Logiciel LIMS Recherche et développement

The Main Challenges of Digitalizing Your Laboratory

The R&D LIMS solution boosts productivity by automating time-consuming tasks, allowing researchers to focus on conducting experiments and analyzing results.

It also enhances the utilization of the laboratory’s technical assets by simplifying traceability and technical data analysis. Additionally, it supports compliance with regulatory requirements and improves customer satisfaction by streamlining the management of complaints and non-conformities.

TEEXMA for LIMS R&D Solution: A LIMS Software Tailored for R&D Laboratories

Strengthen your laboratory's information system with the TEEXMA for LIMS R&D solution, available in SaaS, Cloud, or On-Premise deployment options.

Designed for R&D testing laboratories, our LIMS solution ensures digital continuity throughout the lifecycle of requests and experiments.

Industry 4.0 is waiting for you—enhance digital continuity by digitalizing your R&D laboratory activities.

Benefits of TEEXMA for LIMS
R&D Solution

Increase productivity and meet deadlines

Thanks to the digital continuity supported by TEEXMA for LIMS, your technicians can concentrate on their core business: carrying out tests and analyzing results in response to customer requests.

Facilitate the organization's regulatory compliance

Deploying TEEXMA for LIMS within your organization is a gas pedal for certifications (ISO 17025, 21 CFR PART 11, BLP, etc.): traceability and transactions (Audit Trail), validation processes and electronic signature, etc.

Increase productivity and meet deadlines

With the digital continuity provided by TEEXMA for LIMS, your technicians can focus on their core tasks: conducting experiments and analyzing results to meet client requests.

Simplify regulatory compliance

Deploying TEEXMA for LIMS within your organization accelerates certifications (ISO 17025, 21 CFR PART 11, GLP, etc.) by offering features like traceability and transaction tracking (Audit Trail), validation processes, and electronic signatures.

Enhance laboratory quality

TEEXMA for LIMS includes management tools for quality documents (procedures, technical instructions, operating methods) and customer complaints, from reporting to handling non-conformities (discrepancy reports and corrective actions).

Leverage and capitalize on technical assets

Built-in text and multi-criteria search functions in TEEXMA for LIMS make it easy to compare data and conduct statistical analyses within your technical assets.

Benefits of TEEXMA for LIMS
R&D solution

Increase productivity and meet deadlines

With the digital continuity provided by TEEXMA for LIMS, your technicians can focus on their core tasks: conducting experiments and analyzing results to meet client requests.

Simplify regulatory compliance

Deploying TEEXMA for LIMS within your organization accelerates certifications (ISO 17025, 21 CFR PART 11, GLP, etc.) by offering features like traceability and transaction tracking (Audit Trail), validation processes, and electronic signatures.

Enhance laboratory quality

TEEXMA for LIMS includes management tools for quality documents (procedures, technical instructions, operating methods) and customer complaints, from reporting to handling non-conformities (discrepancy reports and corrective actions).

Leverage and capitalize on technical assets

Built-in text and multi-criteria search functions in TEEXMA for LIMS make it easy to compare data and conduct statistical analyses within your technical assets.

Key features of TEEXMA for LIMS
R&D solution

Our LIMS software ensures digital continuity throughout the entire requisition and test lifecycle. From request creation to sample management, test activity planning and results consolidation, LIMS software centralizes, tracks and secures all data and knowledge produced by the laboratory at every stage of the process. The modules making up our R&D LIMS offer can be fully customized to meet specific needs, improve laboratory productivity and facilitate compliance with current regulations (ISO 17025, GLP, 21 CFR Part 11...).

Test request management

Gestion des demandes d'essais
Planification de l'activité du laboratoire

Laboratory activity planning

Product tracking

Suivi des produits

Capitalizing on results

Report generation

Operating technical assets