Over 400 companies claim that they can hold the needed expertise to provide regulatory matters management-re

Greater than 130 medical devices were authorized by the Food and drug administration since The month of january 2018, while several are presently being evaluated across greater than 9,500 (active) numerous studies, worldwide. Despite the fact that technical innovation has allowed the introduction of a number of versatile medical devices, product approval, given stringent regulatory standards, continues to be an issue.

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The USD 820 million (by 2030) financial chance inside the contract regulatory matters-management services marketplace for medical devices continues to be examined over the following segments:

•           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 Matters Service

•           Pharmacies GAP-Analysis

•           Pharmacies An Attorney

•           Pharmacies Notified Body Selection

•           Product Labelling-related Services

•           Product Registration and Medical 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-Off-shore and World

Anything Regulatory Matters-Management Marketplace for Medical Devices, 2019-2030 report features the next companies, which we identified to become key players within this domain:

•           CTI Medical Trial and Talking to Services

•           CROMSOURCE

•           ICON

•           Intertek

•           Medpace

•           MIC Medical

•           North American Science Associates (NAMSA)

•           Parexel

•           PharmaLex

•           Premier Research

•           Société Générale de Surveillance (SGS)

•           Underwriters Laboratory (UL)

Table of Contents


2. Executive Summary



3.Role of Regulatory Matters in Medical Device Logistics

4.Regulatory and Reimbursement Landscape for Medical Devices

5.Competitive Landscape

6.Company Profiles

7.Competitive Benchmarking

8.Help guide to Regulatory Outsourcing Models

9.Medical Device Regulatory Matters: Key Performance Indicators

10.Market Forecast


12.Survey Insights

13.Executive Insights

1.Appendix 1: Tabulated Data

1.Appendix 2: Listing of Organizations and companies

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