Sensyo Life Sciences provides global regulatory, compliance, and validation consulting services to the pharmaceutical, biologics, veterinary and medical device industries. Sensyo has assisted many pharmaceutical, medical device and biologics companies successfully meet regulatory requirements as well as their target business objectives.
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Sensyo's compliance and regulatory affairs staff comes from a wide range of therapeutic backgrounds. Experienced in the development of submission strategies that expedite agency review, we provide comprehensive compliance and regulatory services and expertise in the areas of chemistry manufacturing and control (CMC), chemistry and pharmacy development, and international regulatory strategies.

Sensyo Technologies provides a complete solution suite based on operations business process management. SmartAdvance™ Solutions are based on the Integral-Nodes methodology and information technology.

SmartAdvance™ Solutions model, control and track all aspects of production on the plant floor, while providing a detailed and complete history for compliance and performance improvements.

Sensyo's SmartAdvance™ solution reduces the complexity of integrating multiple systems and achieves a significant reduction in cost in terms of ownership, maintenance and programming time.

Manufacturing execution systems: moving to the next level
The use of manufacturing execution systems (MESs) can provide important information to all parts of the pharma manufacturing business...

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How MES provide a new perspective on quality control
How MES (Manufacturing Execution Systems) provide a new perspective on quality control. (Editor's Spotlight)...

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