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Liveo EZ Switch®

Major challenge in post approval change in the Pharmaceutical packaging is belief the benefit of the change does not justify the cost of the resources required to make the change. This often creates a psychological barrier in the pharmaceutical industry for creating commercially and scientifically beneficial changes.

Liveo’s EZ Switch® Program is the ideal solution to overcome this challenge and to make the change as an easy and seamless process.

EZ Switch® is registrated trademark of Liveo Research Inc.
EZ Switch®
EZ Switch®

Scientific Packaging Service

This program is designed to take away customer’s pain and risk. The process is designed and executed by adapting the principle laid out in FDA’s guideline to the industry on “post approval changes for NDA and ANDA drugs”. Liveo Research’s unmatched pharma packaging testing tools and resources support customers in every stage of the process.
  • Packaging cost evaluation to visualize potential packaging cost saving with different packaging options
  • Equivalency study report in lieu of stability study data to prove “equal or better” as per interchange-ability protocol justifying for minor change.
  • Satisfies the regulatory and quality requirements with full documentation essential for  change control management
  • Onsite supports for machine validation and optimizing the machine parameters.

 It’s that "EZ"!

The Liveo +

Quality and Regulatory

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