Regulatory Consultations

Achieve this Regulatory Consultations in a hassle free approach. Simpler, Faster and Affordable.

LITTLE ABOUT

Why you Need Regulatory Consultations

Regulatory consultations are advantageous and promoting for new as well as existing pharma companies. Our expertise operates and perform quality chore on Drug Master File (USDMF) type II and III filings , Active Substance Master File (ASMF). Marketing authorization submissions to USA -ANDA (Abbreviated New drug Application) and to agencies of Europe, Canada and ROW countries.

Aim to offer quality compliance with speed reviews and regulatory consultations to meet the highly sophisticated competitive industry.




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GET CERTIFIED IN 5 STEPS


Send an Enquiry to us.

Get a FREE GAP analysis of your company done and receive a quote.

Accept quote and initiate the process

Once the quote is accepted we will initiate the implementation process as per the guidelines.

Get trained and Implement the guidelines

We will provide the required trainings and documentation support to fulfill the Regulatory Consultations.

Get Audited by Certification body!

Take the final external audit in our presence and accomplish it successfully.

Receive Certificate and Make Payment !

Receive the final hard copy of the certificate from the certification body !

OUR EXPERTISE

Training

Provided by expert consultants from across all industry domains.

Documentation

We follow a well documented approach for your certification process.

Support

Avail access to our 24X7 support team post certification as well.


Guaranteed

With TopCertifier it is Certification Guaranteed. No Certification, No Fees !



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