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Lorenz Life Sciences Group

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uuid000arq3

Namestring
Lorenz Life Sciences Group
Legal namestring
LORENZ Archiv-Systeme GmbH
Websiteurl
lorenz.cc
Company typeenum
Private
Founded yearint
1989
Descriptiontext

Lorenz Life Sciences Group (legal entity LORENZ Archiv-Systeme GmbH) is a privately held German software company founded in 1989 and headquartered in Frankfurt am Main, with 101-250 employees and wholly-owned subsidiaries including LORENZ Bridge Software GmbH and LORENZ Life Sciences GmbH. The company develops Regulatory Information Management (RIM) software for the life sciences industry, with core products including docuBridge (submission management and regulatory content management), eValidator (submission validation against health authority specifications), drugTrack (product information and lifecycle management, including IDMP/PMS and EUDAMED support), and Automator (business process automation), complemented by verifAI (an AI-assisted content validation add-on using Meta LLaMA 3 on AWS). The platform supports the full regulatory lifecycle from submission assembly through validation, publishing, and post-publishing activities, with deployment available via on-premise or LORENZ Cloud (Microsoft Azure, servers in Germany).

Lorenz serves two primary customer segments: pharmaceutical and biotech companies that compile and submit regulatory dossiers, and government health authorities that receive, validate, and review those submissions. The company reports 1,800+ paid installations across 48 countries and 19 health authorities in its installed base, including the US FDA, Health Canada, the Chinese NMPA, German BfArM, UK MHRA, Singapore HSA, and the European Directorate for the Quality of Medicines & Healthcare (EDQM). Distribution is primarily through direct enterprise sales supplemented by a regional partner network (e.g., Inpharmatis for Eastern Europe and Central Asia) and consortium models for national deployments (e.g., Singapore HSA with VRG and Websparks).

The company operates a subscription/enterprise licensing model with twice-yearly major releases and regulatory update packages, and revenue figures are not publicly disclosed. Marketing is centered on annual LORENZ Converge (in-person conference, Frankfurt 2026), LORENZ Connect (virtual conference reaching ~500 participants across 40 countries), the LORENZ TV video platform, and active LinkedIn and blog presence. The leadership team includes Wolfgang Witzel as President, Raoul-A. Lorenz as founder/legal representative, and Yaprak Eisinger as Managing Director for North America.

Short descriptiontext

Lorenz Life Sciences Group is a Frankfurt-based, privately held software company founded in 1989 that provides Regulatory Information Management (RIM) solutions — including docuBridge, eValidator, drugTrack, and Automator — to pharmaceutical companies and 19 health authorities worldwide, with 1,800+ installations across 48 countries.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
101–250
akta.pro rankint
HeadquartersFrankfurt, Germany
HQ citystring
Frankfurt
HQ countrystring
Germany
HQ regionstring
Europe
Markets served

Serves global market

Offices2 records

Each record includes

City, Country, Type, Description, Source

Keyword5 values
regulatory information management, eCTD submission software, pharmaceutical compliance solutions, regulatory validation software, IDMP lifecycle management
Industry2 codes
1Regulatory Information Management (RIM) & Submission Publishing Software
CodeHLAGAJALPrimaryYes
2Regulatory Operations & Publishing (eCTD, RIM, Submission Management)
CodeHLAGAKACPrimaryNo
NAICS code2 codes
  • Software Publishers5132
  • Other Scientific and Technical Consulting Services54169
SIC code1 code
  • Services-Commercial Physical & Biological Research8731
Product category
Life Sciences Regulatory Information Management Software
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model1 record
1Software Licensing and Subscription
TypeSubscription Recurring
Description

Enterprise software licensing model with major releases twice yearly (April and October) and minor releases. The company offers cloud and on-premise deployment options. Regulatory Update Packages address specification updates without full software updates.

lorenz.cc
Marketing channels8 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels4 records

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Personnel, Technology or R&D, Operations, Marketing or Sales, Infrastructure
GTM typeB2B
B2B
Offering typeSoftware
Software
Brand1 of 7 records shown
1LORENZ docuBridge
Description

Submission Management & Regulatory Content Management solution

lorenz.cc
+6 more records
Core offering1 text field

Lorenz Life Sciences Group develops and sells the LORENZ RIM (Regulatory Information Management) software platform used by pharmaceutical companies, biotech firms, and health authorities worldwide. Its core offerings are docuBridge for assembling, publishing, and managing eCTD regulatory submissions; eValidator for technical compliance validation of incoming submissions; and drugTrack for product information management, IDMP/PMS compliance, and EUDAMED medical device registration.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 of 3 values shown
  • 27% of world population receives new medicines approved through LORENZ solutions
+2 more records
Product overview1 text field

LORENZ Life Sciences Group offers a modular Regulatory Information Management (RIM) platform with core products including docuBridge (submission management and regulatory content management), eValidator (submission validation), and drugTrack (product information and lifecycle management). These are complemented by add-on modules such as Automator (business automation), verifAI (AI-powered validation), Content Validator, and EPIC (XEVMPD to PMS migration validation). The LORENZ RIM platform provides end-to-end regulatory operations support from submission assembly through validation, publishing, and post-publishing activities. The company serves both pharmaceutical industry and regulatory authorities, with solutions supporting eCTD standards, IDMP/PMS requirements, and EUDAMED compliance.

Product and service7 records
1LORENZ docuBridge
CategoryRegulatory Submission Management
Description

Submission Management and Regulatory Content Management solution used by pharmaceutical companies and health authorities to assemble, approve, publish, and submit regulatory dossiers in eCTD format, including eCTD 4.0 EU.

2LORENZ eValidator
CategoryRegulatory Submission Validation
Description

Submission validation solution that validates all incoming submissions for technical compliance against regulatory authority specifications.

3LORENZ drugTrack
CategoryRegulatory Product Information & Lifecycle Management
Description

Product Information and Lifecycle Management solution supporting IDMP compliance, PMS enrichment for EMA, EUDAMED registration for medical devices, and regulatory activity management.

4LORENZ Automator
CategoryRegulatory Workflow Automation
Description

Business automation solution that enables process automation and next-generation case management integration for regulatory workflows.

5LORENZ verifAI
CategoryAI-Powered Regulatory Validation
Description

AI-powered content validation tool that automates review processes by validating eCTD content for accuracy, completeness, and compliance using Meta LLaMA 3 hosted on AWS.

6LORENZ RIM
CategoryRegulatory Information Management Platform
Description

Comprehensive Regulatory Information Management platform encompassing submission management, regulatory content management, product information, lifecycle management, submission validation, and post-publishing capabilities.

7LORENZ EPIC (EV PMS Integrity Check)
CategoryRegulatory Data Migration Validation
Description

Validation tool for XEVMPD to PMS migration that provides automated comparison between systems, identifying discrepancies and data quality issues.

Scale indicator4 records

Each record includes

Type, Value, Description, Source

Partnership5 partners
Strategic tierCoreTypeChannel Partner/ Reseller/ DistributorAnnounced on2026-05-28
Description

Inpharmatis became an official LORENZ Partner authorized to promote and implement LORENZ RIM solutions (docuBridge, drugTrack, eValidator) for pharmaceutical companies in Turkey, Ukraine, Armenia, Azerbaijan, Belarus, Kazakhstan, Kyrgyzstan, Moldova, Tajikistan, Uzbekistan, Turkmenistan, Mongolia, Latvia, Lithuania, and Estonia. This partnership expands access to LORENZ solutions across Eastern Europe and Central Asia.

Strategic tierCoreTypeStrategic or Co-development PartnerAnnounced on2024-02-12
Description

Strategic partnership to offer Trusted Regulatory Spaces - secure, cloud-native environments for collaborative regulatory submission validation and scientific review. The partnership leverages DNAnexus precisionFDA platform and LORENZ eValidator for Project PRISM, a collaboration with FDA to demonstrate collaborative regulatory submission validation and review capabilities.

3precisionFDA (FDA/DNAnexus)
Strategic tierCoreTypeTechnology or Integration
Description

LORENZ eValidator is deployed on precisionFDA, FDA's production cloud platform built and powered by DNAnexus, enabling sponsors to share eCTD validation results with reviewers using Trusted Regulatory Spaces. This collaboration is part of Project PRISM with FDA and industry collaborators.

lorenz.cc
Strategic tierCoreTypeImplementation/ SI/ Consulting Partner
Description

Consortium partner with LORENZ and Websparks Pte. Ltd. for the Singapore HSA eCTD Reviewing Solution. VRG provides expertise for the implementation of the complete solution including docuBridge, eValidator, and Automator.

Strategic tierCoreTypeTechnology or Integration
Description

Consortium partner with LORENZ and VRG Pte. Ltd. for the Singapore HSA eCTD Reviewing Solution. Websparks provides the portal offering component of the complete eCTD solution.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight6 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Ennov provides a RIM, QMS, and document management suite targeting mid-market life sciences companies, with comparable eCTD publishing and submission management features to LORENZ.

TypeDirect peer
Description

EXTEDO (now part of PharmaLex/DocVerse) is a long-standing direct competitor in eCTD submission publishing and RIM, with comparable health authority and sponsor customer profiles.

TypeEmerging player
Description

PharmaLex (now part of Cencora) bundles regulatory consulting with the EXTEDO RIM platform, making it a peer in the combined software-plus-services regulatory value chain that LORENZ competes with.

TypeBroad incumbent
Description

IQVIA offers regulatory information management and RIM outsourcing as part of its broader clinical and commercialization technology stack. It competes with LORENZ for both sponsor and health authority business, and bundles RIM with adjacent CRO/CDM services.

TypeDirect peer
Description

ArisGlobal's LifeSphere RIM is a direct competitor to LORENZ's submission management, validation, and product information suite, targeting the same mid-to-large pharma market with a SaaS-first delivery model.

TypeEmerging player
Description

MasterControl provides quality management and regulatory document management solutions for life sciences. It overlaps with LORENZ on regulatory content management and GxP documentation but emphasizes QMS rather than submission publishing.

TypeDirect peer
Description

Amplexor (now part of Acolad) offers eCTD, RIM, and life sciences regulatory content solutions with a comparable feature footprint to LORENZ, serving pharma sponsors and health authorities across Europe.

TypeBroad incumbent
Description

Veeva's Vault RIM suite is the dominant cloud-native regulatory platform for large pharmaceutical sponsors. Veeva competes directly with LORENZ docuBridge/eValidator/drugTrack and has substantially greater scale and brand recognition in the same buyer segment.

TypeBroad incumbent
Description

Oracle's clinical and regulatory suite (including the former goBalto, Medidata, and Siebel CTMS assets) competes with LORENZ in the broader pharma software stack, particularly with large sponsors standardizing on Oracle Cloud.

TypeBroad incumbent
Description

DXC's life sciences practice offers regulatory information management and submission services as part of a broader IT services portfolio, competing with LORENZ particularly for large health authority transformation deals.

Market position
Strengths5 records

Each record includes

Headline, Details, Source

Weaknesses5 records

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Headline, Details, Source

Competitive moat5 records

Each record includes

Type, Details

Key risks5 records

Each record includes

Headline, Details, Source

Key highlights7 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers8 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile3 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
Yes

Docs URL, Description

Integration3 records

Each record includes

Title, Type, Description, Source

AI capability4 records

Each record includes

Type, Description, Source

AI maturity
App detail

Has app

Feature6 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

Subsidiaries2 records

Each record includes

Name, Acquired on, Relationship type, Type, Business focus

Compliance2 records

Each record includes

Name, Class, Description

Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Lorenz Life Sciences Group

Life Sciences Regulatory Information Management Softwarelorenz.cc

Lorenz Life Sciences Group is a Frankfurt-based, privately held software company founded in 1989 that provides Regulatory Information Management (RIM) solutions — including docuBridge, eValidator, drugTrack, and Automator — to pharmaceutical companies and 19 health authorities worldwide, with 1,800+ installations across 48 countries.

What Lorenz Life Sciences Group does

Lorenz Life Sciences Group (legal entity LORENZ Archiv-Systeme GmbH) is a privately held German software company founded in 1989 and headquartered in Frankfurt am Main, with 101-250 employees and wholly-owned subsidiaries including LORENZ Bridge Software GmbH and LORENZ Life Sciences GmbH. The company develops Regulatory Information Management (RIM) software for the life sciences industry, with core products including docuBridge (submission management and regulatory content management), eValidator (submission validation against health authority specifications), drugTrack (product information and lifecycle management, including IDMP/PMS and EUDAMED support), and Automator (business process automation), complemented by verifAI (an AI-assisted content validation add-on using Meta LLaMA 3 on AWS). The platform supports the full regulatory lifecycle from submission assembly through validation, publishing, and post-publishing activities, with deployment available via on-premise or LORENZ Cloud (Microsoft Azure, servers in Germany).

Lorenz serves two primary customer segments: pharmaceutical and biotech companies that compile and submit regulatory dossiers, and government health authorities that receive, validate, and review those submissions. The company reports 1,800+ paid installations across 48 countries and 19 health authorities in its installed base, including the US FDA, Health Canada, the Chinese NMPA, German BfArM, UK MHRA, Singapore HSA, and the European Directorate for the Quality of Medicines & Healthcare (EDQM). Distribution is primarily through direct enterprise sales supplemented by a regional partner network (e.g., Inpharmatis for Eastern Europe and Central Asia) and consortium models for national deployments (e.g., Singapore HSA with VRG and Websparks).

The company operates a subscription/enterprise licensing model with twice-yearly major releases and regulatory update packages, and revenue figures are not publicly disclosed. Marketing is centered on annual LORENZ Converge (in-person conference, Frankfurt 2026), LORENZ Connect (virtual conference reaching ~500 participants across 40 countries), the LORENZ TV video platform, and active LinkedIn and blog presence. The leadership team includes Wolfgang Witzel as President, Raoul-A. Lorenz as founder/legal representative, and Yaprak Eisinger as Managing Director for North America.

Lorenz Life Sciences Group firmographics

Firmographics
Name
Lorenz Life Sciences Group
Legal name
LORENZ Archiv-Systeme GmbH
Website
https://lorenz.cc
Company type
Private
Founded year
1989
Operating status
Operating
Headcount range
101–250 employees
Short description
Lorenz Life Sciences Group is a Frankfurt-based, privately held software company founded in 1989 that provides Regulatory Information Management (RIM) solutions — including docuBridge, eValidator, drugTrack, and Automator — to pharmaceutical companies and 19 health authorities worldwide, with 1,800+ installations across 48 countries.
Ownership category
akta.pro rank

Lorenz Life Sciences Group industry classification

Industry
Product category
Life Sciences Regulatory Information Management Software
NAICS
Software Publishers (5132), Other Scientific and Technical Consulting Services (54169)
SIC
Services-Commercial Physical & Biological Research (8731)
akta.pro primary industry
Regulatory Information Management (RIM) & Submission Publishing Software (HLAGAJAL)
akta.pro secondary industry
Regulatory Operations & Publishing (eCTD, RIM, Submission Management) (HLAGAKAC)

Keywords

  • Regulatory information management
  • ECTD submission software
  • Pharmaceutical compliance solutions
  • Regulatory validation software
  • IDMP lifecycle management

Where Lorenz Life Sciences Group is headquartered

Location

Headquarters

HQ city
Frankfurt
HQ country
Germany
HQ region
Europe

Offices2 records

Markets served

Lorenz Life Sciences Group business model

Business model
GTM type
B2B
Offering type
Software
Cost components
Personnel, Technology or R&D, Operations, Marketing or Sales, Infrastructure

Revenue model

  1. Software Licensing and Subscription: Enterprise software licensing model with major releases twice yearly (April and October) and minor releases. The company offers cloud and on-premise deployment options. Regulatory Update Packages address specification updates without full software updates.

Go-to-market motion1 record

Distribution channels4 records

Marketing channels8 records

Lorenz Life Sciences Group product offering

Product offering

Core offering

Lorenz Life Sciences Group develops and sells the LORENZ RIM (Regulatory Information Management) software platform used by pharmaceutical companies, biotech firms, and health authorities worldwide. Its core offerings are docuBridge for assembling, publishing, and managing eCTD regulatory submissions; eValidator for technical compliance validation of incoming submissions; and drugTrack for product information management, IDMP/PMS compliance, and EUDAMED medical device registration.

Product overview

LORENZ Life Sciences Group offers a modular Regulatory Information Management (RIM) platform with core products including docuBridge (submission management and regulatory content management), eValidator (submission validation), and drugTrack (product information and lifecycle management). These are complemented by add-on modules such as Automator (business automation), verifAI (AI-powered validation), Content Validator, and EPIC (XEVMPD to PMS migration validation). The LORENZ RIM platform provides end-to-end regulatory operations support from submission assembly through validation, publishing, and post-publishing activities. The company serves both pharmaceutical industry and regulatory authorities, with solutions supporting eCTD standards, IDMP/PMS requirements, and EUDAMED compliance.

Differentiator

Problem solved

Functional benefit

Brands

  • LORENZ docuBridge: Submission Management & Regulatory Content Management solution
  • LORENZ eValidator
  • LORENZ drugTrack
  • LORENZ Automator
  • LORENZ verifAI
  • LORENZ EPIC
  • LORENZ RIM

Products and services

  • LORENZ docuBridge Submission Management and Regulatory Content Management solution used by pharmaceutical companies and health authorities to assemble, approve, publish, and submit regulatory dossiers in eCTD format, including eCTD 4.0 EU.
  • LORENZ eValidator Submission validation solution that validates all incoming submissions for technical compliance against regulatory authority specifications.
  • LORENZ drugTrack Product Information and Lifecycle Management solution supporting IDMP compliance, PMS enrichment for EMA, EUDAMED registration for medical devices, and regulatory activity management.
  • LORENZ Automator Business automation solution that enables process automation and next-generation case management integration for regulatory workflows.
  • LORENZ verifAI AI-powered content validation tool that automates review processes by validating eCTD content for accuracy, completeness, and compliance using Meta LLaMA 3 hosted on AWS.
  • LORENZ RIM Comprehensive Regulatory Information Management platform encompassing submission management, regulatory content management, product information, lifecycle management, submission validation, and post-publishing capabilities.
  • LORENZ EPIC (EV PMS Integrity Check) Validation tool for XEVMPD to PMS migration that provides automated comparison between systems, identifying discrepancies and data quality issues.

Quantifiable outcome

  • 27% of world population receives new medicines approved through LORENZ solutions
  • +2 more outcomes

Companies that use Lorenz Life Sciences Group

Customer profile

Named customers8 records

Segments3 records

Ideal customer profiles3 records

Lorenz Life Sciences Group technology and API

Technology

Technology focussed Yes

API detail

Has API
Yes
API docs
API detail

Core technology

AI maturity

App detail

Integration3 records

AI capability4 records

Feature6 records

Lorenz Life Sciences Group partnerships and signals

Strategic signal

Partnerships

Five partnerships are on record, tiered core.

  • InpharmatiscoreChannel Partner/ Reseller/ Distributor · 28 May 2026Inpharmatis became an official LORENZ Partner authorized to promote and implement LORENZ RIM solutions (docuBridge, drugTrack, eValidator) for pharmaceutical companies in Turkey, Ukraine, Armenia, Azerbaijan, Belarus, Kazakhstan, Kyrgyzstan, Moldova, Tajikistan, Uzbekistan, Turkmenistan, Mongolia, Latvia, Lithuania, and Estonia. This partnership expands access to LORENZ solutions across Eastern Europe and Central Asia.
  • DNAnexuscoreStrategic or Co-development Partner · 12 February 2024Strategic partnership to offer Trusted Regulatory Spaces - secure, cloud-native environments for collaborative regulatory submission validation and scientific review. The partnership leverages DNAnexus precisionFDA platform and LORENZ eValidator for Project PRISM, a collaboration with FDA to demonstrate collaborative regulatory submission validation and review capabilities.
  • precisionFDA (FDA/DNAnexus)coreTechnology or IntegrationLORENZ eValidator is deployed on precisionFDA, FDA's production cloud platform built and powered by DNAnexus, enabling sponsors to share eCTD validation results with reviewers using Trusted Regulatory Spaces. This collaboration is part of Project PRISM with FDA and industry collaborators.
  • VRG Pte. Ltd.coreImplementation/ SI/ Consulting PartnerConsortium partner with LORENZ and Websparks Pte. Ltd. for the Singapore HSA eCTD Reviewing Solution. VRG provides expertise for the implementation of the complete solution including docuBridge, eValidator, and Automator.
  • Websparks Pte. Ltd.coreTechnology or IntegrationConsortium partner with LORENZ and VRG Pte. Ltd. for the Singapore HSA eCTD Reviewing Solution. Websparks provides the portal offering component of the complete eCTD solution.

Scale indicators4 records

Recent moves6 records

Expansion highlights6 records

Lorenz Life Sciences Group competitors and assessment

Company assessment

Direct peers

  • Ennov: Ennov provides a RIM, QMS, and document management suite targeting mid-market life sciences companies, with comparable eCTD publishing and submission management features to LORENZ.
  • EXTEDO: EXTEDO (now part of PharmaLex/DocVerse) is a long-standing direct competitor in eCTD submission publishing and RIM, with comparable health authority and sponsor customer profiles.
  • ArisGlobal: ArisGlobal's LifeSphere RIM is a direct competitor to LORENZ's submission management, validation, and product information suite, targeting the same mid-to-large pharma market with a SaaS-first delivery model.
  • Amplexor (Acolad Life Sciences): Amplexor (now part of Acolad) offers eCTD, RIM, and life sciences regulatory content solutions with a comparable feature footprint to LORENZ, serving pharma sponsors and health authorities across Europe.

Emerging players

  • PharmaLex (Cencora): PharmaLex (now part of Cencora) bundles regulatory consulting with the EXTEDO RIM platform, making it a peer in the combined software-plus-services regulatory value chain that LORENZ competes with.
  • MasterControl: MasterControl provides quality management and regulatory document management solutions for life sciences. It overlaps with LORENZ on regulatory content management and GxP documentation but emphasizes QMS rather than submission publishing.

Broad incumbents

  • IQVIA: IQVIA offers regulatory information management and RIM outsourcing as part of its broader clinical and commercialization technology stack. It competes with LORENZ for both sponsor and health authority business, and bundles RIM with adjacent CRO/CDM services.
  • Veeva Systems: Veeva's Vault RIM suite is the dominant cloud-native regulatory platform for large pharmaceutical sponsors. Veeva competes directly with LORENZ docuBridge/eValidator/drugTrack and has substantially greater scale and brand recognition in the same buyer segment.
  • Oracle Health Sciences (formerly Oracle Argus/Inform): Oracle's clinical and regulatory suite (including the former goBalto, Medidata, and Siebel CTMS assets) competes with LORENZ in the broader pharma software stack, particularly with large sponsors standardizing on Oracle Cloud.
  • DXC Technology (formerly CSC Life Sciences): DXC's life sciences practice offers regulatory information management and submission services as part of a broader IT services portfolio, competing with LORENZ particularly for large health authority transformation deals.

Market position

Strengths5 records

Weaknesses5 records

Competitive moat5 records

Key risks5 records

Key highlights7 records

Customer concentration

Lorenz Life Sciences Group social profiles

Digital presence

Lorenz Life Sciences Group compliance and trust

Trust signal

Compliance2 records

Lorenz Life Sciences Group financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Lorenz Life Sciences Group leadership team

Management profile

Number of profiles

Profiles3 records

Lorenz Life Sciences Group subsidiaries and ownership

Company hierarchy

Subsidiaries2 records

Lorenz Life Sciences Group funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Lorenz Life Sciences Group M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Lorenz Life Sciences Group

What does Lorenz Life Sciences Group do?

Lorenz Life Sciences Group develops and sells the LORENZ RIM (Regulatory Information Management) software platform used by pharmaceutical companies, biotech firms, and health authorities worldwide. Its core offerings are docuBridge for assembling, publishing, and managing eCTD regulatory submissions; eValidator for technical compliance validation of incoming submissions; and drugTrack for product information management, IDMP/PMS compliance, and EUDAMED medical device registration.

Is Lorenz Life Sciences Group a public or private company?

Lorenz Life Sciences Group is a private company. It is classified as founder individual operated bootstrapped and is currently operating.

When was Lorenz Life Sciences Group founded?

Lorenz Life Sciences Group was founded in 1989. It employs 101 to 250 people.

Where is Lorenz Life Sciences Group based?

Lorenz Life Sciences Group is headquartered in Frankfurt, Germany, in the Europe region.

How does Lorenz Life Sciences Group make money?

One revenue line is on record: software Licensing and Subscription.

Who are Lorenz Life Sciences Group's main competitors?

Direct peers on record are Ennov, EXTEDO, ArisGlobal and Amplexor (Acolad Life Sciences). Emerging players are PharmaLex (Cencora) and MasterControl. Broad incumbents are IQVIA, Veeva Systems, Oracle Health Sciences (formerly Oracle Argus/Inform) and DXC Technology (formerly CSC Life Sciences).

Does Lorenz Life Sciences Group have an API?

Yes. LORENZ provides PMS (Product Management Service) API Write Access for EMA's PMS system, enabling direct data enrichment submissions to EMA's PMS Production system without manual data entry. This API allows authorized users to validate, enrich, and update PMS data directly from within drugTrack. The PMS API Write Access has been live since September 25, 2025.

What industry is Lorenz Life Sciences Group in?

Lorenz Life Sciences Group's product category is Life Sciences Regulatory Information Management Software. Its primary akta.pro industry code is HLAGAJAL, Regulatory Information Management (RIM) & Submission Publishing Software, with a secondary code of HLAGAKAC, Regulatory Operations & Publishing (eCTD, RIM, Submission Management). Its NAICS code is 5132 and its SIC code is 8731.

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Live signals
PR NewswireLORENZ docuBridge, eValidator, and Automator go live at the USFDAThe U.S. Food and Drug Administration has gone live with LORENZ Life Sciences Group's docuBridge and eValidator solutions, with the Center for Drug Evaluation and Research (CDER) and Center for Biologics Evaluation and Research (CBER) now using these tools to process incoming and legacy regulatory submissions. The implementation concluded a four-year procurement process that began in 2016, involving migration of 1.2 million legacy sequences and 1.5 million total sequences, completed in just 16 days, with over 4,000 reviewers trained virtually during the COVID-19 pandemic. The go-live enables a seamless submission process for companies using LORENZ docuBridge and establishes closer collaboration between LORENZ and the USFDA on eCTD 4.0.PR NewswireAlliance of Experts: Your partner for an end-to-end RIM solution in Life SciencesGeneris, Phlexglobal, and LORENZ Life Sciences Group announced the founding of the Alliance of Experts on February 12, 2019, a partnership providing end-to-end Regulatory Information Management (RIM) and Clinical solutions for the Life Sciences industry. The alliance integrates each company's software to offer customers a unified solution with guaranteed interoperability between applications. The companies claim this approach eliminates the burden of maintaining multiple disconnected tools while providing deeper functionality than traditional single-vendor or multi-specialist approaches.GlobeNewswireMasterControl and LORENZ Life Sciences Group Celebrate Decade Long Partnership and Integration in Streamlining eCTD SubmissionsMasterControl and LORENZ Life Sciences Group announced a decade-long partnership integrating LORENZ docuBridge with MasterControl v11.6. The integration allows drag-and-drop document management for eCTD submissions, with new APIs enabling automatic population of eCTD attributes. LORENZ docuBridge is FDA-approved for eCTD validation and review.PR NewswireFDA awards LORENZ eCTD ContractThe U.S. Food and Drug Administration (FDA) awarded LORENZ Life Sciences Group a contract for eCTD validation and review software on September 30, 2016. LORENZ will implement its docuBridge, eValidator, and Automator solutions within the FDA's Center for Drug Evaluation and Research (CDER) and Center for Biologics Evaluation and Research (CBER). The partnership aims to validate and review incoming and legacy electronic submissions.