Regularity Affair

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We always believe that Regulatory affairs are “Backbone of Pharma Industry”. Our in-house regulatory team has achieved great outcomes by constantly working and acting as an interface between our customers and their respective regulatory agencies and regulatory affairs departments spread across the Globe to achieve smooth transmission of information and compliances.

Tashi Pharma provides complete support from product registrations to final regulatory agencies and tries to accomplish all activities to obtain product approvals/marketing authorization.

Our team has in depth and extensive knowledge of regulatory requirements in almost all markets across the globe. This helps us to achieve great results against ever-changing challenging market and regulatory requirements. Also our team has level best experience of submissions associated with almost all therapeutic categories which ensures our customers that they are at right place and can access our expertise at each stage of regulatory requirements.

Our regulatory affairs services help

our customers achieve the following:

Drug Master files

New drug application

Design and Packaging


Mitigate the time taken for a product to reach the market

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