In recent years, the life sciences/pharma industries are forced to try and reinvent themselves in the challenging business environment. The pharmaceutical industry is at crossroads. They are being forced to have IT as a facilitator to create global collaborative work environment and mandatory regulatory compliances to overcome the impact of law. IT process has to be robust enough to capture all these details and streamline their business procedures.
Indium focuses on some of the typical Life Sciences/Pharma applications such as Process Control Systems, Laboratory Information Management Systems (LIMS), Clinical Trials, Clinical Data Warehousing Solutions, Electronic Data Capture System, Advanced Laboratory Testing, and Research Content Management Software. Our testing COE has a dedicated team of QA specialists with decades of combined experience in this space.
With extensive experience helping top organizations implement a broad range of software validation and verification based on GAMP and cGMPs, Indium’s consultants use best practices in testing of IQ/OQ/PQ protocols and provide documentation on test scripts/results.
Indium experts’ also helps regulated industries to comply with FDA regulations 21 CFR Part 11, Part 820 and Part 58 mandate to provide system assurance.
In addition to our broad range of services, Indium also provides jump start kits (Domain Expertise, Validation and Document templates) that address immediate requirements.