Over the years, outsourcing has become a popular trend with the medical device industry, allowing innovators to leverage the technical and regulatory expertise of contract service providers in order to expedite time to market
Roots Analysis is pleased to announce the publication of its recent study, titled, “Medical Device CROs for Regulatory Affairs Management Market, 2019-2030.”
The report features a detailed study on the current landscape of contract service providers focused on regulatory affairs management for medical devices. The study features an in-depth analysis, highlighting the capabilities of the various CROs engaged in this domain, across different regions of the globe. Amongst other elements, the report includes:
A detailed review of the current market landscape of the medical devices regulatory affairs outsourcing market, featuring a list of over 400 CROs engaged in this domain.
A detailed discussion on the need for regulatory review / oversight across different stages of the medical devices supply chain, with emphasis on the optimization of the supply chain using upcoming tools / technologies.
An elaborate discussion on the various guidelines established by major regulatory bodies for medical device approval across North America, Europe, Asia-Pacific and rest of the world.
Elaborate profiles of popular players that specialize in offering end-to-end regulatory services for medical devices across key geographies.
A benchmark analysis, highlighting the key focus areas of very small-sized, small-sized, mid-sized and large companies, comparing their existing capabilities within and beyond their respective peer groups.
An elaborate discussion on the various outsourcing business models adopted for regulatory affairs management, along with an insightful Harvey ball analysis of key considerations that need to be assessed by industry stakeholders while selecting a CRO partner.
An analysis highlighting the key performance indicators used by sponsor companies to evaluate service providers that are active in the domain, based on information gathered via secondary research (for top-ten medical device players) and primary research.
A survey analysis featuring inputs solicited from various experts who are directly / indirectly involved in providing regulatory affairs management services to medical device developers.
A detailed market forecast, featuring analysis of the current and projected future opportunity across key market segments (listed below)
Medical Device Class
Class I
Class II
Class III
Therapeutic Area
Cardiovascular Disorders
CNS Disorders
Metabolic Disorders
Oncological Disorders
Ophthalmological Disease
Orthopedic Disorders
Pain Disorders
Respiratory Disorders
Others
Type of Regulatory Affairs Service
Pharmacies GAP-Analysis
Pharmacies Legal Representation
Pharmacies Notified Body Selection
Product Labelling-related Services
Product Registration and Clinical Trial Applications
Regulatory Document Submissions
Regulatory Writing and Publishing
Risk Management-related Services
Technical Dossier Set-up
Vigilance & Medical Device Report
Key Geographical Regions
North America
Europe
Asia-Pacific and Rest of the World
Key companies covered in the report
CTI Clinical Trial and Consulting Services
CROMSOURCE
ICON
Intertek
Medpace
MIC Medical
North American Science Associates (NAMSA)
Parexel
PharmaLex
Premier Research
Société Générale de Surveillance (SGS)
Underwriters Laboratory (UL)
For more information please click on the following link
https://www.rootsanalysis.com/reports/view_document/med-dev-regulatory/282.html
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Contact Information
Roots Analysis Private Limited
Gaurav Chaudhary
+1 (415) 800 3415
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