Phases of CDSCO Manufacturing license
- Phase I – Applicant Registration
- Phase II – Test License application
- Phase III – Manufacturing license application
Pre-requisite:
- Generic Name / Brand Name
- Intended Use
- Material of construction
- Mode of application
The Central Drugs Standard Control Organization (CDSCO) is the national regulatory body for Indian pharmaceuticals and medical devices, and serves parallel function to the Food and Drug Administration of the United States (FDA) it is a plan announced by the way government to bring all medical devices, including implants and contraceptives, under the view of the Central Drugs and Standard Control Organization (CDSCO).
Read More – Phases of CDSCO Manufacturing license
Medical devices consultancy 