Why We’re Preferred2018-08-14T13:37:43+00:00

Why We’re Preferred

We are passionate about developing and launching combination products.

Medical Device and Biopharmaceutical companies gain an edge by utilizing ZebraSci. Our technologies, combination product development services and ISO 17025:2005 accredited  testing lab provide the resources you need for your medical device and combination product development project.

Our experienced team has provided solutions for drug delivery devices and combination products for nearly ten years. Our cross-functional team is geared to deliver thoughtful, integrated solutions to your device projects. We’re not your ordinary CRO – we’ve got you covered from Concept to Commercialization.

Why We’re Preferred

Track Record

ZebraSci works with 100’s of medical device manufacturers

Proven Results

By combining experience, a unique methodology, customized tools and a passion for results, we help our clients produce tangible results from strategy through launch.

Why We’re Preferred

Testing

Our in-house, independent test lab has all the solutions you need

Advanced Capabilities

Our ISO 17025 accredited testing laboratory for primary container engineering, medical device, drug delivery & combination product development provides the testing solutions you need.

Why We’re Preferred

Technology

Our advanced automated inspection machines are state of the art

Our Innovative Tech

Our inspection products help you characterize silicone oil coverage, particulates, fill volume, dimensional characteristics and visual defects of primary containers.

Our Approach

We partner with our clients from concept to commercialization for combination product development.  ZebraSci’s experienced team can help you select primary containers, establish device performance specifications, develop design verification testing plans and execute all the required testing. Our complaint handling and root cause analysis programs help you manage your device post-launch. Our consultation and highly-developed validation and qualification procedures, ensure that your device comes to market on time, on budget and in compliance with ISO 13485 and FDA 21 CFR 820.