{"id":67331,"date":"2024-11-27T19:00:57","date_gmt":"2024-11-27T13:30:57","guid":{"rendered":"https:\/\/corpbiz.io\/learning\/?p=67331"},"modified":"2026-03-19T17:27:38","modified_gmt":"2026-03-19T11:57:38","slug":"bis-sets-indian-standards-for-214-medical-devices-by-2025","status":"publish","type":"post","link":"https:\/\/corpbiz.io\/learning\/bis-sets-indian-standards-for-214-medical-devices-by-2025\/","title":{"rendered":"BIS Sets Indian Standards for 214 Medical Devices by 2025"},"content":{"rendered":"\n<p>An important announcement has been made by the BIS to develop standards for 214 critical medical devices.&nbsp; The goal is to complete the work by December 2025. The standards being created are a part of the National Medical Device Policy,2023 which aims to improve the medical device industry of India globally. The prioritized devices include septal closure devices (which are used in heart surgeries), plasma sterilizers (for cleaning medical instruments), and phototherapy machines (for treating skin conditions).<\/p>\n\n\n\n<p>In collaboration with the Department of Pharmaceuticals, these devices were selected to meet the increasing demand for standardization in the medical industry.&nbsp;<\/p>\n\n\n\n<p>According to the statement of BIS, they are further focusing on medical products supporting individuals with disabilities. This includes products like therapeutic footwear (which helps people with foot problems), portable ramps (easy access to buildings), braille displays (for the visually impaired), and fall detectors (which prevent accidents for elderly or disabled people). Through the products, it is expected to better the lives of the elderly and people with disabilities.&nbsp;<\/p>\n\n\n\n<div id=\"ez-toc-container\" class=\"ez-toc-v2_0_82_2 counter-hierarchy ez-toc-counter ez-toc-grey ez-toc-container-direction\">\n<div class=\"ez-toc-title-container\">\n<p class=\"ez-toc-title ez-toc-toggle\" style=\"cursor:pointer\">Page Contents<\/p>\n<span class=\"ez-toc-title-toggle\"><a href=\"#\" class=\"ez-toc-pull-right ez-toc-btn ez-toc-btn-xs ez-toc-btn-default ez-toc-toggle\" aria-label=\"Toggle Table of Content\"><span class=\"ez-toc-js-icon-con\"><span class=\"\"><span class=\"eztoc-hide\" style=\"display:none;\">Toggle<\/span><span class=\"ez-toc-icon-toggle-span\"><svg style=\"fill: #999;color:#999\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" class=\"list-377408\" width=\"20px\" height=\"20px\" viewBox=\"0 0 24 24\" fill=\"none\"><path d=\"M6 6H4v2h2V6zm14 0H8v2h12V6zM4 11h2v2H4v-2zm16 0H8v2h12v-2zM4 16h2v2H4v-2zm16 0H8v2h12v-2z\" fill=\"currentColor\"><\/path><\/svg><svg style=\"fill: #999;color:#999\" class=\"arrow-unsorted-368013\" xmlns=\"http:\/\/www.w3.org\/2000\/svg\" width=\"10px\" height=\"10px\" viewBox=\"0 0 24 24\" version=\"1.2\" baseProfile=\"tiny\"><path d=\"M18.2 9.3l-6.2-6.3-6.2 6.3c-.2.2-.3.4-.3.7s.1.5.3.7c.2.2.4.3.7.3h11c.3 0 .5-.1.7-.3.2-.2.3-.5.3-.7s-.1-.5-.3-.7zM5.8 14.7l6.2 6.3 6.2-6.3c.2-.2.3-.5.3-.7s-.1-.5-.3-.7c-.2-.2-.4-.3-.7-.3h-11c-.3 0-.5.1-.7.3-.2.2-.3.5-.3.7s.1.5.3.7z\"\/><\/svg><\/span><\/span><\/span><\/a><\/span><\/div>\n<nav><ul class='ez-toc-list ez-toc-list-level-1 eztoc-toggle-hide-by-default' ><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-1\" href=\"https:\/\/corpbiz.io\/learning\/bis-sets-indian-standards-for-214-medical-devices-by-2025\/#Medical_Devices_Crucial_for_Healthcare\" >Medical Devices Crucial for Healthcare<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-2\" href=\"https:\/\/corpbiz.io\/learning\/bis-sets-indian-standards-for-214-medical-devices-by-2025\/#Talk_To_Expert\" >Talk To Expert<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-3\" href=\"https:\/\/corpbiz.io\/learning\/bis-sets-indian-standards-for-214-medical-devices-by-2025\/#BIS_Sets_Indian_Standards_for_214_Medical_Devices_by_2025\" >BIS Sets Indian Standards for 214 Medical Devices by 2025<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-4\" href=\"https:\/\/corpbiz.io\/learning\/bis-sets-indian-standards-for-214-medical-devices-by-2025\/#Key_Indian_Standards_Developed_by_BIS\" >Key Indian Standards Developed by BIS<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-5\" href=\"https:\/\/corpbiz.io\/learning\/bis-sets-indian-standards-for-214-medical-devices-by-2025\/#What_is_BIS_and_Its_Role_in_Standardization\" >What is BIS and Its Role in Standardization?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-6\" href=\"https:\/\/corpbiz.io\/learning\/bis-sets-indian-standards-for-214-medical-devices-by-2025\/#What_Does_BIS_Do\" >What Does BIS Do?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-7\" href=\"https:\/\/corpbiz.io\/learning\/bis-sets-indian-standards-for-214-medical-devices-by-2025\/#Why_Set_Standards_for_Medical_Devices\" >Why Set Standards for Medical Devices?<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-8\" href=\"https:\/\/corpbiz.io\/learning\/bis-sets-indian-standards-for-214-medical-devices-by-2025\/#In_a_Nutshell\" >In a Nutshell<\/a><\/li><li class='ez-toc-page-1 ez-toc-heading-level-2'><a class=\"ez-toc-link ez-toc-heading-9\" href=\"https:\/\/corpbiz.io\/learning\/bis-sets-indian-standards-for-214-medical-devices-by-2025\/#Frequently_Asked_Questions\" >Frequently Asked Questions<\/a><\/li><\/ul><\/nav><\/div>\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Medical_Devices_Crucial_for_Healthcare\"><\/span>Medical Devices Crucial for Healthcare<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>BIS, to date, has published over 1,700 standards for the medical sector covering a wide variety of medical specialties like cardiology (heart care), neurology (brain health), orthopaedics (bone and joint health), and ophthalmology (eye care). Around 1200 of the standards focus on the medical devices crucial for healthcare. This includes:&nbsp;<\/p>\n\n\n\n<ul>\n<li><strong>Life-saving devices:<\/strong> Cardiac pacemakers, heart valves, ventilators, and haemodialysis machines.<\/li>\n\n\n\n<li><strong>Advanced diagnostic tools:<\/strong> X-ray machines, CT scanners, MRI systems, and blood glucose monitors<\/li>\n\n\n\n<li><strong>Assistive technology:<\/strong> Hearing aids, wheelchairs, Jaipur Foot, and tactile pathways<\/li>\n<\/ul>\n\n\n\n<p>Ministry talked about the number of standards set for different medical fields out of which dentistry has the maximum standards with 249. Followed by Surgical disposables (surgery tools) having 205 rules, Orthopaedics (bones and joints) having 155 rules, Assistive products (tools to help people) having 152 rules, ENT (ear, nose, throat), Gynaecology (women&#8217;s health), and Cardiology (heart) having the least rules: about 70 each. &nbsp;<\/p>\n\n\n\n<p>The standards by BIS help ensure the public that devices are safe, reliable, and perform well. Following the BIS standards, Indian manufacturers can stand out in the competitive global market of medical devices benefiting both the domestic and global health sectors. The initiatives reflect the effort of India to boost the healthcare infrastructure.&nbsp; &nbsp;<\/p>\n\n\n\n<h2><span class=\"ez-toc-section\" id=\"Talk_To_Expert\"><\/span>Talk To Expert<span class=\"ez-toc-section-end\"><\/span><\/h2><div class=\"calling-person blog_cta my-4\"> \n\n  \n\n    <div class=\"row\"> \n\n        <div class=\"col-xs-12 col-sm-12 col-md-12 col-lg-12\"> \n\n            <div class=\"d-flex flex-nowrap\"> \n\n                <div class=\"user-online\"> <img decoding=\"async\" src=\"https:\/\/corpbiz.io\/img\/user.jpg\" alt=\"corpbiz\"> <\/div> \n\n                <div class=\"user-online-details ms-3 align-self-center\"> \n\n                    <h2 class=\"text-white mt-0\"><span class=\"ez-toc-section\" id=\"BIS_Sets_Indian_Standards_for_214_Medical_Devices_by_2025\"><\/span> BIS Sets Indian Standards for 214 Medical Devices by 2025 <span class=\"ez-toc-section-end\"><\/span><\/h2> \n\n                    <p class=\"mt-3\"><i class=\"fa fa-star\"><\/i><i class=\"fa fa-star\"><\/i><i class=\"fa fa-star\"><\/i><i \n\n                            class=\"fa fa-star\"><\/i><i class=\"fa fa-star-half-full\"><\/i><span \n\n                            class=\"ms-2 text-white\">(4.8)<\/span><\/p> \n\n                <\/div> \n\n            <\/div> \n\n          \n\n        <\/div> \n\n     \n\n        <div class=\"col-xs-12 col-sm-12 col-md-12 col-lg-8 mx-auto\"> \n\n            <div class=\"d-flex justify-content-between call-chat\"> <a href=\"tel:919121230280\"> <span>Call Now \n\n            <\/span><img decoding=\"async\" class=\"ms-2\" src=\"https:\/\/corpbiz.io\/admin\/style\/images\/userfiles\/image\/new_call_icon.png\" \n\n                alt=\"Call With \" width=\"32px\"> \n\n        <\/a> <a href=\"https:\/\/api.whatsapp.com\/send?phone=919289379709&#038;text=Hi%20Corpbiz\" target=\"_blank\" rel=\"noopener\"> <span>Chat With Us<\/span><img decoding=\"async\" class=\"ms-2\" \n\n                src=\"https:\/\/corpbiz.io\/img\/chat-with-expert.png\" alt=\"Chat With \" width=\"32px\"> <\/a> <\/div> \n\n        <\/div> \n\n    <\/div> \n\n<\/div>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Key_Indian_Standards_Developed_by_BIS\"><\/span>Key Indian Standards Developed by BIS<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p><strong>Some of the key Indian standards developed by BIS:<\/strong><\/p>\n\n\n\n<ul type=\"1\">\n<li>Cardiac Pacemakers: IS 13450 (Part 2\/Sec 31): 2021<\/li>\n\n\n\n<li>Heart Waves: IS 17840<\/li>\n\n\n\n<li>Hip and Knee Implants: IS 12375<\/li>\n\n\n\n<li>Ventilators: is 13450 (Part2\/Sec12): 2023<\/li>\n\n\n\n<li>Infant Incubators and Radiant Warmers: IS 13450<\/li>\n\n\n\n<li>(Part 2\/Sec 19): 2023 for incubators and IS 13450<\/li>\n\n\n\n<li>Part 2\/Sec 21): 2023 for radiant warmers<\/li>\n\n\n\n<li>Haemodialysis Machines: IS 3450 (Part3\/Sec 16):2019 <\/li>\n\n\n\n<li>Advanced Diagnostic Tools:<br>&#8211; X-ray and CT Machines: IS 7620 (Part 1): 1986<br>&#8211; ECG: Covered under IS 13450 (Part 2\/Sec 25): 2018<br>&#8211; MRI Systems: IS 13450 (Part 2\/Sec 33): 2018<br>&#8211; Ultrasound Devices: 13450 (Part 2\/Sec 37): 2019<\/li>\n\n\n\n<li>Monitoring Devices:<br>&#8211; Blood Pressure Monitors: IS 13450 (Part 2\/Sec 34): 2019<br>&#8211; Blood Glucose Monitors: IS\/ISO 15197: 2013<br>&#8211; Pulse Oximeters: IS\/ISO 80601-2-61:2017<\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"What_is_BIS_and_Its_Role_in_Standardization\"><\/span>What is BIS and Its Role in Standardization?<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>BIS, which stands for Bureau of Indian Standards, is the National Standard Body of India established under the Bureau of Indian Standards Act, 2016. BIS operates under the Ministry of Consumer Affairs, Food and Public Distribution. It is an official body responsible for setting the standard for products and services with quality assurance and extensive certification for compliance.<\/p>\n\n\n\n<p>The main function of BIS is to promote and develop Indian standards in various fields, such as quality, safety, and reliability of products\/services\/systems. BIS plays a key role in maintaining standardization. They construct guidelines on how products and services should be made, tested, and used to ensure their safety, reliability, and good quality. BIS ensures consumer protection and fosters domestic and international trust in Indian products. Besides<strong> <a title=\"CDSCO Online Registration\" href=\"https:\/\/corpbiz.io\/cdsco-registration\">CDSCO registration<\/a><\/strong>, BIS registration also matters for medical devices nowadays.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"What_Does_BIS_Do\"><\/span>What Does BIS Do?<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The activities of the Bureau of Indian Standards are;<\/p>\n\n\n\n<p><strong>Standardization<\/strong>&#8211; BIS formulates and revises national standards concerning specific products and services. Such standards help industries manufacture products that are safe and high in quality as well as fulfill environmental specifications. It will allow consumers to gain faith in the products offered to them.<\/p>\n\n\n\n<p><strong>Certification<\/strong>: The Bureau of Indian Standards (BIS) certifies products so that those products can be proven to stand by certain set standards. An example is that an<strong> <a title=\"ISI Mark Certification\" href=\"https:\/\/corpbiz.io\/isi-mark-certification\">ISI mark<\/a><\/strong> on a product would mean that the product complies with the standards laid down in India.<\/p>\n\n\n\n<p><strong>Consumer Protection<\/strong>: <strong><a title=\"BIS Certification in India\" href=\"https:\/\/corpbiz.io\/bis-registration\">BIS registration<\/a> <\/strong>ensures safety and reliability in medical devices such that users and healthcare professionals do not suffer loss because of using faulty devices. Further, if any product does not meet the expected standards, BIS can withdraw the product from the market to take action to protect consumers.<\/p>\n\n\n\n<p><strong>International Cooperation<\/strong>: BIS works with international organizations such as the International Organization for Standardization (ISO) to ensure that Indian standards for medical devices are in line with international standards. Consequently, this standardization allows Indian manufacturers to compete in the international marketplace and ensures that Indian medical devices gain global acceptance, thus increasing trade and export of Indian medical devices.&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;<\/p>\n\n\n\n<p><strong>Training and Awareness<\/strong>: BIS provides training and awareness programs for <strong><a href=\"https:\/\/corpbiz.io\/medical-device-registration\">medical device manufacturers<\/a><\/strong>, healthcare providers, and even consumers. Awareness programs offer education to the industry on the importance of quality standards and certifications and subsequently help ensure all the stakeholders can work with safe and certified medical devices.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Why_Set_Standards_for_Medical_Devices\"><\/span>Why Set Standards for Medical Devices?<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>For the healthcare system to function smoothly with high-quality tools for medical treatment, setting standards for Medical Devices is important. Here are other reasons for the need for Standardization:<\/p>\n\n\n\n<p><strong>Patient Safety<\/strong>: Medical Devices are to be used directly on patients. It can cause serious harm if not standardized due to its defects, malfunctions, or poor quality. Following the standard makes sure the device is safe and avoids potential risks.<\/p>\n\n\n\n<p><strong>Consistency and Reliability<\/strong>: Standardization ensures that each medical devices meet the requirements and can rely on the product every time safely preventing errors in treatment.<\/p>\n\n\n\n<p><strong>International Alignment and Trade: <\/strong>Standard medical devices are not only essential for domestic health infrastructure but also for international trade. Meeting the standards is important for the import and export of medical devices. Holding to the internationally accepted standards, India can enhance its participation in global health initiatives.<\/p>\n\n\n\n<p><strong>Minimizing Medical Device Failures<\/strong>: Standard calibration procedures, along with routine equipment maintenance, are tools for verifying the performance and accuracy of the medical equipment throughout its lifetime. Thus, the failure risk is reduced.<\/p>\n\n\n\n<p><strong>Innovation And Improvement<\/strong>: These standards allow manufacturers to innovate. It can ensure new devices become safer and more effective. In this regard, companies are free to improve the existing devices or add new devices without negatively affecting their quality or safety.<\/p>\n\n\n\n<p><strong>Transparency and Accountability: <\/strong>Transparency enables all parties, such as producers, regulators, and consumers, to evaluate and understand the quality and reliability of medical devices in a standardized manner. Visibility guarantees the accountability of manufacturers in producing safe and effective products while easing compliance oversight for regulators. Consumers, in turn, get assurance about the products they use.<\/p>\n\n\n\n<p><strong>Economic Growth<\/strong>: Setting standards would build a regulatory environment that would facilitate domestic manufacture and export of India-based medical devices, leading to economic growth.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"In_a_Nutshell\"><\/span>In a Nutshell<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n\n<p>The initiative by the Bureau of Indian Standards, BIS, is a significant step to enhance the development of the medical device sector in India by laying down standards for 214 high-priority medical devices by 2025. These steps would improve patient safety and reliability of medical products while ensuring Indian manufacturers&#8217; global competitiveness. BIS standards would provide not only the safety and performance of medical devices but also mark India as a strong competitor in international medical device markets.<\/p>\n\n\n\n<p>BIS&#8217;s focus on critical device areas, lifesaving devices, diagnostics, and assistive technology devices for persons with disabilities contributes to the improvement of national healthcare infrastructure. These measures collectively are an important strategy for India to enhance the quality of medical devices and ensure their availability in both national and international markets, thus driving economic growth and health for all.<\/p>\n\n\n\n<p>To get expert support in BIS registration without any hassle, visit <a rel=\"noreferrer noopener\" href=\"https:\/\/corpbiz.io\/\" target=\"_blank\">https:\/\/corpbiz.io\/<\/a>.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\"><span class=\"ez-toc-section\" id=\"Frequently_Asked_Questions\"><\/span>Frequently Asked Questions<span class=\"ez-toc-section-end\"><\/span><\/h2>\n\n\n<div class=\"saswp-faq-block-section\"><ol style=\"list-style-type:none\"><li style=\"list-style-type: none\"><h3>What is the Bureau of Indian Standards (BIS)?<\/h3><p class=\"saswp-faq-answer-text\">BIS is a recognized National Standard Body of India that is responsible for developing and modifying standards related to various products and services. The function is to ensure that products are kept safe and reliable, thereby helping to protect consumers. The Bureau is also responsible for the certification of products so that these products are framed according to Indian standards.<\/p><li style=\"list-style-type: none\"><h3>Why BIS develops standards for Medical Devices?<\/h3><p class=\"saswp-faq-answer-text\">The primary purpose of developing a standard for medical devices is to ascertain their safety and reliability for performance in the healthcare sector. Therefore, all medical products must be safe for patients and meet international safety and quality standards. This will help enhance the competitiveness of Indian manufacturers in the world&#039;s medical devices market.<\/p><li style=\"list-style-type: none\"><h3>What are the key medical devices for which the standards are being set by the BIS by 2025?<\/h3><p class=\"saswp-faq-answer-text\">BIS is working towards 214 critical medical devices by the year 2025. This list consists of life-saving devices such as cardiac pacemakers, advanced diagnostic equipment such as CT scanners, and assistive devices for people with disabilities like portable ramps and braille displays. The prime determinant here is the aspect of quality improvement and safety for all these devices.<\/p><li style=\"list-style-type: none\"><h3>In what ways does BIS serve Indian medical devices and promote their competitiveness globally?<\/h3><p class=\"saswp-faq-answer-text\">BIS assists Indian producers in positioning themselves with international market standards and makes their products marketable globally. Certification marks like the ISI mark indicate the product&#039;s reliability by meeting certain quality standards to enhance consumer confidence in Indian medical devices as it promotes exports and international trade in medical products.<\/p><li style=\"list-style-type: none\"><h3>Which devices are prioritized in the BIS standardization initiative?<\/h3><p class=\"saswp-faq-answer-text\">The BIS is targeting lifesaving equipment, including cardiac pacemakers and heart valves, diagnostic machines such as MRI units, and aids for disabilities. These devices directly affect patient care relating to the healthcare architecture. Hence, priorities for addressing issues in the critical sectors are set early.<\/p><li style=\"list-style-type: none\"><h3>What are the specifications for cardiac pacemakers according to BIS?<\/h3><p class=\"saswp-faq-answer-text\">Under BIS, the relevant standards for cardiac pacemakers include IS 13450 (Part 2\/Sec 31): 2021. These standards are meant for the safety, efficacy, and reliability of these devices for maintaining heart rhythm. The certification entity gives an assurance that pacemakers are going to function precisely as intended in real-life healthcare settings.<\/p><li style=\"list-style-type: none\"><h3>Can a medical device be withdrawn from the market for not meeting BIS standards?<\/h3><p class=\"saswp-faq-answer-text\">Yes, any medical device can be withdrawn from the market for not conforming to the BIS standards. The Bureau of Indian Standards is empowered to withdraw any medical device from the market if it does not conform to the set standards. This action is for the protection of consumer interests. As long as the manufacturer keeps conforming to the standards, the manufacturer can enjoy the continuance in the market.<\/p><li style=\"list-style-type: none\"><h3>What kind of obstacles does BIS encounter in the process of standardizing medical devices?<\/h3><p class=\"saswp-faq-answer-text\">It becomes increasingly difficult for standards to keep pace with the fast-changing technological advancements in the medical devices industry over time. Continuous monitoring also needs to be ensured regarding the compliance of all manufacturers in each of the product categories with the relevant standards. Harmonization of national standards at the same time poses another challenge before BIS when it comes to the global scenario.<\/p><\/ul><\/div>\n\n\n<p><strong>Read our blog: <\/strong><a href=\"https:\/\/corpbiz.io\/learning\/cdsco-guidelines-for-medical-devices-in-india\/\">A Guide on CDSCO Guidelines for Medical Devices&nbsp;in India<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>An important announcement has been made by the BIS to develop standards for 214 critical medical devices.&nbsp; The goal is to complete the work by December 2025. The standards being created are a part of the National Medical Device Policy,2023 which aims to improve the medical device industry of India globally. The prioritized devices include [&hellip;]<\/p>\n","protected":false},"author":34,"featured_media":67332,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":[],"categories":[2358,946],"tags":[4524,2805],"acf":{"service_id":"508"},"authorName":"Monisha Chaudhary","authorImageUrl":"https:\/\/corpbiz.io\/learning\/wp-content\/uploads\/2022\/01\/Monisha-Chaudhary-150x150.jpg","authorDescription":"Meet Monisha Chaudhary, a company secretary, and legal content expert with 15+ Years of Industry Experience. With a deep understanding of numerous legal domains, such as intellectual property and regulatory affairs, and decades of expertise in drafting legal blogs, she has consistently delivered informative articles. Her unique writing style has made her gain an immense following among legal researchers, lawyers, and CAs.","postViews":3742,"readingTime":7,"_links":{"self":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/67331"}],"collection":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/users\/34"}],"replies":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/comments?post=67331"}],"version-history":[{"count":5,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/67331\/revisions"}],"predecessor-version":[{"id":71406,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/posts\/67331\/revisions\/71406"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media\/67332"}],"wp:attachment":[{"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/media?parent=67331"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/categories?post=67331"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/corpbiz.io\/learning\/wp-json\/wp\/v2\/tags?post=67331"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}