Your challenge.
Our CRO Expertise.

One goal:
Fast-track your drug development.

Evidenze is a leading global CRO specializing in Biotechs and Small & Medium Pharma or MedTech companies seeking a strategic partner for their clinical development, delivering full value at every stage of the process.

CLINICAL RESEARCH REPORT | JULY 2025

Navigating early-phase trials: a regulatory survival guide for biotech

Designed for
Smart Research.

Our company is committed to supporting the needs of Biotech and Small to Mid-sized Pharma companies by integrating scientific expertise, regulatory compliance, operational excellence, and strong connections with research sites and KOLs to optimize patient recruitment and ensure the successful execution of clinical studies.

Deep scientific expertise in your therapeutic area. Regulatory expertise to navigate every step. Agile operations: flexible, scalable, and efficient. A powerful network of research sites and KOLs.
Deep scientific expertise in your therapeutic area. Regulatory expertise to navigate every step. Agile operations: flexible, scalable, and efficient. A powerful network of research sites and KOLs.

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Solutions Built Around Your Needs.

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At Evidenze CRO, we understand that no two companies are the same. That’s why we tailor our support to fit your goals, your resources, and your timelines—whether you're scaling fast or tackling complex regulatory landscapes.

Let us turn your challenge into progress.

CRO Full
value
services

Diagram showing core services of a clinical research organization. At the center is the company logo, connected by arrows to seven surrounding services: Start-up Regulatory, Medical Writing, Project Management, Pharmacovigilance, Data Management & Biostatistics, Technology Resources, and Clinical Operations.
  1. Scientific Advisory & Medical Writing
  2. Study start-up & regulatory
  3. eCRF, ePRO, eConsent, eRND, telemedicine programming
  4. Project Management
  5. Monitoring (on-site, remote)
  6. Data Management & Biostatistics
  7. Clinical reports and interpretation of results
  8. Scientific communications
  9. Pharmacovigilance
  10. Natural Language Processing from Electronic Medical Records
  11. Resourcing solutions
  12. Home care solutions
Diagram showing core services of a clinical research organization. At the center is the company logo, connected by arrows to seven surrounding services: Start-up Regulatory, Medical Writing, Project Management, Pharmacovigilance, Data Management & Biostatistics, Technology Resources, and Clinical Operations.>

Your needs
in Europe.

Our capabilities.

+14 countries where we operate. +450 Professional team especialized in clinical research. +25 Years of experience in clinical research. ISO 9001:2015 for Research and PSP. Strong Digital health solutions. +14 countries where we operate. +450 Professional team especialized in clinical research. +25 Years of experience in clinical research. ISO 9001:2015 for Research and PSP. Strong Digital health solutions.

Key activities
performed per year

0

Approvals by Healthcare Autorities

0

ECs submissions

0

Sites contracts managed

0

Monitoring visits conducted

0

Statistical Analysis/reports

0

Scientific writing documents

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Wide experience in different
therapeutic areas.

Oncology



Click or tap Click on your area of interest

Clinical research reports

CLINICAL RESEARCH REPORT - JULY 2025
Navigating Early-Phase Trials: A Regulatory Survival Guide for Biotech

ESG Commitment is a Foundational Pillar Underpinning Quality Services and Operational Excellence

ESG Commitment is a Foundational Pillar Underpinning
Quality Services and Operational Excellence

ESG Overview

Evidenze is fully committed to integrating Environmental, Social, and Governance (ESG) principles into every aspect of its operations.

The Group aims to reduce resource consumption through digitalization and energy-efficient measures.

Policies are advanced to promote work-life balance and equal opportunities for all employees.

Comprehensive safety measures are implemented, with continuous input gathered from employees through engagement surveys.

Supplier compliance with safety and ethical standards is ensured.

ISO-certified processes are implemented to maintain the highest standards of safety and quality across its programs.

ISO 9001:2015 certification. Evidence obtained ISO 9001 for quality management in the Patient Support Programs business.
ISO 9001:2015 certification. Evidence obtained ISO 9001 for quality management in the Clinical Research business.
Ecovadis sustainability rating. Evidencee and its subsidiaries are listed individually and updated annually. Evidence holds Ecovadis Platinum rating in Germany.

Standard Programs and Initiatives

Environmental

Objective to decrease energy and paper consumption by implementing digital processes and energy-efficient technologies

Registered with ECOVADIS to evaluate and benchmark our performance in sustainable development and corporate social responsibility

Social

Developing and communicating new employee policies throughout 2024, including a 'Right to Disconnect' protocol and a flexible working policy 

Updating the Gender Equality Plan to be signed with the Works Council, ensuring equal opportunities for all employees

Conducting an engagement survey to assess employee satisfaction and identify areas for improvement in health and well-being

Engaged in pro-bono projects across business units leveraging unique know-how and capabilities

Governance

Established an internal whistleblower channel to encourage confidential reporting of safety concerns and unethical practices

Conducted comprehensive cyber-security training to safeguard company data and prevent breaches

Implemented supplier homologation processes to ensure compliance with safety and ethical standards across the supply chain

Adopted an ethics code that includes a strict anti-corruption and bribery policy to maintain transparency and integrity