Market revenue in 2023 | USD 291.9 million |
Market revenue in 2030 | USD 433.3 million |
Growth rate | 5.8% (CAGR from 2023 to 2030) |
Largest segment | Product registration & clinical trial applications |
Fastest growing segment | Legal representation |
Historical data | 2018 - 2022 |
Base year | 2023 |
Forecast period | 2024 - 2030 |
Quantitative units | Revenue in USD million |
Market segmentation | Regulatory consulting, Legal representation, Regulatory writing & publishing, Product registration & clinical trial applications, Regulatory Submissions, Regulatory Operations, Other services |
Key market players worldwide | Genpact Ltd, Criterium Inc., Promedica International, Wuxi AppTec Co Ltd, Medpace Holdings Inc, Charles River Laboratories International Inc, Icon PLC, Labcorp Drug Development, FREYR Battery Inc, Cencora Inc, Pharmexon, QVigilance, BlueReg Group, ZEINCRO Group |
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The databook is designed to serve as a comprehensive guide to navigating this sector. The databook focuses on market statistics denoted in the form of revenue and y-o-y growth and CAGR across the globe and regions. A detailed competitive and opportunity analyses related to regulatory affairs outsourcing market will help companies and investors design strategic landscapes.
Product registration & clinical trial applications was the largest segment with a revenue share of 25.97% in 2023. Horizon Databook has segmented the Germany regulatory affairs outsourcing market based on regulatory consulting, legal representation, regulatory writing & publishing, product registration & clinical trial applications, regulatory submissions, regulatory operations, other services covering the revenue growth of each sub-segment from 2018 to 2030.
Germany is one of the largest pharmaceutical markets in the world after the U.S., Japan, and France according to a report by Deloitte and this is one of the major factors responsible for the high demand for regulatory services.
Presence of skilled and experienced workforce is also one of the primary factors expected to drive the Regulatory affairs outsourcing market in Germany as productivity rates are 10% higher than the average of EU15 countries.
The Federal Institute for Drug and Medical Devices and PaulEhrlich-Institut are the two executive agencies under Ministry of Health, which regulate the process of drug development from clinical trial application to post market approvals.
Horizon Databook provides a detailed overview of country-level data and insights on the Germany regulatory affairs outsourcing market , including forecasts for subscribers. This country databook contains high-level insights into Germany regulatory affairs outsourcing market from 2018 to 2030, including revenue numbers, major trends, and company profiles.
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