Instem and PharmQuest now provide one synergistic cutting edge system, which is supported by professional Instem Solution Services that meet your needs and is governed by a rigorous methodology to ensure successful outcomes - on time and to budget.
The power of partnership working for you
Join us in supporting this important initiative and by becoming SENDReady now, you will have peace of mind knowing that your costs will be contained, that you will be SEND-enabled and ready to submit within 90-days of the FDA's final guidance. Through submit, will take the additional step and ensure that any changes in the submission standards before or after guidance are included.
Benefit by being Proactive
The FDA is urging industry to begin
planning how they will respond to the new SEND standards
and is ready to issue final guidance. They see this
initiative as part of the vital program in helping
to bring new discoveries to the public more quickly,
efficiently and safely.
Join other leading organizations by speaking with
us today. We offer cutting edge technology solutions
that were developed with industry and the FDA - for
you to realize operational efficiencies while supporting
the FDA in its quest to overcome the challenges of
managing vast amounts of critical information.
Options to Fit Your Needs
Submission-Based
Pricing
Subscription-Based

SENDReady
Analysis - Understanding Your Options…
Our SENDReady Analysis is a professional consultative
visit that assesses your environment, all of your source
systems and delivers a functional, value-added and objective
report. It clearly recommends in detail your options
for becoming SEND-enabled with or without deploying
a submit solution, and why.
To discuss your SENDReady Analysis
please contact us at:
Tel: +1 (650) 350-1900 or e-mail: 
Tel: (610) 941-0990 or e-mail: submit@instem-LSS.com