Sensitech

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A SPECIAL
ANNOUNCEMENT FROM:

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.

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.

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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