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To,
The Manager Listing
BSE Limited
Corporate Relationship Department
Dalal Street, Mumbai 400 001
Scrip Code: 539268
To,
The Manager Listing
National Stock Exchange of India Limited
Corporate Communication Department
Bandra (EAST), Mumbai 400 051
Scrip Symbol: SYNGENE
Dear Sir/Madam,
Subject: Investor Presentation under regulation 30 of SEBI (Listing Obligations and Disclosure
Requirements) Regulations 2015
This has reference to Regulation 30(6) of the SEBI (Listing Obligations and Disclosure Requirements)
Regulations 2015, please find attached the Investor Presentation for the quarter ended September
30, 2016. The company will use this presentation for any meeting scheduled with analysts or
institutional investors upto December 31, 2016.
The above mentioned Investor Presentation will also be available on website of the Company
www.syngeneintl.com.
Request you to take the same on record.
Yours faithfully,
For Syngene International Limited,
____________
Mayank Verma
Company Secretary
E: Mayank.verma@syngeneintl.com
M: +91 97399 04949
T: + 91 80 2808 2023
Investor Presentation
October 2016
Safe Harbour
Certain statements in this release concerning our future growth prospects are forward-looking statements, which are subject to a
number of risks, uncertainties and assumptions that could cause actual results to differ materially from those contemplated in such
forward-looking statements.
Important factors that could cause actual results to differ materially from our expectations include, amongst others general economic
and business conditions in India, business outlook of our clientele and their research and development efforts our ability to successfully
implement our strategy, our growth and expansion plans and technological changes, changes in the value of the Rupee and other
currencies, changes in the Indian and international interest rates, change in laws and regulations that apply to the Indian and global
biotechnology and pharmaceuticals industries, increasing competition, changes in political conditions in India and changes in the foreign
exchange control regulations in India.
Neither the company, nor its directors and any of the affiliates have any obligation to update or otherwise revise any statements
reflecting circumstances arising after this date or to reflect the occurrence of underlying events, even if the underlying assumptions do
Introduction
Introduction
The Biocon Group
Services Based
Contract Discovery
Syngene ESOP
2.9%
Contract Development
Contract Manufacturing
Product Based
Biosimilars
Promoter
74.5%
Public
22.6%
As of 30th September 2016 , percentages based on actuals, rounded off to nearest 1 place of decimal
Overview
o Established in 1994 as Indias first Contract Research Organization 22+ years of unparalleled experience
o World class Infrastructure audited successfully by US FDA, EMA, AAALAC and major life sciences partners
5
P&L Summary
H1 FY17
H1 FY16
QoQ Change
Revenue
6,097
4,982
22%
EBITDA
2,266
1,628
39%
EBITDA Margin
37%
33%
molecule research.
PAT
1,345
951
PAT Margin
22%
19%
41%
100+
3,300+*
People
- Chemistry
- Preliminary biology
Capabilities
$5 million
$177 million
Investment
11,131
8,716
7,077
95%(1) of
5,542
4,182
2,571(1)
3,639
qualified scientists
2,928
1,404
FY 2012
2,217
1,682
FY 2013
FY 2014
Revenue (INRm)
FY 2015
FY 2016
EBITDA (INRm)
Scalable
Predictable
De-risked
Profitable
Putting Science to Work
Strictly confidential & privileged
Our Industry
Industry Statistics
(US$ bn)
Global R&D Spending
45
152
29
139
2014
2018
2014
2018
11
Source: Frost & Sullivan, IQ4I, Frost & Sullivan, (1) CRO Market refers to global preclinical and development services market and excludes discovery services
67.2
22.7
15.2
43.4
14.7
9.2
24.7
15.8
4.6
15.2
10.5
3.8
22.7
7.5
14.7
4.2
2014
Discovery
Preclinical
12
Source: Frost & Sullivan, IQ4I
2018
2014
Clinical Services
2018
Asia
Source: IQ4I
ROW
Business Overview
Target
Identification
Lead
Generation
Target
Validation
Target
Optimisation
Development
Lead
Selection
Preclinical
Animal
Safety
Commercialisation
Clinical
Ph
I
Ph
II
Ph
III
Drug filing
with FDA &
other global
regulatory
authorities
Product
launch
Manufacture
Marketing/
Phase IV
Syngene offers an Integrated Service Platform for both small and large molecules
14
Small Molecules
Discovery
Development
Manufacturing
Chemistry
Drug Substance
Development
Clinical Supplies
Biology
Specialty Molecules
Commercial Supplies
Large Molecules
Therapeutic Antibody
Discovery & Engineering;
Allied Services
Bioprocess Development
Process Characterisation
Clinical Manufacturing (Microbial & Mammalian)
Wide Spectrum of Services Across a Range of Molecules Including Antibody-Drug Conjugates and Oligonucleotides
15
Target
Identification
Lead
Generation
Target
Validation
Target
Optimisation
Development
Lead
Selection
Preclinical
Animal
Safety
Commercialisation
Clinical
Ph
I
Ph
II
Ph
III
Drug filing
with FDA &
other global
regulatory
authorities
Product
launch
Manufacture
Marketing/
Phase IV
16
Cost Arbitrage
R&D Productivity
Innovation
Dedicated
Play
Multiple Services
Integrated
Play
Capabilities/
Complexity
Single Service
Cluster
Plays
Component
Plays
Small/Short Term
17
Scale/Predictability
Larger/Long Term
Putting Science to Work
Verticals Overview
17
Dedicated centers
Discovery Services
Integrated Services
Dedicated Infrastructure
customized for clients
requirements
Long term, FTE based contracts
Currently 4 in place: BBRC, ANRD,
BGRC and SARC
Development &
Manufacturing Services
Preclinical studies, Stability,
formulation, CMC and Clinical
supplies, Clinical development etc.
Largely FFS based services (both
short and long term)
High renewal rates in
Manufacturing services
19
Candidate
Selection
Lead Optimization
5 Lead
Compounds
20 Lead
Compounds
500 Lead
Compounds
R1
N
Assay development
and in-vitro screening
for ADME/T profiling
N
R2
20
Candidate
Selection
Development
Candidate
Development
Generation of focused
library and further
screening
Development Services
Encompass activities across multiple disciplines as a
molecule moves from pre-clinical to clinical trials
Drug
Substance
Dvpt.
Clinical
Studies
Preclinical
Studies
Drug
product
Dvpt.
optimization)
o Drug product development (pre-formulation and
Bio
analytical
Viral
Testing
Stability
Studies
formulation development)
o Allied services (stability services, viral testing,
bioanalytical)
Manufacturing Services
Small
Molecules
Large
Molecules
22
Capacity Expansion
- Consistent expansion
- FTE services, manufacturing,
formulation, biologics, stability
Customer
Engagement
Forward
Integration
Capacity
Capability
Capability Additions
- New capabilities across multiple
domains incl. the allied sectors
- Stability, analytical & bio-analytical
services, viral testing
- New platforms: siRNA, ADC
Financial Highlights
H1 FY17
H1 FY16
YoY Change
Revenue
6,097
4,982
22%
1,663
1,512
10%
Employee costs
1,506
1,147
31
Gross Margin
2,928
2,323
26%
48%
47%
Other Expenses
662
695
2,266
1,628
EBITDA
25
39%
11,882
9,329
2,344
37%
33%
921
677
36%
1,345
951
41%
22%
19%
(1) Other Assets calculated as (Inventories + Trade Receivables + Unbilled Revenues + Advance Tax + FX premium + Less ( Trade payables + Others current liabilities) at the end of the year
(2) Net cash / (Net debt) calculated as the Cash & cash equivalents (Cash and bank balances + Current investments) less Total debt (Short-term borrowings + Long-term borrowings) at the end of the year
209
11,882
11,133
8,716
7,077
6,097
5,542
4,182
FY2013
FY2014
FY2015
FY2016
H1 FY2017
26
Note: Revenues from FY 2016 is as per Ind AS (Indian Accounting Standards)
35%
17%
18%
19%
20%
22%
34%
34%
30%
31%
1,345
2,266
1,404
FY2012
22%
1,682
2,217
FY2013
FY2014
EBITDA (INRm)
2,928
FY2015
727
3,867
FY2016
H1 FY2017
EBITDA Margin
FY2012
976
1,339
FY2013
FY2014
1,750
FY2015
2,408
FY2016
H1 FY2017
27
Note: EBITDA and PAT from FY 2016 is as per Ind AS (Indian Accounting Standards)
Capital Expenditure
Historical Capital Investments Average Gross Block (INR Mn)
5,610
6,149
6,819
FY2012
FY2013
FY2014
8,255
FY2015
10,169
FY2016
0.73
0.88
1.01
Ratio(1)
1.02
- Formulation centre
1.09
FY2013
FY2014
FY2015
FY2016
- Oligonucleotides
- Viral testing services
- ADCs
Key facility additions during the last three years include dedicated facility for
Abbott, Baxter and first phase of Syngene Research Centre
28
Gross block turnover ratio calculated as the CRAMS revenue of last twelve months divided by average of Gross block at the beginning and end of the year
Managing Risks
Risk
Mitigation
29
THANK YOU
www.syngeneintl.com
Visit www.syngeneintl.com
IR Contact :
Chanderlekha Nayar
+91 80 6775 8821
Chanderlekha.nayar@syngeneintl.com