Guidance & Resources
Thai FDA ยท MDCD ยท CSDT templates ยท Positive List ยท e-Submission
Key Thai FDA / MDCD Documentsโ
| Document | Content | Where to Find |
|---|---|---|
| CSDT Full format template | Mandatory dossier format for Class 2โ4 | Thai FDA website |
| Class 1 Listing form | Application form for Positive List devices | Thai FDA website |
| Positive List โ Class 1 devices | Current list of devices eligible for Listing pathway | Thai FDA website (updated periodically) |
| Grouping guidance | Eligibility rules for Family/System/Set/IVD grouping | Thai FDA website |
| Classification reference list | MoPH classification notification and examples | Thai FDA website |
| e-Submission portal guide | How to register and use the Thai FDA online portal | Thai FDA website |
| Fee schedule | Registration, Establishment License, and renewal fees | Thai FDA website |
Processing Timelines by Pathwayโ
| Pathway | Standard Route | Concise/Reliance Route |
|---|---|---|
| Class 1 Listing | Daysโweeks (automatic) | N/A |
| Class 2โ3 Notification | 2โ4 months | 1โ3 months |
| Class 4 License | 4โ8+ months | 3โ5 months |
Note: Timelines are approximate and subject to Thai FDA workload, dossier completeness, and device complexity.
ISO Standards Quick Referenceโ
| Standard | Required For |
|---|---|
| ISO 13485:2016 | All Class 2/3/4 โ manufacturer QMS |
| ISO 14971:2019 | All registered devices โ risk management |
| IEC 62304 | SaMD โ software lifecycle |
| IEC 62366-1 | Usability engineering |
| ISO 10993 series | Biocompatibility |
| IEC 60601-1 | Active/electrical devices |
| IEC 60601-1-2 | EMC |
Official Sourceโ
All forms, templates, Positive List, and guidance: Thai FDA website โ www.fda.moph.go.th โ Medical Devices section โ MDCD
Download fresh versions
The Positive List is updated when new Class 1 devices are added. Always download the current version before assuming a device is eligible for Listing.