POST APPROVAL CHANGES for ivd
Get authorized agent support for all your post approval changes to In-Vitro Diagnostic Kits substance for already approved IVD manufacturing site

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POST APPROVAL CHANGES for medical devices
Get authorized agent support for all your post approval changes to Medical Device substance for already approved Medical Device manufacturing site

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Model Approval in India
At CliniExperts, we ensure that your approval does not extend while you work on launching your product in the market.

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Permission to Manufacture Class C & D In- Vitro Diagnostics
Cliniexperts provides you with a one-stop solution for your IVD products needs right from test or Manufacture licenses to manufacturing and post-marketing licenses.

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Permission to Manufacture Class C & D Medical Devices
CliniExperts can functions as authorized agent in India. It has a firm position in the Indian Healthcare market, and holds a valid Drug Wholesale License.

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POST APPROVAL CHANGES For Drugs
Get authorized agent support for all your post approval changes to drug substance for already approved drugs or drug manufacturing site.

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POST APPROVAL CHANGES For Biologicals
Get authorized agent support for all your post approval changes to biological substance for already approved biologicals manufacturing site

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Test license to manufacture In Vitro Diagnostics in India – MD 12 & MD 13
Registration for in-vitro diagnostic medical devices for manufacturing can be time-consuming and tedious

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Permission to Manufacture Class A-B Medical Devices in India – Form MD 3 & MD 5
The application for manufacturing, sale or distribution of any medical device includes a tedious list of processes and forms

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COSMETIC LABEL COMPLIANCE
CliniExperts regulatory advisers help to evaluate all aspects from legal to regulatory compliances for Cosmetic to meet all the requirements in the form directives, regulations and standards stated by CDSCO.

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