Accelerate Your Biopharma R&D with IDBS Polar, the World's Best Scientific Process Management Platform

Today, the development of new biologics takes almost 10 to 13 years with a cost of more than 1 billion USD to bring to market. To shorten this massive journey, biopharma development teams can leverage the power of connected technology that interfaces with a wide-range of R&D instruments, LIMS, and other electronic devices to achieve faster method development and conduct of experiments. The need of the hour is to harmonize data collection, information sharing, and gaining actionable insights across biopharma processes such as cell-line development, upstream and downstream processing, and bioanalytical development.

To address this industry challenge, Techsol has partnered with IDBS which specializes in providing purpose-built software solutions to address the data management challenges prominent across the BioPharma lifecycle and supply chain. IDBS Polar and Skyland PIMS platforms enable customers in research, development and manufacturing to efficiently and compliantly access crticial data and insights to make faster, smarter decisions with greater confidence.

Introducing IDBS Polar

IDBS Polar, a cloud-based BioPharma Lifecycle Management (BPLM) platform, helps to efficiently execute your processes while curating the data you need to accelerate time to market by tackling the biggest challenges in process design, optimization, scale-up and technology transfer. There are two main applications which are part of the core IDBS Polar platform. 

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IDBS Polar BioAnalysis enables CROs and biopharma to improve quality and reproducibility, reduce study cycle times and accelerate time-to-market. With 25 years experience, IDBS best practice workflows to optimize quality, data accuracy and operational efficiency for developing methods and conducting experiments.

Facilitates Integrated inventory management along with tracking the entire sample lifecycle which results in 50% lesser documentation time.

Enable Study Directors and Principal Investigators to define the recipes, procedures and parameters of the methods and assays that will be conducted, ensuring that execution is repeatable.

Document the procedures and preparations of bioanalysis, ensuring quality while retaining flexibility. Capture data in a consistent and traceable way, flag exceptions in process for immediate correction or explanation, and log all items used including genealogy tracking

Summarize results across the execution workflows within a study including the calibration curve, quality controls, validation and stability assessment sample.

Early Phase Clinical Trials | Techsol Life Sciences
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