MEDICAL DEVICES REGISTRATION SERVICES
Permission for test license to import Medical Device (Form MD-16, Form MD-17)
In case an Importer or manufacturer of a medical device intends to import small quantities of a medical device for the purpose of training or demonstration or clinical investigations or for the purpose of testing , an application for Test License to import such products can be submitted to CDSCO under the new Medical Device Rules 2017.
The new Medical Device Rules 2017 require the manufacturer/importer to obtain a test license by applying for it using Form MD-16. Further, the test license for importing medical devices will be granted permission through Form-17.
The technical team at NKG ABC guides applicants, through this process and will helps them in obtaining the respective test license for medical device imports for the above mentioned purposes.
Application Form :
The new Medical Device Rules 2017, have categorised the notified categories of medical devices into 4 broad categories based on the risk classification of respective products. In order to PERMISSION FOR TEST LICENSE TO IMPORT MEDICAL DEVICE it is important to note the categorisation so that we can ascertain the correct fee structure applicable for the grant of approval. The below table suggests that application form , approval form, fee structure based on the risk class of products.
|
Application Form |
Approval Form |
Risk/Class A,B,C,D |
Fees |
Licensing Authority |
|
MD 16- Application for Licence to Import Medical Devices for the Purposes of Clinical Investigations or Test or Evaluation or Demonstration or Training |
MD 17- Licence to Import Medical Devices for the Purposes of Clinical Investigations or Test or Evaluation or Demonstration or Training |
A,B,C,D |
$100 |
CDSCO |
regulatory documents
A comprehensive checklist of documents has been issued by the regulatory authority which needs to be submitted for processing and grant of Import License in MD 17.
For a checklist of documents required for seeking grant of Licence to Import Medical Devices for the Purposes of Clinical Investigations or Test or Evaluation or Demonstration or Training, please click here.
Timelines
Preparing regulatory documents is a time consuming and meticulous exercise. As an importer or overseas manufacturer , one is already engrossed in various business aspects prior to placing the product in India. If a mistake is made, it can lead to complete delay in regulatory gaps, business plan, overheads, financial planning issues as well as supply chain disruption.
WHY NKG FOR Medical Device Regulatory Services
NKG has a Dedicated and Efficient team of experienced regulatory professionals who can help you Plan your regulatory needs and smoothen the process for Regulatory approvals. Strategically located in New Delhi, the “regulatory “ capital of India, NKG makes a head start by providing clear and easily understandable requirements.
in numbers from
regulatory track record
5000+
INTERNATIONAL BRANDSRegistered
100k+
Products Registered
100%
transparency & trust
proudly SUPPORTING
trade commiSsions
NKG keeps in Close communications with various Trade Commissions, Business Chambers, embassies of many countries on various existing & new Rules & Regulations of government of India
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we help you meet your compliance needs
NKG has a Dedicated and Efficient team of experienced regulatory professionals who have Registered more than 2000 brands until now who can help you Plan your regulatory needs and smoothen the process for Regulatory approvals. Strategically located in New Delhi, the “regulatory “ capital of India, NKG makes a head start by following its unique time tested “Step-by- Step “ process that puts a lot of method in between the madness.
