CDSCO Manufacturing License Consultant in Gurgaon

Gurgaon, a burgeoning tech and business hub adjacent to Delhi, offers a strategic advantage for CDSCO Medical Device Manufacturing. Its modern infrastructure, coupled with a thriving corporate ecosystem, ensures seamless operations and connectivity. Gurgaon’s proximity to the capital allows easy access to regulatory bodies, while its pool of skilled professionals and technological advancements make it a conducive environment for innovation in the medical device sector. Opting for Gurgaon is a step towards combining regulatory efficiency with cutting-edge manufacturing capabilities.

Obtaining the CDSCO MD-5 and MD-9 Licenses for medical device manufacturing in India can be a complex task. But with Pharmadocx Consultants by your side, the process becomes straightforward. Pharmadocx Consultants provides consultation and regulatory services to get the license for manufacturing of Medical Devices on Form MD-5, MD-9, & Import License on MD-15.

Important Deadline for Class C and D Licensing: CDSCO has transitioned Class C and Class D rehabilitation medical devices from the mandatory registration protocol to a licensing framework as detailed in GSR 102(E) dated 11.02.2020. This pivotal transition will be operational from October 1, 2023. Official Notice – Link. This means you have till Sept 30, 2023, to apply for the License.

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Contact us today to start your journey in the world of Medical Devices!

Services Offered by Pharmadocx Consultants

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Factory Layout Design Service

We visit your premises, take measurements, and design an industry-standard layout. We provide Civil Architecture plans, Clean Room Plans of ISO Class 7, HVAC Plans, Plumbing Plans, Electrical Plans, and Equipment Plans. We design the facility as per MDR Rules 2017, USFDA 21CFR Part 820, CE guidelines. We design the facilities for efficient working with requisite cleanliness levels. Read More

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Certification Services

To register your company in overseas market, and also for scaling up your business, your manufacturing plant must be certified with regulatory bodies. We help in the entire process to make sure you never need to worry about certifications and can focus on your business. We provide certification services for GMP, GLP, WHO-GMP, COPP, ISO-13485, Free Sale Certificate from CDSCO DCGI FDA

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Regulatory Services

Pharmadocx Consultants provides regulatory work for the grant of all types of Medical Device Licenses in India - MD5, MD9, MD15, and MD42. We provide time-bound services so that our clients can start their business as fast as possible, without worrying about regulatory hurdles.

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Documentation Services

We offer support in managing and updating essential documentation needed for medical industry regulatory compliance. This encompasses QMS Documents aligned with ISO-13485 for Medical Devices, Schedule-M documents, WHO-GMP documents, and a range of Standard Operating Procedures (SOPs), Validation Documents, Plant Master Files, and Device Master Files. With a wealth of experience, our team ensures that all documents adhere to the required regulatory standards. We collaborate with our clients to keep their documentation current and precise, aiding them in achieving their quality and compliance goals.

Our Track Record Speaks for Itself!

Medical Device MD-5, MD-9 Licences

Years Experience

Plants Set-up

  • Mastery of CDSCO Guidelines: Our team is proficient in CDSCO standards and the Indian Medical Device Regulation. We align your application seamlessly with these regulations, enhancing the likelihood of prompt approval.
  • Complete Support: From the start of your registration to the moment you receive your license, we stand by you. Our thorough services guarantee that every aspect, no matter how small, is addressed.
  • Swift Application Handling: Recognizing the importance of time in the medical device sector, our efficient methods, honed over years, aim to expedite your application process.
  • Document Crafting and Verification: Leveraging our deep understanding of essential documents, from Plant Master Files to Device Master Files, we aid in their creation and meticulously check them for precision and thoroughness.

In the dynamic realm of India’s medical device regulations, the right ally can be transformative. Choose Pharmadocx Consultants as your trusted guide, steering you to triumph in India’s medical device arena. Begin your journey towards a smooth CDSCO manufacturing license with us.

Call us at 9996859227 or write to us at [email protected]

Let's Talk!

We'd love to hear from you! Whether you have questions about our pharmaceutical plant setup consultation services or want to discuss a potential project, our team is here to help. Simply fill out the form below, and we'll get back to you as soon as possible. Alternatively, you can reach out to us directly using the phone number or email address listed on this page. We look forward to connecting with you!

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  • Sonipat Office - Opposite Dewan Mill, Old D.C. Road Sonepat - 131001 Haryana, India
  • Delhi Office - G-12, Pearls Best Heights-I, Netaji Subhash Place, Delhi, 110034
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