Software Solutions

OasisLIMS

Laboratory Information Management System (LIMS) read more

LIMZ-RD

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

EnviroLIMS EWM

LIMS for environment labs, water quality monitoringread more

True-LIMZ CTL

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

Stabi-M

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

Olink

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

Business SolutionsSoftware Solutions > 


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CrisCon ERP


Key Features

CrisCon is Pharma Enterprise Resource Planning (ERP) software package to integrate all business areas in SMEs and mid-cap pharmaceutical manufacturing units Built on VB 6.0 Client/Server, MS SQL Server
CrisCon forces users to maintain entire documents/ records correctly, completely and timely, as per the regulatory requirements. It thus helps in easy implementation of cGMP, WHO GMP, Schedule M guidelines etc.
CrisCon offers a unique blend of operational knowledge, industry expertise and best practices to ensure that your goals are achieved on-time and on-budget.
CrisCon increases operational efficiencies across the enterprise and includes the activities:
  • Inventory management
  • Procurement management
  • Production Planning & Control
  • Material requirement planning (MRP)
  • Production
  • Sales
  • Warehouse management¬†
  • Financial accounting
  • Quality management
  • Human resource management, Payroll management
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Stabi-M


Key Features

Stabi-M is for scheduling of stability samples for analysis at different time intervals maintained at various experimental conditions such as temperature and humidity, for selected parameters

Other functions of this software include:

  • Stability sample pre-registration (including pack type, experimental conditions, chambers, pack size, orientation etc.)
  • Scheduling of analysis at different time intervals under various experimental conditions, for selected parameters
  • Stability testing schedule / pulls printing (date wise, product wise)
  • Stability sample login
  • Partial / reduced analysis
  • Stability work sheet
  • Stability labels
  • Analytical readings / observations / results entry
  • On-line result calculations
  • Stability COA review / approval
  • Protocol sheet generation
  • Stability graph - period wise / experimental condition wise
  • Stock report of each walk-in chamber
  • Stability sample bin card printing
  • Stability samples stock tracking including consumption records
  • Samples pending for stability login
  • Samples pending for analysis
  • Stability COA pending for review
  • Stability samples status report
  • Alerts and reminders
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CrisCon SFA


Key Features

CrisCon SFA is a Sales Force Automation System

It is a web based comprehensive software system

SFA-CRM is a solution for territory management, contact and account management for doctors, hospitals and chemists
It effectively manages field staff through tour plan, DCR and expense & gift utilization analysis
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Oasis CMS


Key Features

Oasis CMS is a Change Management System

It is a comprehensive client-server based tool

Oasis CMS is specifically designed for pharmaceutical manufacturing units, which enables the organizations to effectively manage changes to processes, documents, facilities, hardware, equipments, protocols, etc.
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O-Doc eBR


Key Features

O-Doc eBR is a software for maintenance of batch manufacturing and packaging records, electronically. It is efficient and provides safe recording, reporting, storing and retrieval of batch records
O-Doc eBR is built on VB 6.0 Client/Server
It is Microsoft Client/Sever based VBA application built for secure document management
On-line manufacturing records through electronic batch records (eBR) and electronic work instructions (EWI)
O-Doc eBR enables easy compliance with cGMP Regulations. It is standard and most appropriate tool that is specifically designed to assist in compliance with the principles of cGMP
Maintenance of BMR/BPR with electronic instructions and recording of production process data
Approvals through electronic signatures by QA at every stage of production process
It has easy interface with ERP and LIMS, and the following functional benefits:

  • Streamlined work practices / manufacturing procedures through standardization
  • Assured quality of product on-line, embedded BPR audit checks at every stage
  • Automatic tracking
  • Reduced complexity of handling paper batch records and their printing
  • Adopted rapidly by the users
  • Saves cost (reduced paper handling, reviews, and long-term storage)
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Oasis APQR


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
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Olink


Key Features

Olink is an equipment integrator

Olink GUI collects data from instruments (RS232, TCP/IP, ASCII file based) and instrument-software generated files or any ASCII file: Readily interfaces with any instrument that produces a text file

Data parsing, storing of raw data and other relevant meta data
It communicates results to LIMS in a secure central server database environment
ALso has provision to select and store chromatograms/ text/ result files which are accessible from the software for their review/report for future reference
Olink results in vast savings in time and elimination of the potential for error in transcription