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

O-Doc eBRBusiness Solutions > Software Solutions > 



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)