Useful real-world technology solutions to common manual processes.

PLG is building a dream AI/digital toolset for life science professionals, eliminating the manual drudgery and potential for errors so you can focus on bringing greater human expertise to your daily processes. Many of the below products and services are beyond proof of concept and already in production or validated and service ready.  

Regulatory Affairs / RIM 

IDMP Analytics & Readiness: 

  • Extracts, structures, and assesses product data across regulatory sources to identify IDMP gaps and readiness issues 
  • Reduces manual effort, improves data quality and readiness, and accelerates IDMP preparation and enrichment. 

 

Shortage Management Plan Product Data Autofill App: 

  • Automatically populate product templates using CIS code-based data retrieval and structured information filling 
  • Reduces manual data entry, accelerates document preparation, and improves data consistency 

 

Personalized Regulatory Intelligence Newsletter: 

  • Aggregate and analyse regulatory news and updates (e.g. EMA, FDA, NHS) across multiple sources to generate personalized newsletters based on user-defined scope of interest 
  • Reduces manual monitoring effort, improves awareness of regulatory changes, and delivers targeted, actionable insights for faster decision-making 

Document Classifier

Automatically classifies documents according to predefined taxonomies (e.g. Veeva/RIM), document types or target repositories. 

Reduces manual classification effort, improves consistency during document migration or repository structuring, and supports cleaner metadata and downstream process automation. 

Pharmacovigilance / Safety

AI-Powered Literature Automation Screening & Classification: 

  • Manage literature intake, classification, reporting and KPI tracking in a unified workflow 
  • Reduces manual workload and standardizes monitoring processes 

PV Case Translation Service: 

  • Translate local safety cases for centralized intake and processing 
  • Speeds up global case processing and reduce costs 

RIM / Clinical / Quality / Safety

Validated Migration Service: 

  • Full Validated ETL process performing controlled migration of data into any target system 
  • Enables go-live with data from an outgoing system 
  • Accelerates go to market time following a merger or acquisition 

Translation / Labelling / Publishing

AI Translation Platform (Universal RA Translator): 

  • Submit, translate, validate and manage regulated multilingual content through a controlled workflow 
  • Reduce translation cost and cycle time while ensuring consistency, compliance and improved quality 

Advanced Translation Output Service: 

  • Translate text embedded in images or scanned content and regenerate final documents while preserving original formatting and structure across outputs such as PDF, DOCX and PPTX 
  • Extends translation coverage to non-editable content, reduces post-translation rework, and accelerates delivery of publication-ready multilingual documents 

eCTD Publishing Automation: 

  • Prepare, validate and manage eCTD submissions with automated checks and collaboration 
  • Improves submission quality and reduces manual publishing effort and error risk 

3D PI Leaflet: 

  • Deliver interactive digital product information content for patients and healthcare professionals. 
  • Modernizes patient communication, improves accessibility, and supports enhances engagement with product information. 

Medical Devices / Business Development

EUDAMED Data Extractor: 

  • Extract and structure target company and device information from EUDAMED to support lead generation, segmentation, market analysis and expert review 
  • Automates manual list building, improves target identification, supports new business opportunities, and creates reusable medical device intelligence for both sales and SME teams 

Integration / Administration

Veeva User Management: 

  • Manage user lifecycle, roles, approvals and provisioning for Veeva 
  • Streamlines onboarding/offboarding, enforces access policies and improves auditability 

Quality & Compliance

GDP Qualification Automation: 

  • Automate customer qualification workflows using AI to process and assess large customer databases in line with regulatory requirements 
  • Reduces qualification effort by up to 65%, reducing processing time from 5-10 minutes per customer line to ~30 seconds 
  • Lowers operational cost while supporting scalable, compliant qualification 

GxP AI Validation & Compliance Advisory: 

  • Define and implement a methodological framework ensuring GxP adherence for digital solutions embedding state-of-the-art LLM and AI workflows 
  • Enables safe AI adoption in regulated environments 
  • Reduces compliance risk and ensures audit-ready, traceable deployments 

PQR Compliance Analyzer: 

  • Analyse Product Quality Review (PQR) documents and annexes against GMP (BPF) regulatory requirements 
  • Prefill structured evaluation forms, detect missing or undocumented elements, and identify inconsistencies including between textual and graphical data, with human validation through a dedicated platform 
  • Reduces manual review effort while improving compliance coverage 
  • Detect inconsistencies early and accelerate the preparation of audit-ready PQR evaluations 

 

PLG combines its extensive domain expertise with AI/automation and compliant delivery to help life science teams modernise manual processes. This approach ensures the high quality, traceability, and oversight required in regulated GxP environments.  

We don’t just automate tasks, we provide validated and scalable digital solutions that help industry experts make faster, better, and safer decisions.