---
name: The Micron Group
slug: micron-group
site: cro
website_domain: micron-group.com
summary: Global CRO delivering clinical trial management, regulatory consultancy, data management, and medical writing for biotech, pharma, and medical device companies across Phase I–IV studies and real-world evidence programs. Headquartered in Ely, United Kingdom.
tagline: Proven, dedicated CRO for biotech, pharma, and medical device trials with global reach and local focus.
founded_year: 1996
employee_count_band: 
employee_count_label: 
parent_name: 
parent_slug: 
hq_country: GB
tier2_domain_verified: false
updated_at: 2026-08-23T07:06:31.859Z
services_count: 11
modalities_count: 0
indications_count: 1
locations_count: 5
review_signal_gate: closed
generated_by: BioBM Editorial AI
---

# The Micron Group

Proven, dedicated CRO for biotech, pharma, and medical device trials with global reach and local focus.

Listed on cro.directory.

## Summary

Global CRO delivering clinical trial management, regulatory consultancy, data management, and medical writing for biotech, pharma, and medical device companies across Phase I–IV studies and real-world evidence programs. Headquartered in Ely, United Kingdom.

## At a glance

- Founded: 1996
- HQ country: GB

## Services

- Phase I Clinical Trials
- Phase II Clinical Trials
- Phase III Clinical Trials
- Phase IV / Post-Marketing
- Clinical Operations
- Data Management & eClinical
- Medical Writing
- Regulatory Affairs
- US FDA Regulatory Strategy
- EU EMA Regulatory Strategy
- Device & Combination Product Services

## Indications

- Infectious Disease

## Locations

- Headquarters, Ely, Cambridgeshire, United Kingdom
- US Micron, Overland Park, Kansas, United States
- EU Micron, Tallinn, Harju maakond, Estonia
- Clindev, Centurion, Irene, South Africa
- LogicTrials, Centurion, Irene, South Africa

## Long description

The Micron Group is a specialist Contract Research Organization (CRO) providing high-quality clinical trial support for biotech, pharmaceutical, and medical device companies. The organization delivers tailored solutions for Phase I to Phase IV studies, real-world evidence programs, and post-marketing research with emphasis on regulatory compliance, global coordination, and regional expertise.

## Core Services

- **Integrated Clinical Development:** On-site and remote clinical monitoring services, risk-based monitoring (RBM), oversight monitoring of other CROs, and end-to-end support from protocol to submission
- **Regulatory Support:** In-depth knowledge of ICH-GCP guidelines and evolving global regulatory requirements; expertise in gaining rapid health authority approvals
- **Data Management Services:** Secure, scalable data management built for clinical accuracy
- **Medical Writing and Communications:** Clear, compliant, publication-ready outputs
- **Consultancy:** Expert guidance from discovery through commercial stages
- **Drug Distribution and Logistics:** Clinical trial and commercial distribution services
- **Software Solutions:** Data analytics platforms and education software
- **Capacity Development:** Healthcare capacity building through training and infrastructure support across the United States, United Kingdom, and multiple African regions

## Therapeutic Area Expertise

Clinical research professionals have expertise across multiple therapeutic areas, with particular focus on infectious diseases (including involvement in the P-PEAKS phage therapy consortium for drug-resistant infections).

## Global Presence

Offices in the UK (Ely, Cambridgeshire), USA (Overland Park, Kansas), EU (Tallinn, Estonia), and South Africa (Centurion), enabling local expertise with global coordination.

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_Profile last updated: 2026-08-23T07:06:31.859Z. Profile facts may include AI-assisted enrichment._

Auto-generated by BioBM Editorial AI for machine-readable profile access.