The first eCTD submission
and management software in ASEAN


What is NVIFDA ?

NVIFDA is an eCTD submission management software with the coorporation of National Vaccine Institute (NVI) and Thai Food and Drug Administration (Thai FDA) in order to support small and medium sized pharmaceutical companies to submit required documents through electronic submission instead of traditional paper submission.

NVIFDA is an software allowing users to compile, manage, review, validate and publish regulatory documents through electronic submissions to regulatory authorities.

With close working and support from Thai FDA, the software will always comply with the latest pharmaceutical laws and regulations of new generic drugs.

Why us ?

  • Valuable price in terms of software license and maintenance fee.
  • Rapid compliance with latest regulatory changes according to Thai FDA.
  • Don’t worry for your privacy. We have an offline version.
  • Technical support team and training course are provided.

Tools

Various tools are included in both packages to ensure that
your business will continue working seamlessly.

Compile
Fill in the prepared
submission documents
into the provided panel.
Manage
Manage your documents
by easily drag and
drop into the panel.
Validate
Ensure that no invalid
submissions are
generated.
Publish
Easily publish the file
with just one click.
View
Take a look at how
the authorities see your
electronic submission.
Hyperlink
Link the related
references together.
News & Event
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Stress-regulating brain area larger in depression, bipolar
The left side of the hypothalamus was revealed to be 5 percent larger in a new study of...
10-Mar-18
Stress-regulating brain area larger in depression, bipolar
The left side of the hypothalamus was revealed to be 5 percent larger in a new study of...
10-Mar-18
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