MedDev Experts



Medical Device Regulatory Consultancy in India - CDSCO MDR

MedDev Experts is one of the best Medical Device Regulatory Consultant in India with over 10 years’ experience. We provide consultancy services to get the Medical Device Import License and Manufacturing License from the CDSCO. 

MedDev Experts helps Medical Device manufacturers to navigate the Indian medical device 0rules. We’re experts at cutting through the paperwork and saving you money (20% off, guaranteed!). Our professional team will be with you every step of the way, getting your device approved fast so you can start selling the devices in India.

We do all the hard stuff, from documents to approvals, so you can focus on what you do best. Choose MedDev Experts and watch your medical device succeed in India!

Medical Device Regulatory Consultancy Services include:

Worried about Indian medical device regulatory compliance? Let us be your guide. We offer a tailor-made roadmap, from licenses to quality standards, to ensure your journey to success is smooth and worry-free. Contact MedDev Experts for all your Medical Device Regulatory Consultancy needs.

20% less risk, 30% faster to market! Our experts handle MD 5 & MD 9 licensing fast and compliant. Focus on innovation, we’ll handle the regulations.

Fast-track your medical device imports with our proven MD-15 Licensing expertise. Secure approvals faster, avoid delays, and get your devices to Indian market sooner. Save time and money on MD-15 applications.

Accelerate innovation with our MD-13 Medical Device Test License services. Facilitate testing, evaluation, and training of medical devices with confidence, backed by our regulatory expertise.

Ensure the market readiness of your medical devices with our certification services. From Free Sale and Market Standing Certificates to Non-Conviction and Neutral Code Certificates, we provide a comprehensive suite of certification solutions.

Expand your market presence in the U.S. with our FDA NDC Number Registration services. Whether for medical devices, over-the-counter (OTC) products, or prescription drugs, we facilitate swift and accurate registration with the U.S. FDA.

Entrust your FDA 510(k) applications to our experts for accurate and successful submissions. Benefit from our professional support to streamline the registration process and navigate FDA requirements effectively.

Embark on new ventures with confidence. Our services cover every aspect of new facility setup, from design and equipment selection to validation, compliance, and project management.

Achieve quality management excellence with our expert consultancy. Obtain certifications such as ISO 13485, ISO 9001, SA 8001, ICMED 13485 Standards, and more, ensuring compliance with international quality standards.

Navigate UDI requirements seamlessly with our services. From accurate labeling to data submission and regulatory database management, we ensure your compliance with UDI regulations.

Gain access to European markets with our CE Certification Consultancy. Our technical guidance and support pave the way for successful certification of your medical devices.

Ensure compliance with EU MDR through our comprehensive medical device labeling services. From design to implementation, we assist you in meeting the stringent requirements of European regulations.

4 Reasons Why We're Your Best Choice for Medical Device Regulatory Consultancy in India:

Expert Guidance:

Our team of seasoned professionals knows the Indian Medical Device Rules inside and out. We'll personalize a plan for your device, keeping it up-to-date with the latest standards.

Wallet-Friendly Solutions:

We get it, costs matter. That's why our services are affordable, helping you get compliant without breaking the bank.

Fast-Track to Market:

No time to waste? We've got streamlined processes and deep regulatory knowledge to get your device approved ASAP.

20% Off for You!

Because we appreciate your business, enjoy a 20% discount on our services. Top-notch compliance at a lower price? Yes, please!

Get from A to Approved with MedDev Experts:

Clear Your Hurdles:

We'll dive deep into your situation and map out your regulatory journey.

Your Custom Roadmap:

We build a personalized plan to get your device approved, fast and smooth.

Paperwork Made Easy:

Forget the red tape! We'll handle all the documents, so you can focus on your work.

Stay Compliant, Stay Happy:

We'll be your regulatory partner, keeping your device on the right track every step of the way.

Clear Your Hurdles:

We'll dive deep into your situation and map out your regulatory journey.

Fast-Track Your Medical Device Registration in India!

Don’t get bogged down by red tape. Let MedDev Experts cut through the paperwork, slash your costs (20% off!), and get your device approved ASAP.

Contact MedDev Experts today for:

  • Expert guidance: Our seasoned pros know the Indian rules like the back of their hand.
  • Fastest approvals: We’ll streamline the process to get your device to market fast.
  • Cost-effective solutions: Get compliant without breaking the bank.
  • 20% discount: Because we appreciate your business!
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