MedDev Experts

29/06/2025

MD 15 Licese by CDSCO🔍 Navigating the MD-15 license maze? It's not just paperwork—it's your ticket to legally manufacturing Class C & D medical devices in India.

Under the Medical Device Rules 2017, this CDSCO certification isn't optional—it's MANDATORY. And for good reason: it ensures your products meet rigorous safety standards that protect patients.

The 5-year validity gives you stability, but only if you get through the application process first. Documentation headaches keeping you up at night?

Proper compliance isn't just about checking boxes—it's about accelerating your time-to-market while maintaining quality.

What's your biggest MD-15 challenge? Drop it below!

29/06/2025

🇮🇳 ALERT: India's medical device regulations just got a major overhaul!

Thinking of launching your device in the Indian market? The CDSCO has completely transformed the registration process with:

✅ New 4-tier risk classification system
✅ Mandatory SUGAM portal submissions
✅ On-site inspections for higher-risk devices
✅ Risk-based documentation requirements

⏰ Pro tip: Start your registration journey 6-9 months BEFORE your planned launch date. We've seen companies lose millions in revenue due to regulatory delays!

Curious about your specific device requirements? Let's solve your compliance puzzle together - drop your questions below!

26/08/2024

Medical Device Turnkey consultant

Need a Turnkey Consultants for Medical Device or IVD project? MedDev Experts offers expert guidance, fast-tracking your product to market. Contact Now!

26/08/2024

Turnkey consultant for pharmaceutical projects in India

Looking for a reliable pharmaceutical turnkey project consultancy in India? MedDev Experts offers complete solutions from planning to ex*****on. Contact us Now!

28/11/2023

CE Marking Certification Services in India by MedDev Experts

Empower your medical device’s global reach with our expert CE Marking Certification Services in India. MedDev Experts specializes in streamlining EU market access through meticulous processes, from gap analysis to crafting precise Technical Files.

Our expert guidance ensures seamless compliance, navigating complexities to assure your medical devices’ successful market entry. Contact MedDev Experts today and embark on a streamlined path to CE Marking Certification.

https://medicaldevicelicense.com/ce-marking-certification-services-india/

EU Market Access: CE Marking Certification for Medical Devices. Technical File, Gap Analysis, Expert Guidance, Seamless Process. Contact MedDev Experts Now!

28/11/2023

Getting your medical devices registered in Saudi Arabia can be tricky, especially when putting together the detailed technical file needed by the Saudi Food and Drug Authority (SFDA). But with our ready-to-use Technical File Template for Medical Devices, you can make the process much simpler and get your devices registered smoothly in Saudi Arabia.

https://medicaldevicelicense.com/technical-file-template-for-saudi-fda/

Get Complete Technical File Template and Effortlessly Register Your Medical Devices in Saudi Arabia. Contact Now to Get Ready-to-Use Technical Files Templates

28/09/2023

Social Accountability SA 8000 Certification in Baddi, India

If you are interested in getting SA 8000 certified in India, please contact us today. We would be happy to help you through the process. Our dedicated team is here to answer your questions, provide guidance, and support you throughout the certification process.

Social Accountability SA 8000 Certification in Baddi, India: Get certified and demonstrate your commitment to workers' rights and well-being. Contact Us Today!

28/09/2023

Best BIS Certification Consultant in Baddi, India | BIS Mark

Leading BIS Certification Consultant in Baddi, India. We provide Consultancy for BIS Marking, Product Certification, BIS Registration, & Conformity Assessments
The Bureau of Indian Standards (BIS) is a statutory body responsible for establishing standards for products. The BIS Mark is a certification mark that is awarded to products that meet the quality and safety standards set by the BIS.

BIS Certification is compulsory for certain products in India, such as electrical appliances, food products, and medical devices. It is also recommended for other products, as it is a mark of quality and safety that is recognized by consumers.

If you are interested in getting BIS Marking, Product Certification, BIS Registration, and Conformity Assessments, please contact us today. We would be happy to help you through the process. Our dedicated team is here to answer your questions, provide guidance, and support you throughout the registration process.

https://medicaldevicelicense.com/bis-certification-consultant-in-baddi/

Leading BIS Certification Consultant in Baddi, India. We provide Consultancy for BIS Marking, Product Certification, BIS Registration, & Conformity Assessments

25/09/2023

CDSCO License for Self-Testing IVDs in India

Are you a manufacturer or importer of Self-Testing IVDs? The self-testing kits and regents are categorized as in-vitro diagnostic medical devices (IVDs) and are regulated by the Medical Device Rules, 2017.

To manufacture, import, sell, or distribute self-testing IVDs in India, you need a medical device license (MD 5, MD 9, MD 15, or MD 42). This applies to all self-testing kits including Human Chorionic Gonadotropin (hCG), Luteinizing Hormone, Glucose, Glycosylated hemoglobinor its variants, Cholesterol, Follicle Stimulating Hormone (FSH) and Other In-Vitro Diagnostic Medical Devices for Self-Testing.

https://medicaldevicelicense.com/cdsco-license-for-self-testing-ivds/

Fastest CDSCO License and Registration for Self-Testing IVDs in India | Get Your MD 5 and MD 9 License for In-Vitro Diagnostic Medical Devices.

25/09/2023

CDSCO Import license Consultant for Medical Devices

MedDev Experts is the #1 CDSCO Import License Consultant in India. MedDev Experts helps medical device importers obtain the necessary import licenses from the CDSCO. We provide guidance and assistance throughout the application process, from reviewing the required documentation to submitting the application and following up with the CDSCO.

MedDev Experts helps importers who are new to the Indian market or who are unfamiliar with the CDSCO’s complex import regulations. By working with us, importers can increase their chances of having their import license applications approved quickly and efficiently.

Get your CDSCO import license for medical devices quickly and easily with the help of our #1 consultant MedDev Experts. Contact us today for free consultation.

25/09/2023

Best MDR Authorized Agent Service in India for Medical Devices

Welcome to MedDev Experts: Your Trusted MDR Authorized Agent in India

Are you a foreign manufacturer seeking to introduce your cutting-edge medical devices to the thriving healthcare market of India? Look no further than MedDev Experts, your dedicated partner for MDR Authorized Agent Services.

MedDev Experts is a leading provider of MDR Authorized Agent Service in India for medical devices. We help foreign manufacturers to market their products in India by taking care of all the regulatory requirements, including product registration, import licensing, and post-market compliance.

Our team of experienced regulatory experts has a deep understanding of the Indian medical device regulatory landscape and can help you to navigate the complex process of bringing your products to market.

Why You Need an Authorized Agent in India?
In order to market their medical devices in India, foreign manufacturers who do not have a physical presence in the country are required to designate an Authorized Agent. This Authorized Agent plays a pivotal role in ensuring compliance with Indian regulatory standards and to register the devices with the licensing authority of India the Central Drugs Standard Control Organisation (CDSCO).

https://medicaldevicelicense.com/mdr-authorized-agent-service-in-india/

MedDev Experts provides MDR Authorized Agent Service in India for medical devices. We help foreign manufacturers to market their products in India. Contact Now!

25/09/2023

Social Accountability SA 8000 Certification in Baddi, India

Welcome to MedDev Experts, One of the Best SA 8000 Certification Consultant in Baddi, India!

SA 8000 Certification is a globally recognized standard for social accountability in the workplace. It sets the benchmark for ethical business practices, emphasizing fair treatment of workers, safe working conditions, and respect for human rights. SA 8000 helps organizations demonstrate their commitment to workers’ rights and well-being.

If you are interested in learning more about SA 8000 certification and how to get certified, please contact us today.

https://medicaldevicelicense.com/sa-8000-certification-in-baddi-india/

Social Accountability SA 8000 Certification in Baddi, India: Get certified and demonstrate your commitment to workers' rights and well-being. Contact Us Today!