Software Solutions


Laboratory Information Management System (LIMS) read more


For R&D centers / labs, for automation of R&D activities in pharma research specially in FD division and ADLread more


LIMS for environment labs, water quality monitoringread more


LIMS for commercial testing labs (with integrated billing)read more


True web based enterprise software for stability studies data management and compliance with US FDA 21 CFR Part 11read more


Equipment connectivity, to efficiently transfer analytical data from instruments to OasisLIMS read more

CrisCon ERP

Pharma ERP - Enterprise version: Specially designed to automate various activities of manufacturing unitsread more

CrisCon SFA

Sales force automation, web basedread more

Oasis CMS

Change management and control systemread more

O-Doc eBR

Electronic batch records maintenance software with electronic instructionsread more

Oasis APQR

Annual product quality review and records of batches producedread more

Oasis APQRBusiness Solutions > Software Solutions > 

Key Features

Oasis APQR is a solution for annual product quality review for all the batches of a finished product manufactured during the year / period
It is web based built on ASP.Net with the option of MS SQL Server/Oracle Database, central server deployment, scale-able up to 150 users. The benefits and functions of Oasis APQR are highlighted below:

  • Decreases the risk of out-of-specification results
  • Minimizes the risk of rework/reprocessing
  • Decreases downtime
  • Increases productivity
  • Decreases the risk of product recalls
  • Meets all regulatory commitments/requirements
  • Improves communication between production, engineering, quality and regulatory functions
  • Recording of process / raw data on various stages; graphical representation of processing parameters
  • Generation of trend on yield
  • Generation of reports from LIMS on various quality attributes of finished product
  • Storage, maintenance and generation of exhaustive reports on stability studies at different experimental conditions, time points and packaging conditions
  • Data trending of selected tests and graphical representation of analytical data
  • Provision to record and maintain summary and discussion of quality attributes
  • Provision to maintain market complaints data, product recall data
  • Deviations and OOS results handling
  • Change control and failures