¼¼°èÀÇ ÀÇ·á±â±â RA ½ÃÀå : ½ÃÀå ±Ô¸ð, Á¡À¯À², µ¿Ç⠺м®(À¯Çüº°, ¼­ºñ½º Á¦°ø¾÷üº°, ¼­ºñ½ºº°, Áö¿ªº°), ºÎ¹®º° ¿¹Ãø(2025-2030³â)
Medical Device Regulatory Affairs Market Size, Share & Trends Analysis Report By Type (Diagnostics, Therapeutics), By Service Provider (In-house, Outsource), By Service, By Region, And Segment Forecasts, 2025 - 2030
»óǰÄÚµå : 1632648
¸®¼­Ä¡»ç : Grand View Research, Inc.
¹ßÇàÀÏ : 2024³â 12¿ù
ÆäÀÌÁö Á¤º¸ : ¿µ¹® 172 Pages
 ¶óÀ̼±½º & °¡°Ý (ºÎ°¡¼¼ º°µµ)
US $ 5,950 £Ü 8,302,000
Unprintable PDF & Excel (Single User License) help
º¸°í¼­ PDF ¹× ¿¢¼¿À» 1Àθ¸ »ç¿ëÇÒ ¼ö ÀÖ´Â ¶óÀ̼±½ºÀÔ´Ï´Ù. ÅØ½ºÆ® µîÀÇ º¹»ç ¹× ºÙ¿©³Ö±â, Àμâ´Â ºÒ°¡´ÉÇÕ´Ï´Ù.
US $ 6,950 £Ü 9,698,000
Printable PDF & Excel (5-User License) help
º¸°í¼­ PDF ¹× ¿¢¼¿À» µ¿ÀÏ ±â¾÷ ³» µ¿ÀÏ ºÎ¼­¿¡¼­ ÃÖ´ë 5¸í±îÁö »ç¿ëÇÒ ¼ö ÀÖ´Â ¶óÀ̼±½ºÀÔ´Ï´Ù. ÅØ½ºÆ® µîÀÇ º¹»ç ¹× ºÙ¿©³Ö±â, Àμâ´Â °¡´ÉÇÕ´Ï´Ù.
US $ 8,950 £Ü 12,488,000
Printable PDF & Excel (Enterprise License) help
º¸°í¼­ ±¸¸Å ±â¾÷ ¹× ±× ÀÚȸ»ç, °ü°è»ç°¡ »ç¿ëÇÒ ¼ö ÀÖ´Â ¶óÀ̼±½ºÀ̸ç, PDF ¹× ¿¢¼¿ ÅØ½ºÆ® µîÀÇ º¹»ç ¹× ºÙ¿©³Ö±â, ÀμⰡ °¡´ÉÇÕ´Ï´Ù.


¤± Add-on °¡´É: °í°´ÀÇ ¿äû¿¡ µû¶ó ÀÏÁ¤ÇÑ ¹üÀ§ ³»¿¡¼­ CustomizationÀÌ °¡´ÉÇÕ´Ï´Ù. ÀÚ¼¼ÇÑ »çÇ×Àº ¹®ÀÇÇØ Áֽñ⠹ٶø´Ï´Ù.

Çѱ۸ñÂ÷

ÀÇ·á±â±â RA ½ÃÀåÀÇ ¼ºÀå°ú µ¿Çâ :

Grand View Research, Inc.ÀÇ ÃֽŠº¸°í¼­¿¡ µû¸£¸é ¼¼°è ÀÇ·á±â±â RA ½ÃÀå ±Ô¸ð´Â 2030³â±îÁö 116¾ï 6,000¸¸ ´Þ·¯¿¡ ´ÞÇϸç, 2025³âºÎÅÍ 2030³â±îÁö CAGRÀº 9.55%¸¦ ³ªÅ¸³¾ °ÍÀ¸·Î ¿¹ÃøµË´Ï´Ù.

AI ¹× ¸Ó½Å·¯´×°ú °°Àº ÀÇ·á±â±âÀÇ ±â¼úÀû Áøº¸, ÈÞ´ë¿ë ¼ÒÇü ±â±â·ÎÀÇ µ¿Çâ Áõ°¡, ÀÇ·á±â±â¿¡ ´ëÇÑ Á¤ºÎÀÇ ¾ö°ÝÇÑ ±ÔÁ¦°¡ ½ÃÀåÀ» °ßÀÎÇϰí ÀÖ½À´Ï´Ù.

ÀÇ·á±â±âÀÇ ±ÔÁ¦´Â ±¤´ëÇÏ°í ºü¸£°Ô º¯È­ÇÏ´Â ºÐ¾ßÀ̸ç, Á¾Á¾ ¹ýÀû °úÁ¦·Î º¹ÀâÇØÁý´Ï´Ù. ÇÑ ±ÔÁ¦ ÇÁ·¹ÀÓ¿öÅ© ³»¿¡¼­µµ ¹ý·ü ¿ë¾î¿Í ±× Á¤ÀÇ´Â ¹Ýµå½Ã ÀϰüµÇÁö´Â ¾Ê½À´Ï´Ù. ±â¼úÀÌ È®´ëµÊ¿¡ µû¶ó ¼ÒÇÁÆ®¿þ¾î, ¸Ó½Å·¯´× ¹× ¾Ë°í¸®ÁòÀº Á¡Á¡ ´õ ¸¹Àº µðÁöÅÐ ÀÇ·á ÀÚ¿ø¿¡ ÇʼöÀûÀÎ ¿ä¼Ò°¡ µÇ°í ÀÖ½À´Ï´Ù. ÀÌ ¶§¹®¿¡ ±ÔÁ¦ ÇÁ·¹ÀÓ¿öÅ©¿¡ ÇØ´çÇÏ´Â ±â±âÀÇ ¼ö°¡ ´Ã¾î³ª »õ·Î¿î °úÁ¦°¡ µÇ°í ÀÖ½À´Ï´Ù.

ÀÇ·á±â±â ±â¾÷Àº »ç¾÷Ȱµ¿À̳ª Áö¿ª¿¡ µû¶ó ´Ù¸¥ ±ÔÁ¦¿ä°ÇÀÇ Áö¼ÓÀûÀÎ º¯È­¸¦ ´Ù·ç¾î¾ß ÇÕ´Ï´Ù. º¯È­ÇÏ´Â ±ÔÁ¦ ¿ä°Ç¿¡ ´ëÇÑ ±ÔÁ¤ Áؼö À§¹ÝÀº ¹úÄ¢°ú Áö¿¬À» ÃÊ·¡ÇÏ¿© ¼öÀÍ ¼Õ½Ç·Î À̾îÁú ¼ö ÀÖ½À´Ï´Ù. Genpact°¡ ÁÖÃÖÇÑ Á¶»ç¿¡ µû¸£¸é »ý¸í°úÇÐ ¾÷°èÀÇ °æ¿µ ÀÓ¿øÀÇ 72.0%°¡ ¹ý±Ô Áؼö¸¦ Á÷¸éÇÏ´Â °úÁ¦ÀÇ »óÀ§ 3°¡Áö Áß Çϳª·Î »ý°¢Çϰí ÀÖ½À´Ï´Ù. ÀÌ·¯ÇÑ ¿äÀÎÀ¸·Î ÀÎÇØ ÀÌ·¯ÇÑ ¼­ºñ½º¿¡ ´ëÇÑ ¼ö¿ä°¡ ´õ¿í ³ô¾ÆÁú °ÍÀ¸·Î ¿¹»óµË´Ï´Ù.

¼¼°è °ø°ø ±â°üÀÌ ÀÇ·á ¿¬±¸ °³¹ßÀ» °³¼±Çϱâ À§ÇØ ÀÚ±ÝÀ» Á¦°øÇÕ´Ï´Ù. ¿¹¸¦ µé¾î, 2022³â 3¿ù¿¡´Â Áø´Ü ¹× Ä¡·á¿Í °ü·ÃµÈ NHS ÁÖµµ °Ç°­ ¿¬±¸¸¦ Áö¿øÇϱâ À§ÇØ ¿µ±¹ Á¤ºÎ·ÎºÎÅÍ 1¾ï 8,800¸¸ ´Þ·¯¸¦ ÃʰúÇÏ´Â ÀÚ±ÝÀÌ Á¦°øµÇ¾ú½À´Ï´Ù. ¾ÕÀ¸·Î ÀÌ·¯ÇÑ ÅõÀÚ·Î »õ·Î¿î ÀÇ·á±â±â Ãâ½Ã°¡ Áõ°¡Çϰí ÀÇ·á±â±â ±ÔÁ¦ ¼­ºñ½º ±âȸ°¡ âÃâµÉ °ÍÀ¸·Î ±â´ëµË´Ï´Ù. ÀÌ·¯ÇÑ È°µ¿Àº ¿¹Ãø ±â°£ µ¿¾È ½ÃÀåÀ» Áö¿øÇÒ °ÍÀ¸·Î ±â´ëµË´Ï´Ù.

ÀÇ·á±â±â RA ½ÃÀå : ºÐ¼® °³¿ä

¸ñÂ÷

Á¦1Àå ºÐ¼® ¹æ¹ý¡¤¹üÀ§

Á¦2Àå ÁÖ¿ä ¿ä¾à

Á¦3Àå ÀÇ·á±â±â RA ½ÃÀå : º¯µ¿ ¿äÀΡ¤°æÇ⡤¹üÀ§

Á¦4Àå ÀÇ·á±â±â RA ½ÃÀå : ¼­ºñ½ºº° ÃßÁ¤°ú µ¿Ç⠺м®

Á¦5Àå ÀÇ·á±â±â RA ½ÃÀå : À¯Çüº° ÃßÁ¤°ú µ¿Ç⠺м®

Á¦6Àå ÀÇ·á±â±â RA ½ÃÀå : ¼­ºñ½º Á¦°ø¾÷üº° ÃßÁ¤ ¹× µ¿Ç⠺м®

Á¦7Àå ÀÇ·á±â±â RA ½ÃÀå : Áö¿ªº° ÃßÁ¤°ú µ¿Ç⠺м®

Á¦8Àå °æÀï ±¸µµ

JHS
¿µ¹® ¸ñÂ÷

¿µ¹®¸ñÂ÷

Medical Device Regulatory Affairs Market Growth & Trends:

The global medical device regulatory affairs market size is estimated to reach USD 11.66 billion by 2030, registering to grow at a CAGR of 9.55% from 2025 to 2030 according to a new report by Grand View Research, Inc. Technological advancements in medical devices, such as AI and machine learning, increasing trends toward portable and smaller devices, and strict government regulations for medical devices are driving the market.

Medical equipment regulation is a vast and rapidly changing field that is often complicated by legal challenges. Even within one regulatory framework, legal terms and their definitions are not always consistent. As technology expands, software, machine learning, and algorithms become essential component of an increasing number of digital health resources. This presents new challenges as an increasing number of instruments fall under the regulatory framework.

Medical device companies have to deal with continuous changes in regulatory requirements, which can differ based on business activities and geographies. Noncompliance with the changing regulatory requirements can result in penalties and delays, which may lead to a loss of revenue. According to a survey sponsored by Genpact, 72.0% of executives from the life sciences industry consider regulatory compliance to be one of the top three challenges they face. Such factors are expected to support the demand for these services further.

Public organizations worldwide are providing funding to improve healthcare R&D. For instance, in March 2022, over USD 188.0 million was funded by the U.K. government to support NHS-led health research pertaining to diagnostics and treatments. Such investments in the future are expected to increase the number of new medical device launches, thus creating opportunities for medical device regulatory services. Such activities are expected to support the market in the forecasted period.

Medical Device Regulatory Affairs Market Report Highlights:

Table of Contents

Chapter 1. Research Methodology and Scope

Chapter 2. Executive Summary

Chapter 3. Medical Device Regulatory Affairs Market Variables, Trends & Scope

Chapter 4. Medical Device Regulatory Affairs Market: Services Estimates & Trend Analysis

Chapter 5. Medical Device Regulatory Affairs Market: Type Estimates & Trend Analysis

Chapter 6. Medical Device Regulatory Affairs Market: Service Provider Estimates & Trend Analysis

Chapter 7. Medical Device Regulatory Affairs Market: Regional Estimates & Trend Analysis

Chapter 8. Competitive Landscape

(ÁÖ)±Û·Î¹úÀÎÆ÷¸ÞÀÌ¼Ç 02-2025-2992 kr-info@giikorea.co.kr
¨Ï Copyright Global Information, Inc. All rights reserved.
PC¹öÀü º¸±â