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

OasisLIMSLims > Software Solutions > 

OasisLIMS is the most comprehensive LIMS software which helps you comply with Schedule L-1 of Drugs and Cosmetics Rules (GLP), US FDA 21 CFR Part 11 norms, PIC/S and EU Annexure 11 guidelines. Our LIMS range includes:
  • OasisLIMS
  • OasisLIMS EL
  • OasisLIMS Web based


  • Covers about 70% of the activities / requirements laid down in GLP; remaining about 30% requirements are relating to premises, infrastructure, manual working etc.
  • Through OasisLIMS the documentation is better organized and maintained, always up-to-date for auditing and inspections
  • It is regularly updated with amendments in pharmacopoeias / D&C Act and the Rules/ in-house
  • It is customizable, flexible and functionally rich, ready to accommodate any type of requirement, as per your needs

OasisLIMS saves

  • Cost in QA, QC operations
  • Valuable man-hours of technical staff
  • Time spent on calculations
  • Time spent in writing and checking reports
  • The time saved is utilized for other important and productive tasks in the lab

Key features

Test Methods/Calculations
  • Automatic on-line calculations for more than 175 test methods as per IP / BP / USP / in-house including titrations, dissolution, weight variation, content uniformity, UV, GC/ HPLC etc.
  • Eliminates possibilities of calculation mistakes
  • No time is consumed in calculations: saves significant time of chemists
  • Pre-defined values for dilutions, titration factors, wavelengths, other constants
  • No need to define external formula for calculations
  • One test method can be used for ā€˜nā€™ no. of products
  • No need to maintain notebooks for calculations
  • Validated test methods, no-need to verify/ check results
  • Validity checks at all possible levels
Specification Maintenance
  • Specifications for raw materials / packing materials / intermediates / bulk / finished products easily maintained, with the facility of revisions history
  • No need to refer to specifications repeatedly at the time of analysis
  • Facility to maintain SOPs, STPs, calibration procedures, with revision history
Sample login / Registration
  • On GRN / production intimation, sample login takes place in the software with minimum parameters
  • Allows many types of logins such as normal sample, retest, pre-shipment / pre-purchase, OOS, R&D etc.
  • Automatic, unique AR No. (analytical report number) generation for different categories of samples
  • Facility to enter sampling plan for every product/material
  • Sampling details and sampling observation entry
  • Option of partial/reduced analysis
  • Tests automatically allocated to the sample 
Work sheets / protocol sheets
  • Automatic generation of worksheets dynamically, for raw materials / packing materials / intermediates / bulk / finished products, indicating all the tests to be performed as per pharmacopoeia (IP / BP/ USP etc. and/or in-house specifications).
  • User defined formats for entry of readings / observations, as per drugs and cosmetic act and the rules
  • Work sheet may also incorporate method of analysis
  • Calculation sheet (raw data sheet) automatically generated
Generation of COA - Certificate of Analysis
  • Printing as per pharmacopoeial, regulatory requirements
  • Integrity pre-established; no need to check individual report
  • Automatic cross verification of results with the specification limits
  • Automatic decision of approval/conformance or rejection/non-conformance of sample
  • Opinion includes rejection parameters/test also
  • System itself is designed to take decision independently
  • Eliminates possibility of biased opinion
  • Saves lot of time of senior chemists, senior chemists can focus on value added tasks
MIS and other reports
  • Work sheet, CoA, Specifications, SOPs, STPs
  • Sampling sheet, Sample register (category wise), Rejection register
  • Labels (under test, approved, rejected, sampled, quarantined etc.)
  • QC productivity report
  • Analyst performance report
  • Samples pending for sampling
  • Samples pending for analysis
  • Samples pending for entry of readings / observations
  • COA pending for review
  • COA pending for printing
  • Lab performance report on various parameters
  • Sample approval status
  • Samples for retest
  • Products (control samples) for destruction