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IVD Regulatory Consultants in India - In Vitro Diagnostics (IVD) Regulatory Services, IVD Device Registration and Approval, IVD Registration and Approval Consulting. For IVD Regulatory Affairs call +91 7672005050

Import License For IVD, In-Vitro Diagnostic Kits License for importers, Form MD14, MD15. Get Permission to Import Predicate In-Vitro Diagnostic Kits (Form MD14, MD15). Call 7672005050.

Procedure to Get manufacturing/import license for new Medical Devices India, Call @ +91 7672005050 to get the permission to import or manufacture new medical device.

It's time to accelerate your reach of cosmetic products to the Indian market. As per the New Cosmetic rule 2020, Cosmetic product registration certificate (COS-2) can now be obtained by filing an application in Form COS 1. 

Cosmetic registration, cosmetic product registration for obtaining a cosmetic registration certificate, and dealing with cosmetic compliance and claims could be overwhelming experiences for many. 

A regulatory expert like CliniExperts can help you throughout this journey and even with cosmetic label compliance and claims if you're planning to venture into the Indian market.

We bring clarity on topics like what are Form COS 1 & Form COS 2 and many more, like how to apply for - Cosmetic Registration Certificate (COS- 2) in India? Here's the answer to just that: 

Registration of importer on SUGAM 

Document compilation for application filing 

Upload essential documents online 

Pay government fee and upload the challan 

Generate COS-1 and upload signed Form COS-1

Medical device regulatory consultants in India, medical device registration & approval services by CliniExperts. For medical device regulatory services; call +91 7672005050

CliniExperts Services provides medical device consulting services for medical device manufacturers and importers. With 13 years of experience, CliniExperts as Medical Device Authorize Agent/ Medical Device Regulatory Consultants strives to offer Technical and Regulatory Support to both Indian Medical Device Manufacturers.

Objectives of CliniExperts Medical Devices Consultancy Services

Seamless Regulatory Approval Process for Indian Manufacturers, Foreign Manufacturers, and Importers of Medical Devices

Why Choose CliniExperts as Medical Device Regulatory Consultants In India

An exceptional Indian company with expertise in regulatory services for the pharma industry is now extending its outstanding services to the field of medical devices. With over a decade of experience, we take pride in our highly satisfied global client base.

Our comprehensive portfolio of end-to-end medical devices regulatory services includes the following steps to ensure proper regulation for your proposed medical device product: 

a. Pre-Registration Consulting 

b. Preparation of the necessary Documentation Kit for accurate submission 

c. In-process facilitation services 

d. Final Regulatory presentation and approvals 

e. post-Approval consulting services 

f. Client Feedback