Suven Life Sciences Limited · NSE:SUVEN

Suven Life Sciences — Investor Presentation (July 2016)

36 slides from Suven Life Sciences's investor presentation, July 2016

  1. Slide 1: A Treasure House of Innovations and Excellence

    A Treasure House of Innovations and Excellence

  2. Slide 2: Company Overview

    Company Overview  Established in 1989  Profitable and dividend paying since listing in 1995 on the NSE and BSE  Established presence across Contract Research and Manufacturing Services (CRAMS) - Leader and Innovator for NCE based Intermediates  Drug Discovery – Focused on CNS segment  World-cla

  3. Slide 3: Suven's Business Model

    SUVEN’S BUSINESS MODEL Drug Discovery Drug Product Delivery Formulation Clinical Chem lib / Lead Lead Clinical Development, Supplies identification / Pre Trial Process Custom comb chem hits Optimization Clinical Research Synthesis Analytical & Manufacturing characterization Supplies Regulatory & Pac

  4. Slide 4: Of Pharmaceutical Relationship

    Of Pharmaceutical Relationship CRAMS •Leader and Innovator for many NCE based intermediates •600+ projects •380+ R&D professionals DDDSS •Generic API’s •Leader in CNS based internal discovery in India •State of the art facility, models •Multiple big Pharma FORMULATIONS relationships •Pharmaceutical

  5. Slide 5: Financials

    Financials Year Ending March '31 2015 2014 Million (Rs) Million (Rs) Income 5,188.73 5,294.36 Pre-R&D EBITDA 2,055.55 2,250.02 Pre-R&D EBITDA Margin 39.62% 42.50% EBITDA 1,426.04 1,680.40 EBITDA Margin 27.48% 31.74% EBIT 1,258.83 1,562.64 EBIT Margin 24.26% 29.52% Financing Costs 54.17 47.09 Taxes 2

  6. Slide 6: Suven Formulation Development Centre

    SUVEN Life Sciences For wlatioi Development Centire

  7. Slide 7: Capabilities Overview

    CAPABILITIES OVERVIEW 110,000+ sq. ft of World-class Infrastructure comprising • Analytical Method Development & Validation Laboratories • Dissolution Testing Laboratory • Wet Chemistry Laboratory • Microbiology Testing Laboratory • Stability Chambers (220,000 L) • Formulation Development Laboratori

  8. Slide 8: FDC Services

    FDC Services Formulation Development Centre -a Natural extension to the existing CRAMS Business Formulation Development NCE’s ANDA’s NDA’s (Differentiated Products) OTC Analytical Development Method development Method Validations Impurity Profiling RS Estimation Microbiology Stability Management Man

  9. Slide 9: Generic/Branded Generic/OTC Product Development

    Generic/Branded Generic/OTC Product Development  Literature Survey  Identification of API Supplier  Patent Review  Quality and Characterization of API  Analytical Development – API  Product Development Strategy Evaluation  Procurement of API / RM / PM / RLD  Lab Scale Development  Analytica

  10. Slide 10: Generic/Branded Generic/OTC Product Manufacturing

    Generic/Branded Generic/OTC Product Manufacturing  Technology Transfer Verification, Modifications & Adoption  Scale up Batch Production /Modifications (Short Term Stability)  Exhibit Batches Production  Exhibit Batches Stability (Short Term & Long Term)  Pivotal BE Supplies  Compilation of Da

  11. Slide 11: Product Development

    Product Development

  12. Slide 12: Solid Dosages

    Solid Dosages  Tablets: Immediate Release, Sustained Release, Delayed Release, Chewable, Orally Disintegrating (ODT) and Multilayered  Capsules: Multi-particulates, Powders, Tablet in Capsule, Enteric Coating and Modified Release  Powders: Immediate Release, Sustained Release, Delayed Release, Po

  13. Slide 13: Oral Liquids

    Oral Liquids  Oral solutions, Syrups and Elixirs,…  Oral suspensions  Immediate Release and Powders for Suspensions  Emulsions

  14. Slide 14: Topicals

    Topicals  Topical Liquids: Rx, OTC and Personal Care Products for Topical Administration  Topical (Semisolids): Rx, OTC and Personal Care Creams, Gels and Ointments for Topical or Oral Administration (dentifrice)  Ear Drops  Sterile Ophthalmic Preparations

  15. Slide 15: Injectables

    Injectables  Terminal Sterilization  Filtration  Lyophilization  Powder Filling

  16. Slide 16: Process Development Capabilities – R&D

    Process Development Capabilities – R&D  High Shear Mixer Granulation (RMG)  Fluid Bed Granulation (Top Spray)  Roller Compaction & Slugging  Tabletting (Conventional, Bilayer & Tablet in Tablet)  Encapsulation (Powder, Pellet & Tablets or combination thereof)  MUPS (Wurster & Extrusion-Spheron

  17. Slide 17: Packaging Development

    Packaging Development  Blister Packing  Strip Packing  Bottle Packing  Bulk Packing  Liquids Packing  Ointments

  18. Slide 18: List of Equipments – R&D

    List of Equipments – R&D S . No. Description Capacity S . No. Description Capacity 1 Vibro Mechanical Sifter 12 inch 13 Core Coated Tablet Press 20 STN 2 Double Cone Blender 2/5/20 lts Homogeniser (Silent 14 0.8 to 2000 ml Crusher) 3 Rapid Mixer Granulator 3/5/10 lts 500gm -1 kg & 3 kg 15 Autocoater

  19. Slide 19: cGMP Pilot / Manufacturing

    cGMP Pilot / Manufacturing

  20. Slide 20: Manufacturing Support

    Manufacturing Support Dosage Forms  Solid  Liquid Support • Scale up Batches • Exhibit Batches • Validation & Commercial Batches • Clinical Supplies • BE/BA Supplies

  21. Slide 21: Solid Dosages

    Solid Dosages  Tablets: Immediate Release, Sustained Release, Delayed Release, Chewable and Orally Dissolving  Capsules: Powders, Multi-particulates and Tablets in Capsules  Powders: Immediate Release, Sustained Release, Delayed Release, Powders for Sachet or Suspension & Taste Masking  Multi pa

  22. Slide 22: Process Capabilities - Solids

    Process Capabilities - Solids  Blending  Controlled Release  Sizing/Milling  Solubility Enhancement  High Shear and Fluid Bed  High and Low Dose Potency Granulation (aqueous or organic  Taste-Masking solvents)  Orally Disintegrating and  Tabletting Chewable Tablets  Encapsulation  Packagi

  23. Slide 23: Process Capabilities - Liquids

    Process Capabilities - Liquids  Topical liquids: Rx, OTC, and Personal care products for topical administration  Oral solutions  Oral suspensions: Immediate Release and Powders for Suspension

  24. Slide 24: Manufacturing Equipment List

    Manufacturing Equipment List S. No Description Capacity S. No Description Capacity Solid Dosage Form Module Semi Automatic self-adhesive 19 1 Multi Mill - labeling machine 2 Vibro Mechanical sifter 600 mm dia Auotmatic Capsule Filling 20 25000 Cap/Hr Machine 3 Rapid Mixer Granulator 75 & 150 L 21 Em

  25. Slide 25: Liquid Oral Facility

    LIQUID ORAL FACILITY Premixing Tank 1000L 2000L Mixing Tank and 2000L Holding Tank

  26. Slide 26: Analytical Services

    Analytical Services/

  27. Slide 27: Analytical Method Development, Validation and Testing

    Analytical Method Development, Validation and Testing  Our fully equipped GLP Analytical Laboratory is well suited for Drug Product Analytical Method Development, Validation and Analysis to support R&D, Exhibit, Clinical, Validation and Commercial activities.  Our Microbiology Lab is equipped to c

  28. Slide 28: Pre-formulation Studies

    Pre-formulation Studies  Excipient Compatibility Studies  Calorimetry by DSC  Forced-Degradation Studies  Solubility Determination  Bulk Powder Characterization

  29. Slide 29: Method Development and Validations, Dissolution, Cleaning Verification

    Method Development and Validations • Assay • Related Substances • Chiral Purity Dissolution • USP Apparatus I • USP Apparatus II Cleaning Verification • Compound Specific Method • Total Organic Carbon (TOC)

  30. Slide 30: Analytical Services: Microbiology Laboratory Instruments

    ANALYTICAL SERVICES MICROBIOLOGY LABORATORY INSTRUMENTS • Horizontal Laminar Air Flow Benches (2 No's) • Incubators (2000 liters) • Cooling Incubator 2-8 °C (400 liters) • Autoclave • Colony Counter • Carl Zeisis Microscope

  31. Slide 31: Analytical Services Infrastructure

    ANALYTICAL SERVICES INFRASTRUCTURE • Walk-in Stability Chambers of 2,20,000 liters Capacity (10 numbers) • Centralized data acquisition for monitoring and trending Temperature and Humidity 24/7. • Stability Studies meeting the ICH Walk-in Stability Chambers Guidelines and any customer specific requi

  32. Slide 32: ICH Stability Storage and Testing

    ICH Stability Storage and Testing  40°C/75% RH  30°C/65% RH  30°C/75% RH Drug Product Delivery  25°C/60% RH  5°C  Photo Stability  Flexible Conditions

  33. Slide 33: Analytical Instrumentation

    Analytical Instrumentation Inductively coupled plasma mass spectroscopy (ICP-MS) HPLCs (DAD, UV & RI) UPLC (DAD & UV) RRLC (DAD) GC-HS LCMS Polari meter FTIR Particle Size Analyzer (Sympatec) Dissolution Tester - Auto Sampler UV-Vis Spectrophotometer Disintegration Tester BIO-DIS Dissolution Apparat

  34. Slide 34: Collaboration - Partnership

    Collaboration - Partnership WE BUILD Customer Focus Speed Transparency Quality Collaboration & Integrity Partnership Value Passion On Time Flexibility

  35. Slide 35: Contact Details

    Contact Details M. Mohan Rao V. Murali Krishna Prasad Vice President – Business General manager – CQO & Site Development Operations Ph: +91 9392483023 Ph: +91 9392483017 Email: mohanrao@suven.com Email: murali@suven.com Regd. Office: Operations Office: Suven Life Sciences Ltd Suven Life Sciences Ltd

  36. Slide 36: Thank You

Suven Life Sciences — Investor Presentation (July 2016) on 6ix