Lowest Price Guaranteed From USD 2,199
Published
February 2016
Pages
321
View Count
9417
Example Insights
Report Description
The biopharmaceutical industry has been witnessing a significant paradigm shift in R&D outsourcing over the last few years. Specialty CROs have emerged as credible players in the market to overcome the shortcomings of full service / traditional CROs. Often, these full service providers offer a wider portfolio of services but fail to align their efforts to meet the requirements of sponsors, primarily the smaller biotech organisations / start-ups. Specialty CROs, on the other hand, specialize in niche areas catering to either specific clinical / preclinical services or providing services in a particular disease area. Oncology, cardiovascular, metabolic disorders and CNS are some of the popular therapeutic areas that have witnessed a rise in the number of specialty CROs. Typically outsourced services include data management, site monitoring and project management but nowadays core services such as pharmacovigilance, target evaluation, formulation development, cell line development, toxicology studies and medical imaging are also being outsourced to these CROs. Specialty CROs are increasingly adopting the strategic CRO model to expand their services and geographical presence in an effort to broaden the scope of serving the global biopharmaceutical industry.
Despite the widening array of services offered by these CROs, they have found it challenging to gain a higher share in the market, which is currently dominated by larger and more well-established players. Considering that a major proportion of revenues for large CROs is generated by big pharma companies, gaps exist when it comes to providing services to smaller pharma / biotech companies. This provides an opportunity to specialty CROs to offer improved, customized and relatively economical services to newer / smaller clients in the sector.
As the demand of novel therapies for various therapeutic areas is expected to rise steadily, we are optimistic about the future of these smaller research firms, which have driven an innovative approach to drug research and development. There are a number of upcoming opportunities that can enrich the service portfolio of speciality CROs gradually strengthening their presence in an otherwise consolidated market.
Scope of the Report
The “Specialty CROs Market, 2016-2025” report delivers a comprehensive study on Contract Research Organizations (CROs) that provide a specialized set of research capabilities centred on a particular stage of clinical development or a range of services in a focused therapeutic area. The outsourcing model has proven to be extremely beneficial to drug developers catering to the unmet research, clinical development and even regulatory needs of both established players and start-ups in the market. The concept of specialty CROs continues to evolve as these organizations adopt new strategies to provide their sponsors improved services in terms of both quality and efficiency. Novel business models and strategic partnerships among established and emerging players have opened new avenues to effectively tackle issues such as rising development costs, inefficient protocols and unorganized business processes.
The report assesses key drivers that have governed the evolution of specialty CROs over the past several years, along with an elaborate discussion on the upcoming trends that will likely shape the market in the coming years. In fact, one of the primary objectives of this study is to develop an understanding of the likely future evolution of the market for specialty CROs over the short-term and long-term.
The study presents an in-depth analysis of a diverse set of specialty CROs on some of the key parameters such as geographical location, types of services being offered and focused therapeutic areas. In addition, it captures the potential growth areas that will likely present opportunities for these companies and sustain the pace of growth. It is worth highlighting that despite the fact that established pharmaceutical companies have in-house R&D and clinical development capabilities, the opportunity for specialty CROs is growing. The future evolution of this market will be primarily driven by the relatively fast paced growth of the overall pharma industry and the innovations / developments taking place in R&D. The report provides short-midterm and long-term market forecasts for the period 2016-2020 and 2020-2025, respectively. To add robustness to our forecast model, we have provided three market scenarios. The conservative, base and optimistic scenarios represent three different tracks of market evolution. The research, analysis and insights presented in this report are backed by a comprehensive survey on capabilities of several specialty CROs. For the purpose of our analysis, we also interviewed important stakeholders in this market to solicit their opinions around the future opportunities and challenges that must be considered for a more inclusive growth.
Contents
Chapter 2 provides an executive summary of the insights captured during our research. The summary offers a high level view on the present scenario of the specialty CRO market and where it is headed in the mid-long term.
Chapter 3 provides a general introduction to CROs. In this chapter, we have discussed, in detail, the evolution of CROs. We have also presented a highly comprehensive CRO services map to highlight the range of services being offered by a large number of CROs operating in different locations worldwide.
Chapter 4 presents specific details on specialty CROs. It provides information about the functioning of specialty CROs along with the specific areas of specialization. We have also discussed the advantages that specialty CROs bring over conventional CROs, focusing on new business models, strategic partnerships and relatively more efficient / integrated business processes.
Chapter 5 provides a holistic global landscape of specialty CROs that we identified in our research. This chapter highlights key aspects of these companies such as their geographical location, year of establishment and R&D capabilities (categorized in terms of specific therapeutic areas and services capabilities offered).
Chapter 6 provides profiles of 18 specialty CROs focused on specialized preclinical / clinical service offering. Each company profile includes an overview of the company, service portfolio, collaborations and associated developments that have recently taken place.
Chapter 7 provides profiles of 12 specialty CROs focused on a particular therapeutic area. Each company profile includes an overview of the company, service portfolio, collaborations and associated developments that have recently taken place.
Chapter 8 is a case study on virtual CROs. We have discussed, in detail, the virtually integrated, cross-functional outsourcing approach implemented by these organizations. In this chapter, we have also focused on various clinical research partnership models that are applied by CROs and their sponsors. The case study also includes profiles of six virtual CROs, some of which are leading players in the market.
Chapter 9 is a case study on full-service CROs. The one-stop-shop approach followed by traditional CROs has been captured in detail in this section. The case study includes profiles of four CROs, some of which are leading players in the market.
Chapter 10 presents a detailed ten year forecast highlighting the future potential for specialty CROs. Due to the uncertainty surrounding some of the key assumptions, we have presented three different evolution scenarios for the overall market.
Chapter 11 highlights important trends that provide opportunities to specialty CRO to consolidate their presence in this competitive market; amongst others, these include Health Economics and Outcomes Research (HEOR) studies, adaptive trials, eClinical solutions and risk-based monitoring (RBM).
Chapter 12 is a collection of transcript of interviews conducted with key players during the course of this study.
Chapter 13 summarises the overall report. In this chapter, we have provided a recap of the key takeaways and our overall opinion on where the market is headed in the mid-long term.
Chapter 14 is an appendix, which provides tabulated data and numbers for all the figures provided in the report.
Chapter 15 is an appendix, which provides a list of companies and organizations mentioned in the report.
Chapter 16 is an appendix, which provides a glossary of the CRO services map.
1. PREFACE
1.1. Scope of the Report
1.2. Research Methodology
1.3. Chapter Outlines
2. EXECUTIVE SUMMARY
3. INTRODUCTION
3.1. History
3.2. Traditional Contract Research Organisations
3.2.1. Services
3.2.2. Current Industry Environment
3.3. Specialty Contract Research Organisations
4. SPECIALTY CROs: AN INTRODUCTION
4.1. Chapter Overview
4.2. Importance of Specialty CROs
5. MARKET OVERVIEW
5.1. Chapter Overview
5.2. Methodology
5.3. Specialty CROs: Global Landscape
5.3.1. Specialty CROs: The Dramatic Rise
5.3.2. Specialty CROs: Distribution by Nature of Specialisation
5.4. Specialty CROs Focused On a Specific Service Capability
5.4.1. Landscape is Well Distributed across Preclinical and Clinical Services
5.4.2. Specialty CROs: Popular Preclinical Services
5.4.3. Specialty CROs: Popular Clinical Services
5.5. Specialty CROs Focused on Specific Therapeutic Area(s)
5.5.1. Oncology is the Most Researched Therapeutic Area
5.5.2. CROs Mostly Located in the US; Europe is a Distant Second
6. SPECIALTY CROs: FOCUSED ON SERVICES
6.1. Chapter Overview
6.2. CROs Focused on Preclinical Service Capabilities
6.2.1. BRI Biopharmaceutical Research
6.2.1.1. Company Overview
6.2.1.2. Focused Clinical Expertise
6.2.1.2.1. API / Clinical Product QC, Dosing Solutions & Materials
6.2.1.2.2. Bioanalytical Assays for Clinical Trials
6.2.1.2.3. Clinical Trial Equipment Rental & PK Sample Collection Kit
6.2.1.2.4. Cynomologus & Rhesus Monkey Hepatocytes & Blood Products
6.2.1.2.5. Drug Candidate Early In Vitro & In Vivo Screening
6.2.1.2.6. In Vitro DMPK & ADME
6.2.1.2.7. In Vivo DMPK & ADME
6.2.1.2.8. Patient Tumor-Derived Xenograft Models at Oncograph™
6.2.1.2.9. Strategic Development of Botanical Drugs
6.2.2. BTS Research
6.2.2.1. Company Overview
6.2.2.2. Focused Clinical Expertise
6.2.2.2.1. Custom Services
6.2.2.2.2. Disease Models
6.2.2.2.3. In Vitro Services
6.2.2.2.4. IND Process
6.2.2.2.5. Medical Devices
6.2.2.2.6. Pharmacology Services
6.2.2.2.7. Toxicology Services
6.2.2.3. Additional Information
6.2.2.3.1. Recent Developments
6.2.2.3.2. Acquisitions
6.2.3. Dorizoe Lifesciences
6.2.3.1. Company Overview
6.2.3.2. Focused Clinical Expertise
6.2.3.2.1. Services and Capabilities
6.2.3.2.2. Customized Services
6.2.4. Fluofarma
6.2.4.1. Company Overview
6.2.4.2. Focused Clinical Expertise
6.2.4.2.1. Assay Development Services
6.2.4.2.1. Cell-based screening services
6.2.4.2.2. In Vitro Drug Profiling Services and Mechanism of Action (MOA) Studies
6.2.4.2.3. Predictive Toxicology Services
6.2.4.2.4. In Vivo Studies
6.2.4.2.5. Biomarker Analysis Services
6.2.4.3. Additional Information
6.2.4.3.1. Collaborations
6.2.4.3.2. Recent Developments
6.2.5. KIYATEC
6.2.5.1. Company Overview
6.2.5.2. Focused Clinical Expertise
6.2.5.2.1. Drug Response Profiling (DRP) Services
6.2.5.3. Additional Information
6.2.5.3.1. Recent Developments
6.2.5.3.2. Funding
6.2.6. Redoxis
6.2.6.1. Company Overview
6.2.6.2. Focused Clinical Expertise
6.2.6.2.1. In Vivo Models
6.2.6.2.2. In Vitro Services
6.2.6.3. Additional Information
6.2.6.3.1. Collaborations
6.2.6.3.2. Recent Developments
6.2.6.3.3. Funding
6.2.7. Spirovation
6.2.7.1. Company Overview
6.2.7.2. Focused Clinical Expertise
6.2.7.2.1. Clinical Assessment
6.2.7.2.2. Functional Screening and Lead Selection
6.2.7.2.3. Target ID and Primary Screening
6.2.7.3. Additional Information
6.2.7.3.1. Facilities
6.2.8. Velesco Pharmaceutical Services
6.2.8.1. Company Overview
6.2.8.2. Focused Clinical Expertise
6.2.8.2.1. Analytical Method Development
6.2.8.2.2. cGMP Manufacturing
6.2.8.2.3. Drug Formulation Development
6.2.8.2.4. Instrumentation
6.2.8.2.5. Pharmaceutical Consulting
6.3. CROs Focused on Clinical Service Capabilities
6.3.1. Almedis
6.3.1.1. Company Overview
6.3.1.2. Focused Clinical Expertise
6.3.1.2.1. Biostatistics
6.3.1.2.2. Clinical Monitoring
6.3.1.2.3. International Clinical Trials
6.3.1.2.4. Local Studies
6.3.1.2.5. Data Management
6.3.1.2.6. Medical Writing
6.3.1.2.7. Training Programs
6.3.2. Applied Healthcare Resource Management
6.3.2.1. Company Overview
6.3.2.2. Focused Clinical Services
6.3.2.3. Additional Information
6.3.2.3.1. Collaborations
6.3.3. CMX Research
6.3.3.1. Company Overview
6.3.3.2. Focused Clinical Expertise
6.3.3.2.1. CRO Services
6.3.3.2.2. Investigator Network
6.3.3.2.3. Investigator-Led Trials (ILTs)
6.3.3.2.4. MDapps™
6.3.4. DSP Clinical Research
6.3.4.1. Company Overview
6.3.4.2. Focused Clinical Expertise
6.3.4.2.1. Data Management
6.3.4.2.2. Monitoring
6.3.4.2.3. Project Management
6.3.4.2.4. Site Management
6.3.4.2.5. Statistics and Medical Writing
6.3.4.2.6. Others
6.3.4.3. Additional Information
6.3.4.3.1. Collaboration
6.3.4.3.2. Recent Developments
6.3.5. DZS Clinical Services
6.3.5.1. Company Overview
6.3.5.2. Focused Clinical Services
6.3.5.2.1. Biostatistics Support and Consulting
6.3.5.2.2. Clinical Data Management
6.3.5.2.3. Clinical Monitoring
6.3.5.2.4. Clinical Project Management
6.3.5.2.5. ClinPlus® eClinical Platform
6.3.5.2.6. Customized FSP Models
6.3.5.2.7. DZS Clinical Sourcing and Staffing
6.3.5.2.8. Medical Coding
6.3.5.2.9. Medical Writing
6.3.5.2.10. Statistical Programming and CDISC Implementation
6.3.5.2.11. SOP Authoring
6.3.6. EthosExcel™
6.3.6.1. Company Overview
6.3.6.2. Focused Clinical Expertise
6.3.6.2.1. Clinical Trial Services
6.3.6.2.2. Clinical Trial Resourcing
6.3.6.2.3. Diversity Consulting
6.3.6.2.4. Investigator and Trial Site Facilitation Services
6.3.6.2.5. Site Management
6.3.7. ICRC-Weyer
6.3.7.1. Company Overview
6.3.7.2. Focused Clinical Expertise
6.3.7.2.1. Biostatistics
6.3.7.2.2. Clinical Data Management
6.3.7.2.3. Medical Review
6.3.7.2.4. Medical Writing
6.3.7.2.5. Safety Writing and Pharmacovigilance
6.3.7.2.6. Scientific Consulting
6.3.7.3. Additional Information
6.3.7.3.1. Expansion of Service Portfolio
6.3.8. Impact Pharmaceutical Services
6.3.8.1. Company Overview
6.3.8.2. Focused Clinical Expertise
6.3.8.2.1. Drug Development Consulting
6.3.8.2.2. Early Phase Clinical Trial Management
6.3.8.2.3. Medical Writing
6.3.8.2.4. Project and Program Management
6.3.8.2.5. Regulatory Affairs
6.3.8.2.6. Regulatory Operations
6.3.9. Research Dynamics Consulting
6.3.9.1. Company Overview
6.3.9.2. Focused Clinical Expertise
6.3.9.2.1. Clinical Monitoring
6.3.9.2.2. Consulting
6.3.9.2.3. GCP Auditing
6.3.9.2.4. Investigator Recruitment
6.3.9.2.5. Project Management
6.3.9.2.6. Site Management
6.3.9.3. Additional Information
6.3.9.3.1. Collaborations
6.3.10. SDS Clinical
6.3.10.1. Company Overview
6.3.10.2. Focused Clinical Expertise
6.3.10.2.1. Clinical Trial Services
6.3.10.2.2. Consulting Services
7. SPECIALTY CROs: FOCUSED ON THERAPEUTIC AREAS
7.1. Chapter Overview
7.2. Specialty CROs Focused on Oncology
7.2.1. Accelovance
7.2.1.1. Company Overview
7.2.1.2. Focused Clinical Expertise
7.2.1.2.1. CRO Services
7.2.1.2.2. Patient Recruitment
7.2.1.2.3. Clinical Call Center
7.2.1.3. Additional Information
7.2.1.3.1. Collaborations
7.2.1.3.2. Site Expansion
7.2.2. Crown Bioscience
7.2.2.1. Company Overview
7.2.2.2. Focused Clinical Expertise
7.2.2.2.1. Biotherapeutics
7.2.2.2.2. Drug Discovery
7.2.2.2.3. Metabolic Diseases
7.2.2.2.4. Oncology
7.2.2.3. Additional Information
7.2.2.3.1. Collaborations
7.2.2.3.2. Service Expansion
7.2.2.3.3. Site Expansion
7.2.2.3.4. Recent Developments
7.2.2.3.5. Funding
7.2.3. MedSource
7.2.3.1. Company Overview
7.2.3.2. Focused Clinical Expertise
7.2.3.2.1. Clinical Data Management and Biostatistics
7.2.3.2.2. Clinical Support
7.2.3.2.3. Clinical Trial Monitoring
7.2.3.2.4. Project Management
7.2.3.2.5. Regulatory Affairs Management
7.2.3.2.6. Study Start-Up
7.2.4. Novella Clinical
7.2.4.1. Company Overview
7.2.4.2. Focused Clinical Expertise
7.2.4.2.1. Clinical Monitoring
7.2.4.2.2. Data Management
7.2.4.2.3. Data Monitoring Committees
7.2.4.2.4. Investigator Strategy & Site Coordination (ISSC)
7.2.4.2.5. Medical Monitoring
7.2.4.2.6. Medical Writing
7.2.4.2.7. Project Management
7.2.4.2.8. Quality Assurance
7.2.4.2.9. Regulatory Affairs
7.2.4.2.10. Safety Management
7.2.4.2.11. Steering Committees & Clinical Advisory Boards
7.2.4.2.12. Training
7.2.4.2.13. Clinical Staffing
7.2.4.2.14. Expertise in Oncology across Various Phases of Clinical Trials
7.3. Specialty CROs Focused on Cardiovascular / Cardiology
7.3.1. Cardialysis
7.3.1.1. Company Overview
7.3.1.2. Focused Clinical Expertise
7.3.1.2.1. Trial Services
7.3.1.2.2. Core Laboratory
7.3.1.2.3. Network of Partners
7.3.1.3. Additional Information
7.3.2. IonsGate Preclinical Services
7.3.2.1. Company Overview
7.3.2.2. Focused Clinical Expertise
7.3.2.2.1. Cell Based Assays
7.3.2.2.2. Isolated Tissue Based Assays
7.3.2.2.3. In Vivo Models
7.4. Specialty CROs Focused on Metabolic Disorders
7.4.1. Betagenex
7.4.1.1. Company Overview
7.4.1.2. Focused Clinical Expertise
7.4.1.2.1. Experimental Services
7.4.1.2.2. Consulting Services
7.4.1.3. Additional Information
7.4.2. Physiogenex
7.4.2.1. Company Overview
7.4.2.2. Focused Clinical Expertise
7.4.2.2.1. Research Services
7.4.2.2.2. Consultancy Services
7.4.2.3. Additional Information
7.4.2.3.1. Collaborations
7.4.2.3.2. Recent Developments
7.4.3. Profil Institute
7.4.3.1. Company Overview
7.4.3.2. Focused Clinical Expertise
7.4.3.2.1. Clinical Development
7.4.3.2.2. Clinical Research
7.4.3.2.3. Data Management and Statistical Services
7.4.3.2.4. Monitoring, Quality & Compliance
7.4.3.2.5. Recruitment Services
7.4.3.2.6. Regulatory Affairs
7.4.3.2.7. Scientific Services
7.4.3.2.8. Experience in Metabolic Disorders
7.4.3.3. Additional Information
7.4.3.3.1. Collaborations
7.5. Specialty CROs Focused on CNS
7.5.1. Biospective
7.5.1.1. Company Overview
7.5.1.2. Focused Clinical Expertise
7.5.1.2.1. Image Processing Technology
7.5.1.2.2. Rodent Models
7.5.1.2.3. Animal Imaging
7.5.1.2.4. Human Imaging and Clinical Trials
7.5.1.2.5. Histology and IHC
7.5.2. RenaSci
7.5.2.1. Company Overview
7.5.2.2. Focused Clinical Expertise
7.5.2.2.1. Experimental Services
7.5.2.2.2. Consultancy Services
7.5.2.3. Additional Information
7.5.2.3.1. Recent Developments
7.5.3. RxGen
7.5.3.1. Company Overview
7.5.3.2. Focused Clinical Expertise
7.5.3.2.1. Efficacy Models
7.5.3.2.2. Custom Model Development
7.5.3.2.3. Pharmacokinetics, Pharmacodynamics and Delivery Optimization Services
7.5.3.2.4. Toxicology and Safety Pharmacology
7.5.3.2.5. Supporting Technologies & Capabilities
7.5.3.3. Additional Information
7.5.3.3.1. Collaboration
7.5.3.3.2. Funding
7.5.3.3.3. Recent Developments
8. CASE STUDY I: VIRTUAL CROs
8.1. Introduction to Virtual CROs
8.2. Frestedt
8.2.1. Company Overview
8.2.2. Service Portfolio
8.2.2.1. Clinical Research
8.2.2.2. Regulatory Affairs
8.2.2.3. Quality Systems
8.3. InSymbiosis
8.3.1. Company Overview
8.3.2. Service Portfolio
8.3.2.1. Drug Discovery
8.3.2.2. Lead Optimization and Efficacy Model
8.3.2.3. Non-Clinical Safety Studies and Bioanalysis
8.3.2.4. Regulatory IND / IMPD filings
8.3.2.5. Document Management
8.3.2.6. Phase I / II/ III Clinical Studies
8.3.2.7. Collaborations
8.3.3. Additional Information
8.3.3.1. Recent Developments
8.4. Osiris Pharma
8.4.1. Company Overview
8.4.2. Service Portfolio
8.4.2.1. Program Management
8.4.2.2. Consultancy
8.4.2.3. Non-clinical Assessment and Management
8.4.2.4. Preclinical Toxicology and Safety Studies
8.4.2.5. Communication and Monitoring
8.4.2.6. Writing and Reviewing of Reports
8.4.2.7. Other Services
8.5. ProjectPharm
8.5.1. Company Overview
8.5.2. Service Portfolio
8.5.2.1. Virtual CRO
8.5.2.2. Project Management Consulting / Organizational Project Management
8.5.2.3. Vendor Selection
8.5.2.4. Financial Audits
8.5.2.5. Training
8.5.2.6. Rescue Studies
8.5.2.7. Study Start-Up
8.6. The Harte Group
8.6.1. Company Overview
8.6.2. Service Portfolio
8.6.2.1. Virtual CRO
8.6.2.2. Consultation
8.6.2.3. Clinical Trial Project Management
8.6.2.4. Integrated Project Delivery and Accountability
8.7. VxP Pharma
8.7.1. Company Overview
8.7.2. Service Portfolio
8.7.2.1. Chemical Development
8.7.2.2. Preclinical
8.7.2.3. Preformulation and Solid State Chemistry
8.7.2.4. Analytical and Bioanalytical
8.7.2.4.1. Analytical Method Development and Validation
8.7.2.4.2. Extractables and Leachables Studies
8.7.2.4.3. Particle Size Determination
8.7.2.4.4. Container-API Compatibility
8.7.2.4.5. Material Characterization
8.7.2.4.6. Forced Degradation and Stability Studies
8.7.2.4.7. Drug Device Compatibility Studies
8.7.2.4.8. Microbial Testing
8.7.2.4.9. Bioanalytical Testing
8.7.2.5. Formulation Development and Clinical Trial materials
8.7.2.6. Parenteral and Lyophilized Clinical Trial Materials
8.7.2.7. Clinical Packaging and Distribution
8.7.2.8. Commercial Services
9. CASE STUDY II: FULL SERVICE CROs
9.1. Introduction to Traditional CROs
9.2. Covance
9.2.1. Company Overview
9.2.2. Service Portfolio
9.2.2.1. Analytical Services
9.2.2.2. Clinical Development
9.2.2.3. Clinical Testing
9.2.2.4. Consulting
9.2.2.5. Health Economics & Market Access
9.2.2.6. Lead Optimization
9.2.2.7. Manufacturing Services
9.2.2.8. Research
9.2.2.9. Safety Assessment
9.2.3. Collaborations
9.3. Medis Research Group
9.3.1. Company Overview
9.3.2 Focused Clinical Expertise
9.3.2.1. Biostatistics
9.3.2.2. Data Management
9.3.2.3. Medical Writing
9.3.2.4. Oncology Expertise
9.3.2.5. Pharmacovigilance
9.3.2.6. Proofreading and Translation
9.3.2.7. RDC System ODM QuaSi®
9.3.2.8. Regulatory Services
9.3.2.9. Scientific Consulting
9.3.2.10. Study Documentation
9.3.2.11. Study Management
9.3.2.12. Study Monitoring
9.3.2.3. Clinical Trial Phase Expertise
9.3.2.4. Additional Information
9.4. Quintiles
9.4.1. Company Overview
9.4.2. Service Portfolio
9.4.2.1. Clinical Trial Execution
9.4.2.2. Consulting
9.4.2.3. Laboratories
9.4.2.4. Real-World and Late Phase
9.4.2.5. Patient and Provider Engagement
9.4.2.6. Product Marketing and Sales
9.4.2.7. Technology Solutions
9.4.2.8. Portfolio and Strategic Planning
9.4.3. Financial Performance
9.4.4. Collaborations
9.4.5. Recent Developments
9.5. Triclinium Clinical Trial Project Management
9.5.1. Company Overview
9.5.1.1. Focused Clinical Expertise
9.5.1.2. Additional Information
9.5.1.2.1. Collaborations
10. MARKET FORECAST
10.1. Chapter Overview
10.2. Forecast Methodology
10.3. Global Specialty CROs Market, 2015-2025
10.4. Regional Specialty CROs Market, 2015 – 2025
11. FUTURE OPPORTUNITIES
11.1. Chapter Overview
11.2 The Changing Scenario of Outsourcing
11.3. Health Economics and Outcomes Research (HEOR) Studies
11.4. Adaptive Trial Design
11.5. eClinical Solutions
11.6. Risk Based Monitoring (RBM)
11.7. Digital CRO (dCRO)
12. CONCLUSION
12.1. A Widening Portfolio of Services Governed by Industry Constraints
12.2. Closer Working Collaboration is the Key to Success
12.3. Within Therapeutic Areas, Oncology is the Flagbearer
12.4. Due to Several Niche Offerings, Specialty CRO Market Remains Fragmented
12.5. The Market of Specialty CROs is Likely to Sustain the Growth Momentum
12.6. Untapped Opportunity Areas will Emerge as Key Growth Drivers in the Long-Term
12.7. Concluding Remarks
13. INTERVIEW TRANSCRIPTS
13.1. Chapter Overview
13.2. Raf Magar, President, CRO and Outcomes Research, AHRM
13.3. Jeffrey P. Kiplinger, President, Averica Discovery Services
14. APPENDIX 1: TABULATED DATA
15. APPENDIX 2: LIST OF COMPANIES AND ORGANISATIONS
16. APPENDIX 3: SERVICE MAP GLOSSARY
Figure 4.1 Specialty CROs: Benefits
Figure 4.2 Specialty CROs: Areas of Specialization
Figure 5.1 Specialty CROs: Distribution on the Basis of Year of Foundation
Figure 5.2 Specialty CROs: Distribution by Nature of Specialization
Figure 5.3 Specialty CRO Services: Stage of Development
Figure 5.4 Specialty CROs: Focused Preclinical Services
Figure 5.5 Specialty CROs: Focused Clinical Services
Figure 5.6 Specialty CROs: Distribution by Focused Therapeutic Areas
Figure 5.7 Specialty CROs: Geographical Distribution by Therapeutic Area
Figure 6.1 Specialty CROs: Focused Capabilities
Figure 6.2 BTS Research: Services for Custom Monoclonal and Polyclonal Antibody
Figure 6.3 Dorizoe Lifesciences: Dosage Forms
Figure 6.4 Dorizoe Lifesciences: Formulation Development Protocol
Figure 6.5 Dorizoe Lifesciences: Customized Services
Figure 6.6 Spirovation: Samples and Biomarkers used for Biomarker Evaluation
Figure 6.7 Velesco Pharmaceutical Services: Portfolio
Figure 6.8 ICRC-Weyer: Biostatistical Services
Figure 6.9 ICRC-Weyer: Safety Writing and Pharmacovigilance
Figure 6.10 Impact Pharmaceuticals: Medical Writing
Figure 7.1 Specialty CROs: Focused Therapeutic Area(S)
Figure 7.2 Novella Clinical: EDC and Supporting Systems
Figure 7.3 Novella Clinical: Project Management Cycle
Figure 7.4 Novella Clinical: Oncological Trial Experience (%)
Figure 7.5 Physiogenex: Preclinical Services for First Level Phenotyping and Screening
Figure 7.6 Profil Institute: Expertise in Anti-Diabetes Compounds
Figure 7.7 Profil Institute: Expertise in Anti-Obesity Compounds and Devices
Figure 7.8 Biospective: Rodent Models
Figure 7.9 Biospective: Imaging Services For 1.5 and 3T MRI and Brain Pet Studies
Figure 7.10 Biospective: Therapeutic Areas for Human Imaging
Figure 7.11 Biospective: Services for Quantitative Image Analysis
Figure 7.12 Biospective: Stains for Histology and Immunochemistry Studies
Figure 8.1 Frestedt: Service Portfolio
Figure 8.2 ProjectPharm: Consulting Services
Figure 8.3 The Harte Group: Clinical Trial Project Management Services
Figure 8.4 VxP Pharma: GLP Radiolabelling Studies
Figure 8.5 VxP Pharma: Mammalian and Viral Cell Banks
Figure 9.1 Quintiles: Service Revenue, 2010-H1 2015 (USD Million)
Figure 10.1 Overall Specialty CROs Market, Short-Midterm (2015-2020): Base Scenario (USD Billion)
Figure 10.2 Overall Specialty CROs Market, Long Term (2020-2025): Base Scenario (USD Billion)
Figure 10.3 Regional Market Forecast, 2015, 2020 And 2025: Base Scenario (USD Billion)
Figure 11.1 Specialty CROs: Future Opportunities
Table 5.1 Specialty CROs: Global Landscape
Table 5.2 List of Specialty CROs and their Service Capabilities
Table 5.3 Specialty CROs: Classification by Therapeutic Areas
Table 6.1 BTS Research: Animal Models for Immune and Inflammatory Diseases
Table 6.2 BTS Research: Animal Models for Oncology
Table 6.3 BTS Research: Animal Models for CNS
Table 7.1 Accelovance China: Services
Table 7.2 MedSource: Research Experience in Oncology by Type of Indication
Table 7.3 Physiogenex: Animal Models for Diabetes
Table 7.4 Physiogenex: Technology Platform for Diabetes
Table 7.5 Physiogenex: Animal Models for Dyslipidemia
Table 7.6 Physiogenex: Technology Platform for Dyslipidemia
Table 7.7 Physiogenex: Animal Models for NAFLD/NASH
Table 7.8 Physiogenex: Technology Platform for NAFLD/NASH
Table 7.9 Physiogenex: Animal Models for Obesity
Table 7.10 Physiogenex: Technology Platform for Obesity
Table 7.11 Physiogenex: Animal Models for Nutraceuticals
Table 7.12 Physiogenex: Technology Platforms for Nutraceuticals
Table 8.1 VxP Pharma: Systems Suitable for E/L testing
Table 14.1 Specialty CROs: Distribution by Year of Foundation
Table 14.2 Specialty CROs: Distribution by Nature of Specialization
Table 14.3 Specialty CRO Services: Stage of Development
Table 14.4 Specialty CROs: Focused Preclinical Services
Table 14.5 Specialty CROs: Focused Clinical Services
Table 14.6 Specialty CROs: Distribution by Focused Therapeutic Areas
Table 14.7 Specialty CROs: Geographical Distribution by Therapeutic Area
Table 14.8 Novella Clinical: Oncological Trial Experience (%)
Table 14.9 Quintiles: Service Revenue, 2010-H1 2015 (USD Million)
Table 14.10 Overall Specialty CROs Market, Short-Midterm (2015-2020): Base Scenario (USD Billion)
Table 14.11 Overall Specialty CROs Market, Long Term (2020-2025): Base Scenario (USD Billion)
Table 14.12 Regional Market Forecast, 2015, 2020 and 2025: Base Scenario (USD Billion)
Table 14.13 Overall Specialty CROs Market, Short-Midterm (2015-2020): Conservative Scenario (USD Billion)
Table 14.14 Overall Specialty CROs Market, Long Term (2020-2025): Conservative Scenario (USD Billion)
Table 14.15 Regional Market Forecast, 2015, 2020 and 2025: Conservative Scenario (USD Billion)
Table 14.16 Overall Specialty CROs Market, Short-Midterm (2015-2020): Optimistic Scenario (USD Billion)
Table 14.17 Overall Specialty CROs Market, Long Term (2020-2025): Optimistic Scenario (USD Billion)
Table 14.18 Regional Market Forecast, 2015, 2020 and 2025: Optimistic Scenario (USD Billion)
Table 14.19 Specialty CROs Market: Comparative Market Evolution Scenarios, 2015, 2020 and 2025 (USD Billion)
The following companies and organisations have been mentioned in this report.