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Text Content

 * Solutions
 * Use Cases
 * About lexoro
 * Services
 * Career
 * Contact

 * English


 * Solutions
   
   INDUSTRY
   
    * MedTech
    * Pharmaceutical
    * Chemistry
   
   COMPETENCE
   
    * Regulatory Affairs
    * Clinical Affairs
    * Quality Management
    * Risk Management
    * Medical Affairs
    * Post-Market Surveillance
    * Product Safety
   
   TECHNOLOGY
   
    * Robotic Process Automation
    * Natural Language Processing
    * Natural Language Generation

 * Use Cases
 * About lexoro
    * About lexoro
    * Insights
    * Tech Stack

 * Services
 * Career
 * Contact

 * English

INDUSTRY

 * MedTech
 * Pharmaceutical
 * Chemistry

COMPETENCE

 * Regulatory Affairs
 * Clinical Affairs
 * Quality Management
 * Risk Management
 * Medical Affairs
 * Post-Market Surveillance
 * Product Safety

TECHNOLOGY

 * Robotic Process Automation
 * Natural Language Processing
 * Natural Language Generation

COMPETENCEFOCUSTECHFOCUSINDUSTRYFOCUS
 * About lexoro
 * Insights
 * Tech Stack



The pulse of A.I.


AUTOMATED GENERATION OF
25.000 PAGES MEDICAL WRITING

Using RPA, NLP and NLG technologies we automated the generation of clinical
study reports (CSR). For our client from Pharmaceutical industry we automated
the data transfer from Clinical Study Protocol to Clinical Study Report.
Read Use Case→


The Pulse of A.I.


INTELLIGENT AUTOMATION IN HIGHLY REGULATED INDUSTRIES

We automate regulatory tasks and workflows along all areas of the product life
cycle. Our focus: MedTech, Pharmaceutical and Chemical industries.
Who we are→
Watch video

The pulse of A.I.


WE AUTOMATE CLINICAL
STUDY REPORTS WITH RPA

100% error-free: Using RPA technology, we have automated the transfer of
information from Clinical Study Reports, internal systems and the filling of
documents and templates to 100% error-free.
More about RPA→


The pulse of A.I.


70 PERCENT
AUTOMATED PQRS USING RPA AND NLP TECHNOLOGY

Saving time and top experts can focus on other topics: Using 100% error-free RPA
and NLP technology, lexoro has automated the data transfer processes and the
creation of product quality reviews in Pharmaceutical industry.
Read Use Case→


The pulse of A.I.


AUTOMATED GENERATION OF
25.000 PAGES MEDICAL WRITING

Using RPA, NLP and NLG technologies we automated the generation of clinical
study reports (CSR). For our client from Pharmaceutical industry we automated
the data transfer from Clinical Study Protocol to Clinical Study Report.
Read Use Case→



The Pulse of A.I.


INTELLIGENT AUTOMATION IN HIGHLY REGULATED INDUSTRIES

We automate regulatory tasks and workflows along all areas of the product life
cycle. Our focus: MedTech, Pharmaceutical and Chemical industries.
Who we are→
Watch video
+


WHAT TOPICS MIGHT INTEREST YOU?

Reset all filters
All Industry MedTech Pharmaceutical Chemistry
All Expertises Regulatory Affairs Clinical Affairs Quality Management Risk
Management Medical Affairs Post-Market Surveillance Product Safety


YOUR SEARCH DID NOT MATCH

Unfortunately, there is no corresponding use case yet, but we can change that.
Do you have a process or workflow where you need support through intelligent
automation? Simply describe it and we will be happy to help you find a solution.

Our challenges are...*

Please select *
SalutationMrMrsDivers
First name, Last name *

Company *

Position in the company *

Phone * (für eventuelle Rückfragen)

E-Mail *

We look forward to writing the next success story with you.
I accept the Privacy Policy of the lexoro GmbH.*




BENEFITS FOR OUR CUSTOMERS

 * Reduction of costs
 * Increase of quality
 * Relief of employees
 * Experts with focus on their activities
 * Standardization of processes
 * Increase in productivity

Pharmaceutical
Regulatory AffairsRisk ManagementPost-Market SurveillanceProduct Safety


INTELLIGENT AUTOMATION FOR PHARMACOVIGILANCE

Drug Safety within the pharmaceutical industry is incredibly important and must
be monitored and tested on a regular basis. Intelligent Automation sup...
MedTechChemistryPharmaceutical
Quality ManagementRisk ManagementProduct Safety


AUTOMATION FOR QUALITY CONTROL – OOS & OOT

A globally active Pharmaceutical and Chemical substance producer and distributor
was interested in automating the mammoth task of Out-of-Specification...
Chemistry
Regulatory AffairsQuality ManagementProduct Safety


AUTOMATED CREATION OF CHEMICAL SAFETY REPORTS

lexoro has built a solution to automatically assemble and create Chemical Safety
Reports (CSR) with important chapters and tables. As the CSR is a vit...
MedTech
Regulatory AffairsQuality ManagementRisk ManagementPost-Market Surveillance


AUTOMATED POPULATION & CREATION OF THE SUMMARY OF SAFETY AND CLINICAL
PERFORMANCE

The Medical Device Regulation (MDR) has brought several obligations and
requirements regarding reporting, safety, and other risk-preventive actions.
T...
Chemistry
Regulatory AffairsQuality ManagementRisk ManagementProduct Safety


AUTOMATED CREATION OF DOCUMENTS AND POPULATION OF TABLES

For a globally active Chemical Group with decades of experience, lexoro
developed a solution that automatically creates documents and reports for the
...
Chemistry
Regulatory AffairsQuality ManagementRisk ManagementProduct Safety


CHEMICAL DATABASE SEARCH AND EVALUATION OF RESULTS

For a leading European provider of varnishes and paints, lexoro developed a
solution to automate the chemical database search and the evaluation of re...
Pharmaceutical
Regulatory AffairsRisk ManagementMedical Affairs


INTELLIGENT AUTOMATION FOR BENEFIT ASSESSMENT & AMNOG

For a leading European company providing medicines and care, lexoro developed a
solution to automate the benefit assessment for pharmaceuticals. By us...
Pharmaceutical
Regulatory AffairsMedical Affairs


AUTOMATED GENERATION OF OVERVIEWS AND SUMMARIES FOR CTD MODULE 2

Intelligent Automation is the key driver that not only accelerates the creation
and generation of CTD Module 2 Overviews and Summaries within a global...
MedTech
Regulatory AffairsClinical Affairs


AUTOMATED CREATION OF CLINICAL EVALUATION REPORTS

For one of the world’s leading medical technology companies which offers
innovative products and services in Medical and Surgical, Neurotechnolo...
PharmaceuticalMedTech
Regulatory AffairsQuality ManagementPost-Market Surveillance


AUTOMATED CREATION OF PSUR AND PMSR

For an innovative global healthcare company lexoro automated the creation of
Periodic Safety Update Reports (PSUR) and Post-Market Surveillance Report...
Pharmaceutical
Clinical AffairsMedical Affairs


AUTOMATED CREATION OF CLINICAL STUDY REPORTS

For one of the world’s leading research-driven pharmaceutical companies with 130
years of experience lexoro automated the creation of clinical s...
MedTech
Regulatory AffairsClinical Affairs


INTELLIGENT AUTOMATION FOR CLINICAL EVALUATION

For a leading European provider of system solutions for medicine and care lexoro
optimized the regular monitoring of medical devices with the applicat...
PharmaceuticalMedTech
Regulatory AffairsPost-Market Surveillance


AUTOMATION OF POST MARKET SURVEILLANCE PROCESSES

lexoro implemented Intelligent Automation to the post market surveillance
processes for a european-wide Pharmaceutical distributor, who’s produc...
Pharmaceutical
Quality Management


AUTOMATED CREATION OF PRODUCT QUALITY REVIEWS

The intelligent automation of the creation of product quality reviews for a
leading manufacturer of high-quality Pharmaceuticals was a challenge lexor...
Load more


THE LEXORO FOCUS

We have been working on the automation and digitization of critical business
processes for more than 20 years. In doing so, we have always focused on the
following triad: technical excellence (RPA and A.I.), process knowledge
(regulated workflows) and industry expertise (MedTech, Pharmaceutical,
Chemical).

Learn more


WE OFFER HIGH-IMPACT SOLUTIONS WITH A QUICK ROI


REDUCTION OF THE COSTS


QUALITY INCREASE


RELIEF FOR THE EMPLOYEES


EXPERTS FOCUSED ON THEIR ACTIVITIES


STANDARDI­ZATION OF PROCESSES


INCREASE PRODUCTIVITY


GET RID OF ROUTINE WORK?

Let´s talk about it. Our Solution Experts can give you further insight into
Intelligent Automation options along the entire Compliance-Chain.

Let BOTs and A.I. help you in time-consuming tasks and refocus your time on real
quality work.

Tell us about your wildest automation wishes – and we turn them into reality!

Check-In

Tell us about your problem

Please select *
SalutationMrMrsDivers
First name, Last name *

Company *

Position in the company *

E-Mail *

Phone

By submitting my application, I accept the electronic storage of my data in
compliance with the General Data Protection Regulation. The data will be deleted
automatically after 6 months.*




YOUR CONTACT PERSON

Sven Kolthof

Managing Director






SIGN UP TODAY FOR YOUR INITIAL BRAINSTORMING.

In this first, free Kickoff-Meeting we will briefly evaluate automation
potentials within your department and company – all in approx. 20 minutes.


INTELLIGENT AUTOMATION

AUTOMATION
RPA

ROBOTIC PROCESS AUTOMATION

Software Robots (BOTs) automate time-consuming, routine tasks along all stages
of the product life-cycle. Regulatory documents, reports and workflows are
integrated end-to-end across all enterprise platforms.

Read more about RPA

ARTIFICIAL INTELLIGENCE
NLP

NATURAL LANGUAGE PROCESSING

A.I. based technique that helps to understand the contents of documents,
including the contextual nuances of the language within them. The technology can
accurately extract, categorize and classify all kinds of regulatory related
contents.

Read more about NLP

NLG

NATURAL LANGUAGE GENERATION

NLG is a subfield of Artificial Intelligence and deals with the automated
generation of natural language texts through software. The technology can create
dossiers, studies, reports and compliance documents in all areas.

Read more about NLG

ISM

INDUSTRY SOLUTION MAPS

Solution Maps are task- and process-specific modules that integrate with
lexoro’s Intelligent Automation suite. The Solution Maps address all regulated
tasks, documents and reports along the industry-specific product life cycles.


ABOUT LEXORO

We automate your compliance projects along all stages of the product life cycle.
Our Solution Maps offer a suite of well designed use cases – centered all around
industry specific regulatory demands. From Regulatory Affairs and Clinical
Trials to Quality Management, Post-Market Surveillance and Risk Management. We
help you turn data from multiple sources into complete compliance solutions.
Fully automated. To speed up time to market.

Let BOTs do the routine work

Learn more


OUR PROCESS

Learn more about our process



 * Use Cases
 * Services

 * About Us
 * Career

 * Legal Notice
 * Privacy Policy

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