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LIMS, RIMS, method validation, in-vitro releases and document management
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Founded in 1986 the iCD. GmbH is specializing in software development and related consulting of laboratories in the fields of process industries, authorities, environment, energy and water supply. iCD.-products are developed in Germany and are distributed worldwide. Additionally, subsidiary companies and partners attend to the clients at the face.
Our software solutions are applied successfully worldwide by more than 300 enterprises of different business divisions (production, quality control, R & D). Installations range from single user solutions up to applications with more than 500 users.
Products
We focus on our Laboratory Information and Management System (LIMS) LABS/Q®, the extension for syntheses and recipe optimization LABS/R which is based on LABS/Q®, the document management system DMS, the tool for method validation VALIDAT as well as our system for execution and documentation of in-vitro dissolution LABS/DS.
LABS/Q®
Laboratory information management systems (LIMS) form the backbone of almost every modern laboratory which includes electronic analysis devices. These systems are the precondition for fulfilling current requirements in the field of accredited laboratories and quality assurance. With LABS/Q® we offer a universally applicable extraordinary flexible LIMS. We can cite product installation references in nearly all industrial sectors and sizes.
By linking lab instruments and analysis systems directly to the LABS/Q® the effort of work during result entry and data transfer may be reduced dramatically. Moreover this technique will help you to eliminate potential sources of error or points of criticism during inspections. We offer to you appropriate interfaces for all known instruments and data systems.
LABS/R
For a more efficient product development we have designed a recipe information and management system (RIMS) on basis of LABS/Q® which allows the optimization of chemical syntheses and recipes.
VALIDAT
Validation of the applied analysis methods is a basic precondition for every analysis laboratory. VALIDAT will guide you safely through the planning, execution and evaluation. You will save a better part of your previous work and at the same time you will fulfil regulations of DIN, ISO, USP and ICH.
LABS/DS
In-vitro dissolution tests represent an essential aspect of quality assurance in the field of drugs. The performed tests allow conclusions on the bioavailability of the agent in the drug. In-vitro dissolution inspections are among others part of the routine inspection for pill batches in the pharmaceutical industry. Using our system LABS/DS, you will be able to automate HPLC dissolution systems in an inimitable way. The system generates authority conformable evaluations and further more offers data-recall facilities and archive features.
DMS
Our document management system is not only part of our own applications but is even implemented in other well-known software products. Its modular architecture allows the integration into existing systems, e.g. in order to fulfil requirements of the 21 CFR part 11.
Further products are XCARDS, a tool for the handling of quality control charts, LabCost®
for counting costs for laboratory processes according to the ABC-method and LabCos®
, a software for recipe management, recipe optimization and quality control.
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