & Asia is USD 161.3 bn

29

Entering into Strategic Alliance for CMO/CDMO in Regulated Markets

CDMO market growing faster than the pharma market which is growing at 7.7%

US CDMO/CMO market (USD bn)

7.7%

6.8%

32.1

44.7

64.8

2018

2023

2028F

Growth propellers

Growing drug complexity

Rapid technological turnaround

Upcoming loss of exclusivity for drugs

Business model shift from Capex to Opex

Expected Increase in average outsourcing penetration

US accounts for 4 0 - 45% of CD M O markets

Source: F&S Report

Strategic alliance for CMO/CDMO in Regulated Markets

The dependence on CDMO/CMO’s has increased as they offer

Appended Manufacturing Capacity

Mitigate investments, production & supply risk

A c c e ss to new Markets

Bring Technological Overhaul

Eligible for Manufacturing Controlled Substances

Complied to cater to Government Supplies

Offering benefits such as

Focus on core competencies

Co st Advantages

Early to Market advantage

Flexibility & Scalability

A c c e ss to global talent & advanced technologies

30

Expanding into New Regulated & Emerging Markets

Regulated & Emerging markets witnessing strong growth

Global pharma market by classification (USD bn)

Emerging pharma market by Product (2028F)

Regulated pharma market by Product (2028F)

Regulated

Emerging

Innovator

Generic

Generic

Innovator

376.3

1,258.7

2023

541.0

1,710.0

2028F

300.9

240.1

1,423.1

286.8

Expanding into New Regulated & Emerging Markets

Focus on niche and complex range of products with higher margin profile

Leverage presence in Regulated Markets, to increase reach in Semi Regulated Markets

Tapping into new mid-tier markets such as Brazil, Australia & New Zealand

Leveraging knowledge of Emerging markets to manufacture more products by setting up new facilities

Opportunities for registering & marketing value added niche formulations in Emerging Markets: Philippines, Uzbekistan, Peru, Ghana, Tanzania, Kenya, Libya and Guatemala

Multiple marketing and distribution models to enhance presence in Emerging market countries

Source: F&S Report

31

Enhancing Capabilities for Backward Integration

Indian API export market to grow at a CAGR of 8.4%

Pursuing an integrated approach for greater backward integration

API exports (USD bn)

CAGR: 8.4%

7.1

2028F

4.7

2023

Urology

CNS

Alpha Blocker

Anti-Psychotic

Anticonvulsants

Infertility

Cardiovascular

15 APIs across 11 Therapeutic Areas

Antihistamine

Proposed Expansion Plans

Setup Greenfield unit - Increase API manufacturing capacity from 25 MTPA to 169 MTPA

Manufacture API for Regulated and Semi-Regulated markets

Benefits of API manufacturing capabilities

Supply Chain Control

Cost Savings

Quality Assurance

Flexibility & Innovation

Reduced Time to Market

Anti-Inflammatory

Anti-depressant

Oncology

Competitive Advantage

Diversified revenue stream & business resiliance

Backward integration into API manufacturing reduces reliance on third-party vendors & enhances market competitiveness

Source: F&S Report

32

Industry Overview

Private & Confidential

Global Pharma Market

Global pharma market is expected to grow at 6.6% from 2023-28…

…regulated market will continue to dominate the global pharma market

US continues to exert influence on Global pharma market

Global pharma market by product type (USD bn)

Global pharma market by region (USD bn)

Share in global pharma market by region (2028F)

1,635.0

410.3

1,224.7

2,251.0

527.0

1,724.0

1,635.0

376.3

1,258.7

2,251.0

541.0

1,710.0

2023 Innova tor

Generic

2028F

2023 Regulated

2028F

Emergin

g

37.9

471.8

1,010.0

514.5

216.9

US

China

EU

India

RoW

Aging Population

Investments in R&D

Population of people over 6 0 expected to double and reach ~2.1 Bn by 2050, increasing age related conditions

Increasing incidences of chronic diseases

~ 1 in 3 adults have multiple chronic conditions, requiring lifelong use of drugs, with co sts estimated to reach USD 47 tn by 2 0 3 0

Growth Drivers

R&D investments drive market growth by discovering breakthrough treatments for prevalent and emerging diseases by expanding therapeutic segments

Consumer awareness

P o st-C OVID - 19, the O T C segment grew massively due to heightened consumer awareness about health, wellness, and preventive care

Demand from developing nations

Rising instances of chronic conditions and persistent burden of infectious diseases drive dual demand

Source: F&S Report

34

Regulated Pharma Market

Regulated markets to dominate the global pharmaceutical sector, driven by their access to a growing innovative drug market & a thriving generics market

Regulated markets constitute 77% of the global pharmaceutical sector (2023) Global pharma market by classification (USD bn)

North America accounts for 62% of regulated pharma market (2023)

New generics and patent expirations to drive drug market growth

Regulated pharma market by region (USD bn)

Regulated pharma market by product type (USD bn)

1,635.0

376.3

1,258.7

2,251.0

541.0

1,710.0

2023

2028F

Regulated

Emerging

1,258.7

778.8

318.5 161.3

2023

6.8%

Asia

EU

1,710.0

1,085.5

400.3

224.1

2028F North America

1,258.7

234.4

1,024.3

1,710.0

286.8

1,423.1

2023

2028F

Innovator

Generic

US accounts for 43% of the global pharma market, 56% of the regulated market and 91% of North American market (2023)

US Pharma Market size (USD bn)

Characteristics of US healthcare market

7.3%

1,010.0

711.0

High quality standards impose entry barriers

Very high healthcare expenditure per capita

OAI

483s

349

8 0

215

124

466

162

510

142

2020

2021

2022

2023

Healthcare expenditure per capita (USD)

USA

C C A

12,555

6,512

Persistent drug shortage calls for an increased supply of generic drugs

Number of new drug shortages 160

156

114

Increasing generic adoption to navigate high healthcare costs

US Generics market (USD bn)

89

92

96

114

2023

2028F

2021

2022

2023

2021

2022

2023

2028F

Growing drug demand with a simultaneous need to control costs has increased import dependence, particularly from India

Source: F&S Report CCA: Comparable Country Average, OAI: Official Action Indicated

35

Emerging Pharma Market

Emerging pharma market

Overview of India pharma market

Emerging markets to outpace developed ones…

Emerging pharma market size (USD bn)

IPM is amongst the fastest growing in the world…

Indian pharma market size (USD bn)

Oral solids will dominate IPM

Indian pharma market by dosage (2028F, USD bn)

7.5%

9.7%

376.3

2023

541.0

2028F

… driven by population growth, expanding disease burden, & investments in healthcare & infrastructure

Emerging pharma market size by region (USD bn)

36.0

74.7 41.4

168.6

2023

51.2

112.0

56.1

238.1

2028F

Asia

Europe

Latin America Middle East and Africa

Source: F&S Report

23.8

2023

37.9

2028F

…dominated by generic drugs constituting ~96% of drug consumption Indian generic pharma market size (USD bn)

9.8%

22.9

2023

36.6

2028F

6.9

4.7

Oral Solids

Injectibles

Others

26.3

Growth Drivers

Insurance penetration

Increase in chronic patient population

Availability of affordable & innovative generics

Drug access focused government schemes

Growth in hospital business segment

36

SENORES PHARMACEUTICALS LIMITED CONTACT US

Senores Pharmaceuticals Limited

CIN: L24290GJ2017PLC100263

Mr. Deval Shah – Whole Time Director & CFO

investors@senorespharma.com

Strategic Growth Advisors Private Limited

CIN: U74140MH2010PTC204285

Mr. Sagar Shroff / Mr. Tanay Shah sagar.shroff@sgapl.net / tanay.shah@sgapl.net +91 98205 19303 / +91 98333 91899

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