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.




Enquire Now



GET CERTIFIED IN 5 STEPS


Send an Enquiry to us.

Get a 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 necessary regulatory guidelines, appropriate for policy authority for the regulatory proposal.

Get Audited by Regulatory agency/ 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 regulatory body!

OUR EXPERTISE

Transparency

approach for overall regulatory consultation process.

Documentation

Rely on us for well documentation process.

Support

– Avail our support team post consultation as well.


Strategy

offers a comprehensive elucidation of the project.



56

GLOBAL LOCATION



178

CONSULTANTS



3789

CERTIFICATIONS



100%

HAPPY CLIENTS



FEEDBACKS

People Say Nicest Thing

NEWS

From Our Blog

How do we help your Business
How do we Help your Business?
  • Feb 26, 2018
  • By Admin
  • Comment (20)
  • Like (53)