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A SPECIAL
ANNOUNCEMENT FROM: |
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We are so sure you will want to read the guidance overview that we are offering free coffee for the first 50 participants to enjoy. |
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Regulatory
pressures have been increasing over the past year. FDA and EU GDP
audits are keeping API manufacturers up at night. Are you prepared for
when they knock on your door? As an API manufacturer, you will be
accountable for proper storage, handling, and distribution of your
products across a complex supply chain. Most importantly, there is a
requirement for documenting appropriate temperature according to the
published label claim.
Let Sensitech help.
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First,
we have prepared a comprehensive overview of the latest global
regulatory and standard-based guidance that will help you to ensure
compliance with the broader market expectations.
Second,
we have been working with pharmaceutical manufacturers for over 25
years helping them to document regulatory compliance while working to
lower costs and mitigate risks associated with the storage, handling,
and distribution of time and temperature sensitive products. We even
offer easy-to-implement solutions that collect and disseminate both
environmental conditions and location of high-value shipments in
real-time – allowing you to remain informed of the condition and
location of your product virtually anytime, anyplace in the world.
FREE COFFEE TO THE FIRST 50 PARTICIPANTS! CLICK THE LINK AND REGISTER.
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