lims software providers

LIMS manages the data flow from within an organization and centralizes the data into one central database. LIMS solutions, especially those integrated with Scientific Data Management Systems (SDMS), should unify large volumes of biological and chemical information into a single browser-based interface. This data can then be made available electronically to people and systems that require it. LIMS thus becomes a comprehensive solution that enables pharmaceutical research organizations to focus time and effort on production of scientific information, valuable in developing new drug formulations ahead of the competition. Lims Software Lab Management Software Data Integrity Sdms Software Eln Software

Clinical Research Clinical Research is crucial in the study of drugs that are supposed to reach the market right from pre-clinical through all the phases I- IV. Being subject to regulatory compliance it is indispensable for them to have flawless processes and data with high level of integrity in place. QuaLIS Clinical Trial Management App collection helps the industry right from pre-clinical through all the phases of clinical trial management. The solution includes a clinical LIS for volunteer screening and testing. InterFACER the clinical instrument interface middleware is deployed for interfacing clinical instruments. A volunteer database management system including biometric identification and screening handles the volunteers for clinical studies. A study protocol configuration module helps in creating studies. A dynamic user modifiable CRF module helps in creating various templates for study recording. Phlebotomy, dietary, vitals recording, sample processing and storag...

LogiLAB® ELN is an Electronic Lab Notebook Software enables electronic form-based data capture for laboratories. Traditionally used in discovery research, ELN Software today is important for quality control and R&D labs across industries. They aid regulated industries to move towards a paperless digital era, improve compliance with regulatory norms, GLP, 21 CFR Part 11 and EudraLex Annex 11 to name a few.

Document management software is an online document management software solution  that helps to  automate entire organization’s documents with complete control and traceability.  Th e software  helps an organization in  organizing, mana ging, sharing and communicating internal business information. It is known for being time saving and energy efficient.   Qua LIS document management software from Agaram Technologies ensures that  the sophisticated system eliminates every risk of out of date documentation. It  works towards making everything run on time with no setbacks.  Moreover, QuaLIS DMS regulates industries and  helps them stay compliant  with  21 cfr part 11 compliance   and  E udraLex Annex 11 compliance. It also ensures that it stays within the  latest data integrity guidelines . With such compliance, comes peace of mind from audits by regulators or customers.   The software has been d...

QuaLIS® LIMS was originally designed for the pharmaceutical industry, unlike any other generic LIMS. QuaLIS is a powerful enterprise-scale LIMS developed using a strong framework and is fully configurable and customizable for regulated pharmaceutical QA/QC, R&D and analytical development environment. QuaLIS LIMS covers all the workflow processes within a typical regulated laboratory. It addresses several pain points of the industry and saves >50% of the time and human effort with respect to data capture, review and approvals. QuaLIS is quite different from the regular LIMS which are generic in nature and require considerable consulting and professional services to meet industry needs. Having been built from scratch, for the pharmaceutical industry, it addresses GLP and 21 CFR Part 11 Compliance / EudraLex Annex 11 guidelines. Today, very few LIMS in the international market can match the capabilities of this system. For more info visit Lims software provider in ind...

Data integrity is the  accuracy and validity of data that exists even after its life.  For enterpris es that depend on these data, they are mainly expected to be precise and reliable.  Then, there’s always the  risk of losing sensitive data or data manipulation.  This is the main reason that  data integrity solutions play a major role in the security of enterprises.   When talking about security, data integrity can be compromised in many ways.  Transfer of data  might result in  altered or removed information.  This is where  data integrity software comes into play to monitor data integrity issues.   The soft ware needs to support 21 CFR Part 11 compliance . This ensures compatibility with multiple platforms  of different servers and browsers.   Maintaining proper data integrity is important for any organization, especially in the pharma biotech sector. Making sure that the data produced is accura...

InterFACER is a middleware to interface clinical in-vitro diagnostic instrument & point-of-care diagnostic space. The basic concept design of InterFACER was in itself solution-oriented *  reducing vendor dependency & increasing flexibility to switch instruments assisting the diagnostics world. Integrate clinical analysers of haematology, biochemistry, blood gas, immune assay, ELISA, microbiology, molecular diagnostic discipline or any LIS or LIMS / healthcare system with ease. InterFACER middleware helps clinical diagnostic pathology laboratories, clinical research, public health labs, blood banks, biobanks in improving throughput.