Our concept: Agile and specialized
with one contact person
- From study design to publication - you decide, we support. We accompany you through every stage of your project, tailoring our support to your needs.
- Direct contact, no delays. You always reach your dedicated contact person quickly - without waiting loops or ticket systems.
- Our specialists work to the highest quality standards - and contribute not only their expertise and reliability, but also genuine dedication to the success of your project.
Summary
Mediconomics is a leading contract research organization (CRO) and pharmaceutical consultant for research and development projects of pharmaceuticals and medical devices.
Headquartered in Hanover, Germany, with offices in Denmark, Switzerland, the UK and the USA, Mediconomics operates within an international network and ensure full compliance with evolving regulatory requirements.
Quality management is one of the foundations of our success. The members of our interdisciplinary team are continuously trained in accordance with the latest and highest standards. We also maintain a certified quality management system in accordance with DIN EN ISO 9001:2015
With more than 25 years of experience and long-standing customer relationships, we follow a core philosophy: to remain small enough to deliver flexible, tailored solutions, yet large enough to manage complex situations.
Since 1999, Mediconomics has been recognized for its systematic and individual approach- and we would be delighted to contribute our expertise to your next project.
Management
Dr. (MD) Uwe Albrecht,
FIBMS, FFPM (Dis.), FICR, CSci
Managing Director
Following several years in senior positions in a globally active CRO in England, he took over the German branch in the late 1990s, an organization which at that time could already look back on 20 years of expertise. Prior to this, he was Director of Infectiology and Oncology at a leading international pharmaceutical company.
His vision of an agile yet comprehensive consulting– “small enough for flexible solutions, big enough for complex situations” – remains central to our corporate culture today. Beyond his role as Managing Director, he continues to act as clinical project manager in selected projects, ensuring clients benefit directly from his deep expertise in clinical research, regulatory affairs, medical writing, and product development.
His contributions are recognized internationally, and he has been named a Fellow of the Faculty of Pharmaceutical Medicine of the Royal College of Physicians (UK), the Institute of Biomedical Science, and the Institute for Clinical Research.
Nykøbing F, Denmark
Hanover, Germany
Founded and head office since 1999
Goring On Thames, United Kingdom
Olten, Switzerland
Los Angeles CA, USA
Affiliated companies
Mediconomics has not been operating alone for a long time, but has spun off further specialized sub-areas into separate sister companies. These include an MDR-compliant medical device manufacturer that is certified by a notified body and, in the context of clinical trials, a site management organization that enables sponsors to process trial contracts and invoices centrally.
Medicoforum GmbH
Medicoforum, based in Hanover, is a well-established consulting company specializing in regulatory services for the certification of medical devices in accordance with the Medical Device Regulation (MDR). As a reliable partner, we support manufacturers in the preparation of the complete range of technical and clinical documentation – from clinical evaluation (CER) and biological evaluation (BER) to post-market clinical follow-up (PMCF) and risk management.
Our services provide targeted support to meet regulatory requirements in an efficient, legally compliant and practical manner. Beyond MDR certification, the team also assists with the establishment, further development and maintenance of quality management systems –in full accordance with international standards such as ISO 13485.
As part of an international network of experienced partner organizations worldwide – Medicoforum combines regulatory expertise with a deep understanding of the market. This enables our sister company to seamlessly integrate regulatory requirements into your product development and significantly accelerate time to market approval.
Medicoscience GmbH
Medicoscience is a provider of services related to the administration of clinical trials for medicinal products, medical devices and in-vitro diagnostics (IVD). The highly regulated nature of clinical research requires rigorous administration, robust quality assurance and strict data protection. Medicoscience ensures these requirements are met efficiently and in full compliance with applicable standards.
Network
In today’s highly specialized environment, the pitfalls lie deep in the details. That is why collaboration and networking are essential to our work. By engaging actively in professional associations, we ensure access to shared expertise, perspectives, and solutions- benefiting both our clients and our partners.
BVMA - Federal Association of Medical Contracting Organizations
The BVMA (Bundesverband Medizinischer Auftragsinstitute e.V.), founded in July 1991 and based in Munich, is the central interest group for German-speaking CROs (Contract Research Organizations). The association currently has around 51 member companies with a total of around 8,000 employees, representing over 80% of the German CRO market.
Since 2021, we have been an active member of the BVMA, strengthening our network and contributing to the advancement of industry standards.
SCDM - Society for Clinical Data Management
Founded in 1994, the Society for Clinical Data Management (SCDM) is a leading global non-profit professional society with over 3,000 members from more than 49 countries. Its goal is the professional development of clinical data science and the assurance of high-quality study data.
By partnering with the Society for Clinical Data Management (SCDM), we demonstrate our dedication to high-quality data management, consistent processes, and ongoing training. As active members of this global network, our employees gain advanced certifications and bring internationally recognized best practices straight into your study projects.
Biocom California
With over 30 years of experience, Biocom California is the leading life science organization in California. Since 1995, it has represented more than 750 member companies – including biotech, pharma, medtech and diagnostics companies – as well as universities, CROs and investors.
Being a member of Biocom California for many years strengthens Mediconomics’ position as a global life science service provider – in regulatory, commercial and network terms. It underscores our commitment to innovation, growth and partnership for the benefit of our clients.
European Medical Writers Association
The European Medical Writers Association (EMWA), founded in 1992, is one of the largest and most renowned European professional associations for medical communication and medical writing. As a non-profit organization by and for professionals from the pharmaceutical, research, medtech and academic worlds, it unites over 1,000 members from around 39 countries.
For over 20 years, we have been proud members of EMWA, the European Medical Writers Association. This underlines our dedication to clear, high-quality communication—delivering study documents that are not only scientifically sound but also maximize regulatory impact.
FAH - Research Association of Pharmaceutical Manufacturers
The FAH is a cross-industry association of German pharmaceutical manufacturers that promotes the exchange between industry, research and authorities. It supports its members with expertise on regulatory requirements, clinical research and drug safety.
Mediconomics benefits from up-to-date know-how on regulatory developments, a strong network and direct dialog with decision-makers in the pharmaceutical industry. In this way, we guarantee sound advice and tailor-made support for your projects.
ICR - The Institute of Clinical Research
The Institute of Clinical Research (ICR) is an independent, member-supported association for clinical research professionals. For over 50 years, the ICR has provided high quality training, networking opportunities and support to the clinical research community, both commercial and non-commercial.
As an ICR member, Mediconomics gains access to up-to-date specialist knowledge, practical training (e.g. GCP, monitoring), influence on regulatory developments. Membership also provides a strong professional network within the field of clinical research.
Partner
MLM Medical Labs
MLM Medical Labs is a leading international central laboratory with sites in Germany and the USA. The company offers a wide range of customized and fully integrated services specifically for clinical trials to support biopharmaceutical projects. MLM provides central laboratory services for clinical trials from a single source: from kit provision to fully automated diagnostic processes, special tests, sample logistics, strict quality assurance and regulatory-compliant data transmission.
Through our long-standing co-operation with MLM, we work hand-in-hand to support joint clients – ensuring efficient processing and optimum results.
Videoc Technologies AB
Viedoc is a user-friendly, web-based platform for Electronic Data Capture (EDC) in clinical trials. It enables efficient data capture, validation and management – ideal for studies of any complexity and phase.
Since 2019, Mediconomics has partnered with Viedoc to implement a modern, scalable and user-friendly EDC solution. This platform enables clinical trials to be conducted efficiently and in compliance with regulations, guaranteeing our customers high data quality, transparency and compliance in all phases of their studies.
