Product Code: Sample_Regulatory Affairs Outsourcing Market - Global Outlook & Forecast 2022-2027_Arizton.pdf
The Global Regulatory Affairs Outsourcing Market is expected to grow at a CAGR of 12.73%.
The following factors will drive the global regulatory affairs outsourcing market growth during the forecast period:
- Increasing Use of Digital Platforms/Solutions in Regulatory Affairs
- Changing Regulatory Landscape
- Rising Demand For Fast Drug & Medical Device Approvals
- Impact of Strict Government Regulations
REGULATORY AFFAIRS OUTSOURCING MARKET SCENARIO
RA serves as the interface between the regulatory authorities and companies, acts as the channel of communication with the regulatory authorities as to the approval process proceeds, and ensures that the approval will be executed effectively. RA outsourcing companies help biopharma and MedTech companies handle regulatory approval workflows flexibly, productively, and efficiently. Regulatory affairs service providers offer comprehensive services to companies, from strategic regulatory advice to regulatory maintenance and lifecycle support. It is the responsibility of RA outsourcing companies to keep abreast of current legislation, guidelines, and other regulatory intelligence.
- Across the world, there have been growing cases of chronic illness or infectious diseases, patent expirations of prescription biologics, developments of biosimilars/orphan drugs and cell and gene therapy products, brand extensions, easy accessibility of OTC drugs across various platforms, economic and social factors, increasing healthcare expenditures, and advancements in regulatory affairs outsourcing, which are increasing the demand for regulatory affairs outsourcing services.
- The healthcare industry is witnessing new compounds originating outside the companies ultimately responsible for marketing them. For instance, around one-third of approved drugs commercialized by big pharma/biotech companies were sourced from outside a decade ago. Approximately 50% to 70% of large companies' pipeline molecules are currently sourced outside.
- In recent years, both pharma and medical device industries have witnessed many M&As, with oncology, orthopedic, and cardiovascular diseases being a particular area of interest. For instance, the pharma industry saw around 2,880 deals worth more than $1 trillion between 2014 and the first half of 2019 in gene therapy, immuno-oncology, microbiome, and orphan drugs.
- The healthcare regulatory affairs outsourcing market is highly competitive and competes with traditional CROs and in-house regulatory affairs departments in pharma/biotech and medical device companies.
Increasing Development of Biosimilars, Orphan Drugs, and Personalized Medicines
- Over the last two decades, a transformation has occurred in treating many chronic and highly complex diseases like autoimmune disorders, cancer, and diabetes, introducing biopharmaceuticals.
- Over the next five years, it is expected that the number of biosimilars and their market authorization will increase significantly as top-selling biologics such as Herceptin (Trastuzumab; Roche/Genentech), Enbrel (Etanercept; Amgen), Humalog (Insulin Lispro;), MabThera (Ritziximab; Roche, Basel), and Aranep (Darbepoetin Alpha; Amgen) go off patent.
- Pfizer has agreed with Biocon (India) to produce biosimilar insulin. Eli Lilly and AstraZeneca have announced plans to produce biosimilars, and Boehringer Ingelheim has established a specialized business to develop and sell biosimilars.
- Another challenge for pharmaceutical companies and other life sciences companies is anticipating the regulation of personalized medicine such as gene therapy and cell therapy. As R&D related to human cell and gene therapy grows rapidly, all stakeholders need to be aware of regulatory changes quickly.
The emergence of Virtual Trials and Virtual Communication
- Many regulatory authorities around the globe issued guidance documents containing information on how trials could continue during the pandemic, which includes the US Food and Drug Administration (FDA), European Medicines Agency (EMA), Medicines and Healthcare Products Regulatory Agency (MHRA), and Singapore's Health Science Authority.
- The COVID-19 pandemic has energized the ascent of clinical trials without clinical sites and made way for proceeding with these inventive models after the general well-being emergency has blurred.
- A constellation of emerging technology and services has permitted the relocation of clinical-trial activities closer to patients. Without in-person visits, investigators can maintain relationships with study participants using electronic consent, telehealthcare, remote patient monitoring, and electronic clinical outcome assessments (eCOAs).
- Before the pandemic, an Industry Standard Research survey in December 2019 found that 38% of pharma and contract research organizations (CROs) expected virtual trials to be a major part of their portfolios, and 48% expected to run a trial with most activities taking place in participants' homes.
- Sponsors and service providers attempting to execute decentralized trials must manage technological and approach uncertainties while balancing the demands of each stakeholder group and providing a good, distinctive experience.
Changing Regulatory Landscape
- In recent years, life sciences companies have faced increasing pressure, including regulatory requirements, technological advances, and pricing pressure. COVID-19 has only provided more reasons for modernizing compliance and improving values and partnerships within the organization and with external stakeholders.
- A recent global survey of pharmaceutical company CEOs reveals that regulations are being scrutinized for many aspects of business, including sales and marketing practices, government reporting of drug prices, privacy controls, and clinical practice.
- Changes in the regulation viewed it as one of the top three disruptive business trends facing pharmaceutical and life sciences companies. Large pharmaceutical companies recognize these changes as the greatest threat to their potential future growth.
- Contract research organizations (CROs) are well experienced and have updated on all changes in regulatory affairs in the pharmaceutical or the medical device industry. Thus, the pharmaceutical and medical devices companies are increasingly outsourcing the regulatory affairs activities to CROs.
GLOBAL REGULATORY AFFAIRS OUTSOURCING MARKET SEGMENTS
The small molecules drugs market size will cross USD 3 billion in 2022. For many decades, small molecule drug compounds have been the mainstay of the pharmaceutical industry. Small molecule drugs continue to play an essential role in developing new therapies globally. The demand for small molecule drugs remains high, with around 97% of the commercial drugs available in the market classified as small molecules.
The biologics segment will likely witness a faster growth rate due to a surge in demand for biopharmaceuticals like mAbs, vaccines, cell & gene therapies, recombinant proteins, etc.
Major Biologics & Their Revenue in 2019 & 2020
- In 2020, one of the key companies, AbbVie, has sold around USD 19.8 billion worth of HUMIRA drugs compared to USD 19.1 billion in 2019, which shows an increment of almost 3.5% in sales.
- Johnson & Johnson sold approximately USD 7.7 billion worth of STELARA drugs in 2020, compared to USD 6.3 billion in 2019, representing a more than 21% increase in sales.
- In 2020, Merck & Co. sold around USD 14 billion worth of KEYTRUDA drugs, up from USD 11 billion in 2019. This is a more than 29% increase in sales.
The small & mid-sized companies reported a major share of around 63.73% of the global regulatory affairs outsourcing market. Small and Medium-sized companies are leading because small and Medium-sized pharmaceutical companies outsource about 90% and 75% of their regulatory requirements. These companies often face resource and technology shortages and partner with suppliers on a project basis.
The pharma & biotech companies market reported a major share of around 65.19%. Pharmaceutical and biotechnology companies have partnered with contract research organizations (CROs) for outsourcing needs, including regulatory services. Most companies choose CROs for outsourcing regulatory services. They believe that regulatory outsourcing companies have the conceptual and technical expertise to achieve efficient results.
The pre-authorization market reported a major share of around 55.48% of the global regulatory affairs outsourcing market. US and EU health authorities require most regulatory applications to be received in ICH harmonized CTD format in the current regulatory era. A thorough submission approach and standardized CTD document templates enable effective regulatory submissions and subsequent lifecycle management with shorter and cost-effective parameters.
The North American region dominates the regulatory affairs outsourcing market with around 33% of the market share. The US is the major revenue contributor to the North American regulatory affairs outsourcing market and accounted for around 91% in 2021. The region's growth is primarily attributed to the increasing number of chronic diseases, development of biologics & biosimilars, increasing healthcare expenditures, and increasing innovation & advancements in regulatory affairs outsourcing.
Segmentation by Product
- Small Molecule Drugs
- Biologics
- Medical Devices
- Others
Segmentation by Company Size
- Small & Mid-Sized Companies
- Large-sized Companies
Segmentation by End-User
- Pharma & Biotech Companies
- Medical Device Companies
- Other Companies
Segmentation by Service Type
- Pre-Authorization
- Marketing Authorization
- Post-Authorization
Segmentation by Region
- North America
- Europe
- Germany
- France
- UK
- Italy
- Spain
- APAC
- China
- Japan
- Australia
- South Korea
- India
- Latin America
- Middle East & Africa
- Turkey
- Saudi Arabia
- UAE
- South Africa
Key Vendors
- Genpact
- Labcorp Drug Development
- Freyr
- ICON
- IQVIA
- Medpace
- Parexel International
- PPD
Other Prominent Vendors
- Accenture
- BlueReg
- Intertek Group
- Lachman Consultants
- NDA Group
- ProPharma Group
- PharmaLex
- Pharmexon
- Promedica International
- CRITERIUM
- Dicentra
- Nuventra Pharma Sciences
- PharmaLeaf
- MAVEN REGULATORY SOLUTIONS
- Global Regulatory Partners
- Sofpromed
- Charles River Laboratories
- Cambridge Regulatory Services
- APC Group
- Real Regulatory
- Voisin Consulting Life Sciences (VCLS)
- Regulatory Pharma Net
- Biomapas
- REGENOLD
KEY QUESTIONS ANSWERED
- 1. What will be the size of the Regulatory Affairs Outsourcing Market by 2028?
- 2. What are the factors driving the market growth?
- 3. Who are the key vendors in the regulatory affairs outsourcing industry?
- 4. Which region holds the highest growth rate in the regulatory affairs outsourcing industry?
TABLE OF CONTENTS
1 RESEARCH METHODOLOGY
2 RESEARCH OBJECTIVES
3 RESEARCH PROCESS
4 SCOPE & COVERAGE
- 4.1 MARKET DEFINITION
- 4.1.1 INCLUSIONS
- 4.1.2 EXCLUSIONS
- 4.1.3 MARKET ESTIMATION CAVEATS
- 4.2 BASE YEAR
- 4.3 SCOPE OF THE STUDY
- 4.4 MARKET SEGMENTATION
- 4.4.1 MARKET SEGMENTATION BY PRODUCT
- 4.4.2 MARKET SEGMENTATION BY COMPANY SIZE
- 4.4.3 MARKET SEGMENTATION BY END-USER
- 4.4.4 MARKET SEGMENTATION BY SERVICE TYPE
- 4.4.5 MARKET SEGMENTATION BY GEOGRAPHY
5 REPORT ASSUMPTIONS & CAVEATS
- 5.1 KEY CAVEATS
- 5.2 CURRENCY CONVERSION
- 5.3 MARKET DERIVATION
6 MARKET AT A GLANCE
7 INTRODUCTION
- 7.1 OVERVIEW
- 7.1.1 THE NEED FOR REGULATORY AFFAIRS
- 7.1.2 ROLE OF REGULATORY BODIES/AGENCIES
- 7.1.3 REASONS TO OUTSOURCE REGULATORY AFFAIRS
8 MARKET OPPORTUNITIES & TRENDS
- 8.1 INCREASING DEVELOPMENT OF BIOSIMILARS, ORPHAN DRUGS, AND PERSONALIZED MEDICINES
- 8.2 IMPACT OF COVID-19
- 8.3 ADVANCEMENTS IN REGULATORY AFFAIRS SERVICES
- 8.4 EMERGENCE OF VIRTUAL TRIALS & VIRTUAL COMMUNICATION
9 MARKET GROWTH ENABLERS
- 9.1 INCREASING USE OF DIGITAL PLATFORMS/SOLUTIONS IN REGULATORY AFFAIRS
- 9.2 CHANGING REGULATORY LANDSCAPE
- 9.3 RISING DEMAND FOR FAST DRUG & MEDICAL DEVICE APPROVALS
- 9.4 STRICT GOVERNMENT REGULATIONS
10 MARKET RESTRAINTS
- 10.1 CONCERNS OVER DATA BREACHES & PRIVACY ISSUES AMONG END-USERS
- 10.2 DEARTH OF SKILLED PROFESSIONALS IN REGULATORY AFFAIRS OUTSOURCING
- 10.3 LACK OF STANDARDIZATION & MONITORING ISSUES IN REGULATORY AFFAIRS
11 MARKET LANDSCAPE
- 11.1 MARKET OVERVIEW
- 11.2 MARKET SIZE & FORECAST
- 11.2.1 INSIGHTS BY GEOGRAPHY
- 11.2.2 INSIGHTS BY PRODUCT
- 11.2.3 INSIGHTS BY COMPANY SIZE
- 11.2.4 INSIGHTS BY END-USER
- 11.2.5 INSIGHTS BY SERVICE TYPE
- 11.3 FIVE FORCES ANALYSIS
- 11.3.1 THREAT OF NEW ENTRANTS
- 11.3.2 BARGAINING POWER OF SUPPLIERS
- 11.3.3 BARGAINING POWER OF BUYERS
- 11.3.4 THREAT OF SUBSTITUTES
- 11.3.5 COMPETITIVE RIVALRY
12 PRODUCT
- 12.1 MARKET SNAPSHOT & GROWTH ENGINE
- 12.2 MARKET OVERVIEW
- 12.3 SMALL MOLECULE DRUGS
- 12.3.1 MARKET OVERVIEW
- 12.3.2 MARKET SIZE & FORECAST
- 12.3.3 SMALL MOLECULE DRUGS: GEOGRAPHY SEGMENTATION
- 12.4 BIOLOGICS
- 12.4.1 MARKET OVERVIEW
- 12.4.2 MARKET SIZE & FORECAST
- 12.4.3 BIOLOGICS: GEOGRAPHY SEGMENTATION
- 12.5 MEDICAL DEVICES
- 12.5.1 MARKET OVERVIEW
- 12.5.2 MARKET SIZE & FORECAST
- 12.5.3 MEDICAL DEVICES: GEOGRAPHY SEGMENTATION
- 12.6 OTHERS
- 12.6.1 MARKET OVERVIEW
- 12.6.2 MARKET SIZE & FORECAST
- 12.6.3 OTHERS: GEOGRAPHY SEGMENTATION
13 COMPANY SIZE
- 13.1 MARKET SNAPSHOT & GROWTH ENGINE
- 13.2 MARKET OVERVIEW
- 13.3 SMALL & MID-SIZED COMPANIES
- 13.3.1 MARKET OVERVIEW
- 13.3.2 MARKET SIZE & FORECAST
- 13.3.3 SMALL & MID-SIZED COMPANIES: GEOGRAPHY SEGMENTATION
- 13.4 LARGE-SIZED COMPANIES
- 13.4.1 MARKET OVERVIEW
- 13.4.2 MARKET SIZE & FORECAST
- 13.4.3 LARGE-SIZED COMPANIES: GEOGRAPHY SEGMENTATION
14 END-USER
- 14.1 MARKET SNAPSHOT & GROWTH ENGINE
- 14.2 MARKET OVERVIEW
- 14.3 PHARMA & BIOTECH COMPANIES
- 14.3.1 MARKET OVERVIEW
- 14.3.2 MARKET SIZE & FORECAST
- 14.3.3 PHARMA & BIOTECH COMPANIES: GEOGRAPHY SEGMENTATION
- 14.4 MEDICAL DEVICE COMPANIES
- 14.4.1 MARKET OVERVIEW
- 14.4.2 MARKET SIZE & FORECAST
- 14.4.3 MEDICAL DEVICE COMPANIES: GEOGRAPHY SEGMENTATION
- 14.5 OTHER COMPANIES
- 14.5.1 MARKET OVERVIEW
- 14.5.2 MARKET SIZE & FORECAST
- 14.5.3 OTHER COMPANIES: GEOGRAPHY SEGMENTATION
15 SERVICE TYPE
- 15.1 MARKET SNAPSHOT & GROWTH ENGINE
- 15.2 MARKET OVERVIEW
- 15.3 PRE-AUTHORIZATION
- 15.3.1 MARKET OVERVIEW
- 15.3.2 MARKET SIZE & FORECAST
- 15.3.3 PRE-AUTHORIZATION: GEOGRAPHY SEGMENTATION
- 15.4 MARKETING AUTHORIZATION
- 15.4.1 MARKET OVERVIEW
- 15.4.2 MARKET SIZE & FORECAST
- 15.4.3 MARKETING AUTHORIZATION: GEOGRAPHY SEGMENTATION
- 15.5 POST-AUTHORIZATION
- 15.5.1 MARKET OVERVIEW
- 15.5.2 MARKET SIZE & FORECAST
- 15.5.3 POST-AUTHORIZATION: GEOGRAPHY SEGMENTATION
16 GEOGRAPHY
- 16.1 MARKET SNAPSHOT & GROWTH ENGINE
- 16.2 GEOGRAPHIC OVERVIEW
17 NORTH AMERICA
- 17.1 MARKET OVERVIEW
- 17.2 MARKET SIZE & FORECAST
- 17.2.1 NORTH AMERICA: PRODUCT SEGMENTATION
- 17.2.2 NORTH AMERICA: COMPANY SIZE SEGMENTATION
- 17.2.3 NORTH AMERICA: END-USER SEGMENTATION
- 17.2.4 NORTH AMERICA: SERVICE TYPE SEGMENTATION
- 17.3 KEY COUNTRIES
- 17.3.1 US: MARKET SIZE & FORECAST
- 17.3.2 CANADA: MARKET SIZE & FORECAST
18 EUROPE
- 18.1 MARKET OVERVIEW
- 18.2 MARKET SIZE & FORECAST
- 18.2.1 EUROPE: PRODUCT SEGMENTATION
- 18.2.2 EUROPE: COMPANY SIZE SEGMENTATION
- 18.2.3 EUROPE: END-USER SEGMENTATION
- 18.2.4 EUROPE: SERVICE TYPE SEGMENTATION
- 18.3 KEY COUNTRIES
- 18.3.1 GERMANY: MARKET SIZE & FORECAST
- 18.3.2 FRANCE: MARKET SIZE & FORECAST
- 18.3.3 UK: MARKET SIZE & FORECAST
- 18.3.4 ITALY: MARKET SIZE & FORECAST
- 18.3.5 SPAIN: MARKET SIZE & FORECAST
19 APAC
- 19.1 MARKET OVERVIEW
- 19.2 MARKET SIZE & FORECAST
- 19.2.1 APAC: PRODUCT SEGMENTATION
- 19.2.2 APAC: COMPANY SIZE SEGMENTATION
- 19.2.3 APAC: END-USER SEGMENTATION
- 19.2.4 APAC: SERVICE TYPE SEGMENTATION
- 19.3 KEY COUNTRIES
- 19.3.1 JAPAN: MARKET SIZE & FORECAST
- 19.3.2 CHINA: MARKET SIZE & FORECAST
- 19.3.3 SOUTH KOREA: MARKET SIZE & FORECAST
- 19.3.4 INDIA: MARKET SIZE & FORECAST
- 19.3.5 AUSTRALIA: MARKET SIZE & FORECAST
20 LATIN AMERICA
- 20.1 MARKET OVERVIEW
- 20.2 MARKET SIZE & FORECAST
- 20.2.1 LATIN AMERICA: PRODUCT SEGMENTATION
- 20.2.2 LATIN AMERICA: COMPANY SIZE SEGMENTATION
- 20.2.3 LATIN AMERICA: END-USER SEGMENTATION
- 20.2.4 LATIN AMERICA: SERVICE TYPE SEGMENTATION
- 20.3 KEY COUNTRIES
- 20.3.1 BRAZIL: MARKET SIZE & FORECAST
- 20.3.2 MEXICO: MARKET SIZE & FORECAST
- 20.3.3 ARGENTINA: MARKET SIZE & FORECAST
21 MIDDLE EAST & AFRICA
- 21.1 MARKET OVERVIEW
- 21.2 MARKET SIZE & FORECAST
- 21.2.1 MIDDLE EAST & AFRICA: PRODUCT SEGMENTATION
- 21.2.3 MIDDLE EAST & AFRICA: COMPANY SIZE SEGMENTATION
- 21.2.4 MIDDLE EAST & AFRICA: END-USER SEGMENTATION
- 21.2.6 MIDDLE EAST & AFRICA: SERVICE TYPE SEGMENTATION
- 21.3 KEY COUNTRIES
- 21.3.1 TURKEY: MARKET SIZE & FORECAST
- 21.3.2 SAUDI ARABIA: MARKET SIZE & FORECAST
- 21.3.3 SOUTH AFRICA: MARKET SIZE & FORECAST
- 21.3.4 UAE: MARKET SIZE & FORECAST
22 COMPETITIVE LANDSCAPE
- 22.1 COMPETITION OVERVIEW
- 22.2 MARKET SHARE ANALYSIS
- 22.2.1 FREYR
- 22.2.2 GENPACT
- 22.2.3 ICON
- 22.2.4 IQVIA
- 22.2.5 LABCORP DRUG DEVELOPMENT
- 22.2.6 MEDPACE
- 22.2.7 PPD
- 22.2.8 PAREXEL
23 KEY COMPANY PROFILES
- 23.1 GENPACT
- 23.1.1 BUSINESS OVERVIEW
- 23.1.2 SERVICE OFFERINGS
- 23.1.3 KEY STRATEGIES
- 23.1.4 KEY STRENGTHS
- 23.1.5 KEY OPPORTUNITIES
- 23.2 LABCORP DRUG DEVELOPMENT
- 23.2.1 BUSINESS OVERVIEW
- 23.2.2 SERVICE OFFERINGS
- 23.2.3 KEY STRATEGIES
- 23.2.4 KEY STRENGTHS
- 23.2.5 KEY OPPORTUNITIES
- 23.3 FREYR
- 23.3.1 BUSINESS OVERVIEW
- 23.3.2 SERVICE OFFERINGS
- 23.3.3 KEY STRATEGIES
- 23.3.4 KEY STRENGTHS
- 23.3.5 KEY OPPORTUNITIES
- 23.4 ICON
- 23.4.1 BUSINESS OVERVIEW
- 23.4.2 SERVICE OFFERINGS
- 23.4.3 KEY STRATEGIES
- 23.4.4 KEY STRENGTHS
- 23.4.5 KEY OPPORTUNITIES
- 23.5 IQVIA
- 23.5.1 BUSINESS OVERVIEW
- 23.5.2 SERVICE OFFERINGS
- 23.5.3 KEY STRATEGIES
- 23.5.4 KEY STRENGTHS
- 23.5.5 KEY OPPORTUNITIES
- 23.6 MEDPACE
- 23.6.1 BUSINESS OVERVIEW
- 23.6.2 SERVICE OFFERINGS
- 23.6.3 KEY STRATEGIES
- 23.6.4 KEY STRENGTHS
- 23.6.5 KEY OPPORTUNITIES
- 23.7 PAREXEL INTERNATIONAL
- 23.7.1 BUSINESS OVERVIEW
- 23.7.2 SERVICE OFFERINGS
- 23.7.3 KEY STRATEGIES
- 23.7.4 KEY STRENGTHS
- 23.7.5 KEY OPPORTUNITIES
- 23.8 PPD
- 23.8.1 BUSINESS OVERVIEW
- 23.8.2 SERVICE OFFERINGS
- 23.8.3 KEY STRATEGIES
- 23.8.4 KEY STRENGTHS
- 23.8.5 KEY OPPORTUNITIES
24 OTHER PROMINENT VENDORS
- 24.1 ACCENTURE
- 24.1.1 BUSINESS OVERVIEW
- 24.1.2 SERVICE OFFERINGS
- 24.2 BLUEREG
- 24.2.1 BUSINESS OVERVIEW
- 24.2.2 SERVICE OFFERINGS
- 24.3 INTERTEK GROUP
- 24.3.1 BUSINESS OVERVIEW
- 24.3.2 SERVICE OFFERINGS
- 24.4 LACHMAN CONSULTANTS
- 24.4.1 BUSINESS OVERVIEW
- 24.4.2 SERVICE OFFERINGS
- 24.5 NDA GROUP
- 24.5.1 BUSINESS OVERVIEW
- 24.5.2 SERVICE OFFERINGS
- 24.6 PROPHARMA GROUP
- 24.6.1 BUSINESS OVERVIEW
- 24.6.2 SERVICE OFFERINGS
- 24.7 PHARMALEX
- 24.7.1 BUSINESS OVERVIEW
- 24.7.2 SERVICE OFFERINGS
- 24.8 PHARMEXON
- 24.8.1 BUSINESS OVERVIEW
- 24.8.2 SERVICE OFFERINGS
- 24.9 PROMEDICA INTERNATIONAL
- 24.9.1 BUSINESS OVERVIEW
- 24.9.2 SERVICE OFFERINGS
- 24.10 CRITERIUM
- 24.10.1 BUSINESS OVERVIEW
- 24.10.2 SERVICE OFFERINGS
- 24.11 DICENTRA
- 24.11.1 BUSINESS OVERVIEW
- 24.11.2 SERVICE OFFERINGS
- 24.12 NUVENTRA PHARMA SCIENCES
- 24.12.1 BUSINESS OVERVIEW
- 24.12.2 SERVICE OFFERINGS
- 24.13 PHARMALEAF
- 24.13.1 BUSINESS OVERVIEW
- 24.13.2 SERVICE OFFERINGS
- 24.14 MAVEN REGULATORY SOLUTIONS
- 24.14.1 BUSINESS OVERVIEW
- 24.14.2 SERVICE OFFERINGS
- 24.15 GLOBAL REGULATORY PARTNERS
- 24.15.1 BUSINESS OVERVIEW
- 24.15.2 SERVICE OFFERINGS
- 24.16 SOFPROMED
- 24.16.1 BUSINESS OVERVIEW
- 24.16.2 SERVICE OFFERINGS
- 24.17 CHARLES RIVER LABORATORIES
- 24.17.1 BUSINESS OVERVIEW
- 24.17.2 SERVICE OFFERINGS
- 24.18 CAMBRIDGE REGULATORY SERVICES
- 24.18.1 BUSINESS OVERVIEW
- 24.18.2 SERVICE OFFERINGS
- 24.19 APC GROUP
- 24.19.1 BUSINESS OVERVIEW
- 24.19.2 SERVICE OFFERINGS
- 24.20 REAL REGULATORY
- 24.20.1 BUSINESS OVERVIEW
- 24.20.2 SERVICE OFFERINGS
- 24.21 VOISIN CONSULTING LIFE SCIENCES (VCLS)
- 24.21.1 BUSINESS OVERVIEW
- 24.21.2 SERVICE OFFERINGS
- 24.22 REGULATORY PHARMA NET
- 24.22.1 BUSINESS OVERVIEW
- 24.22.2 SERVICE OFFERINGS
- 24.23 BIOMAPAS
- 24.23.1 BUSINESS OVERVIEW
- 24.23.2 SERVICE OFFERINGS
- 24.24 REGENOLD
- 24.24.1 BUSINESS OVERVIEW
- 24.24.2 SERVICE OFFERINGS
25 REPORT SUMMARY
- 25.1 KEY TAKEAWAYS
- 25.2 STRATEGIC RECOMMENDATIONS
26 QUANTITATIVE SUMMARY
- 26.1 MARKET BY PRODUCT
- 26.1.1 NORTH AMERICA: PRODUCT SEGMENTATION
- 26.1.2 EUROPE: PRODUCT SEGMENTATION
- 26.1.3 APAC: PRODUCT SEGMENTATION
- 26.1.4 LATIN AMERICA: PRODUCT SEGMENTATION
- 26.1.5 MIDDLE EAST & AFRICA: PRODUCT SEGMENTATION
- 26.2 MARKET BY COMPANY SIZE
- 26.2.1 NORTH AMERICA: COMPANY SIZE SEGMENTATION
- 26.2.2 EUROPE: COMPANY SIZE SEGMENTATION
- 26.2.3 APAC: COMPANY SIZE SEGMENTATION
- 26.2.4 LATIN AMERICA: COMPANY SIZE SEGMENTATION
- 26.2.5 MIDDLE EAST & AFRICA: COMPANY SIZE SEGMENTATION
- 26.3 MARKET BY END-USER
- 26.3.1 NORTH AMERICA: END-USER SEGMENTATION
- 26.3.2 EUROPE: END-USER SEGMENTATION
- 26.3.3 APAC: END-USER SEGMENTATION
- 26.3.4 LATIN AMERICA: END-USER SEGMENTATION
- 26.3.5 MIDDLE EAST & AFRICA: END-USER SEGMENTATION
- 26.4 MARKET BY SERVICE TYPE
- 26.4.1 NORTH AMERICA: SERVICE TYPE SEGMENTATION
- 26.4.2 EUROPE: SERVICE TYPE SEGMENTATION
- 26.4.3 APAC: SERVICE TYPE SEGMENTATION
- 26.4.4 LATIN AMERICA: SERVICE TYPE SEGMENTATION
- 26.4.5 MIDDLE EAST & AFRICA: SERVICE TYPE SEGMENTATION
- 26.5 MARKET BY GEOGRAPHY
- 26.5.1 DRUGS: GEOGRAPHY SEGMENTATION
- 26.5.2 BIOLOGICS: GEOGRAPHY SEGMENTATION
- 26.5.3 MEDICAL DEVICES: GEOGRAPHY SEGMENTATION
- 26.5.4 OTHERS: GEOGRAPHY SEGMENTATION
- 26.5.5 SMALL & MID-SIZED COMPANIES: GEOGRAPHY SEGMENTATION
- 26.5.6 LARGE-SIZED COMPANIES: GEOGRAPHY SEGMENTATION
- 26.5.7 PHARMA & BIOTECH COMPANIES: GEOGRAPHY SEGMENTATION
- 26.5.8 MEDICAL DEVICE COMPANIES: GEOGRAPHY SEGMENTATION
- 26.5.9 OTHER COMPANIES: GEOGRAPHY SEGMENTATION
- 26.5.10 PRE-AUTHORIZATION: GEOGRAPHY SEGMENTATION
- 26.5.11 MARKETING AUTHORIZATION: GEOGRAPHY SEGMENTATION
- 26.5.12 POST-AUTHORIZATION: GEOGRAPHY SEGMENTATION
27 APPENDIX