PRICING
Explore our transparent pricing structure for regulatory certification services, including CE-Medical, CE-IVD, UKCA, CDSCO and US FDA 510(k). Each section provides detailed cost estimates for documentation development, coordination, and approved body assessment.
CDSCO License Services Pricing
At Pharmadocx Consultants, we specialize in providing complete regulatory support for obtaining CDSCO Medical Device Licenses in India. Our expert team assists with MD-5 and MD-9 Manufacturing Licenses, as well as MD-15 and MD-17 Import Licenses under the Medical Device Rules (MDR) 2017. Whether you are a domestic manufacturer or an international importer, we ensure smooth coordination, documentation, and regulatory compliance with CDSCO requirements.
Pricing for CDSCO license services varies based on the device class, type, and scope of application. To receive a customized quotation tailored to your specific medical device, please contact us directly via phone, email, or WhatsApp.
CE Medical Device Certification (EU MDR)
Pricing Structure in EUR — Transparent cost estimates for documentation development, coordination, and notified body assessment. Final costs depend on device specifics.
| Service Category | Class I | Is / Im / Ir | IIa / IIa (Active) | IIb / IIb (Active) | Class III |
|---|---|---|---|---|---|
| Technical Documentation & Notified Body Coordination Through Certification | 3,500 | 5,000 | 7,000 / 8,000 | 9,000 / 12,000 | 14,000 |
| Notified Body Assessment Fees (Estimated) | N/A | 12,000–15,000 | 15,000–20,000 | 20,000–25,000 | 25,000–30,000 |
| EAR Fee | 1,200 | 1,200–1,400 | 1,400–1,800 | 1,800–2,000 | 2,000–2,500 |
Important Information
- Pricing is indicative per single-product submission and varies by intended use and classification codes.
- Final costs depend on product complexity, variants, lab testing, and notified/approved body fees.