Life Sciences — IBU

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Life Sciences

Accelerating drug development and patient outcomes through technology

IBU partners with pharmaceutical companies, biotech firms, CROs and medical device manufacturers to modernise clinical trial management, automate regulatory submissions, strengthen pharmacovigilance, and deploy AI-driven drug discovery platforms.

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Overview

The Sector Challenge

Life sciences companies face intense pressure to reduce time-to-market for new therapies, meet evolving FDA, EMA and MHRA requirements, and harness the power of real-world data and AI. IBU brings deep expertise across the drug development lifecycle — from discovery and clinical trials through to commercial launch and post-market surveillance — helping organisations accelerate innovation while maintaining the highest standards of data integrity and regulatory compliance.

Key Challenges

What We Solve

  • Clinical trial management system (CTMS) modernisation
  • Regulatory submission automation (eCTD, IDMP)
  • Pharmacovigilance and adverse event reporting
  • Real-world data and evidence generation
  • AI-assisted drug discovery and target identification
  • GxP compliance and data integrity
  • Laboratory information management (LIMS) integration
  • Supply chain serialisation and track-and-trace
  • Commercial launch analytics and market access
  • Medical device software (SaMD) development
What We Do

Our Capabilities in Life Sciences

01Clinical Trial Management System (CTMS)
02Regulatory Submission Automation (eCTD/IDMP)
03Pharmacovigilance & Adverse Event Platforms
04Real-World Data & Evidence Analytics
05AI Drug Discovery & Target Identification
06GxP Compliance & Data Integrity Frameworks
07LIMS Integration & Laboratory Digitalisation
08Supply Chain Serialisation & Track-and-Trace
09Commercial Analytics & Market Access
10Medical Device Software (SaMD) Development
11Patient Engagement & Decentralised Trials
12Healthcare Interoperability (HL7 FHIR)
Value Delivered

Business Outcomes

Faster Trial Execution

Integrated CTMS and eTMF platforms reduce trial start-up times and improve site performance monitoring.

Regulatory Confidence

Automated eCTD compilation and IDMP data standards reduce submission errors and accelerate agency review.

Data Integrity

GxP-validated systems and audit trail frameworks ensure data integrity across the full development lifecycle.

AI-Accelerated Discovery

Machine learning models for target identification and compound screening compress early-stage discovery timelines.

Patient Safety

Real-time pharmacovigilance platforms detect safety signals earlier and automate expedited reporting obligations.

Commercial Readiness

Launch analytics and market access platforms support pricing, reimbursement and commercial performance tracking.

Case Studies

Client Impact

01

CTMS Implementation

Deployed a global CTMS for a top-10 pharmaceutical company, consolidating 14 legacy systems and improving trial milestone visibility across 60 countries.

02

Pharmacovigilance Automation

Automated adverse event intake and MedDRA coding for a mid-size biotech, reducing case processing time by 55% and eliminating late submissions.

03

AI Drug Discovery Platform

Built an AI-assisted target identification platform for a biotech firm, shortlisting viable drug candidates 3x faster than traditional screening methods.

04

SaMD Development

Developed and CE-marked a Class IIa medical device software for AI-assisted ECG interpretation, meeting MDR 2017/745 requirements throughout.

Ready to transform your life sciences operations?

Speak with an IBU specialist who understands your sector's unique pressures and opportunities.

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