Mediconomics GmbH is a full-service CRO headquartered in Hannover, Germany, with subsidiaries and affiliated companies located in the UK, Denmark, Switzerland, and the US.
We are experts in consultancy and new regulatory requirements; with a successful
track record of almost 20 years supporting pharmaceutical, biotech, and medical
device companies, in all phases of clinical development.
As an international service organisation, we recognise the role that our representatives play in building strong customer relationships. They represent a consummate balance of science and business; allowing us to achieve clinical excellence, technological innovation, and bottom-line productivity, whilst maintaining the highest quality standards. A flat hierarchy enables rapid and informed decision-making in response to our client’s requests and requirements.
Solutions are tailor-made for clients and additional marketing opportunities are contributed via our sister company: Medicoforum GmbH. Successful task completion credits our high client satisfaction rating, encouraging repeat business and promoting new business for the future.
DRK Pharma Solutions is a leading clinical research organization providing Phase II – Phase IV clinical trial management in Asia through highly experienced professionals & world-class infrastructure. The team has conducted over 70 multinational and multi-center Phase II –IV clinical trials in various therapeutic segments.
Our regional site Pakistan having the world’s 6th largest population (220 million), treatment naïve patients and encouraging regulatory framework (Regulatory approvals in 4 - 5 months) is an ideal market for conducting clinical trials. Pakistan also has the advantage of not having many competing trials & unburdened sites allowing quick patient recruitment. Pakistan has the largest breast cancer burden along with one of the highest ratio of Cardiovascular, Diabetes, Hypertension, Rare Diseases and Cancer affected population in the world. We have ICH/GCP trained site staff, foreign qualified PIs in the region.
Numerous multinational pharmaceutical companies have conducted clinical trials in Pakistan contributing successfully in providing clinical trials data for drugs registrations with US FDA, EMA, etc.
Aixial is the CRO of ALTEN Group (www.alten.com), a large and profitable group with revenues in 2017 of 2 Billions € and 28 000 people worldwide.
Aixial is a full-services CRO with 4 main fields of expertise: Clinical Operations, Clinical Data Science, Vigilance, Regulatory Affairs.
Aixial’s strategy is to develop the long-term partnerships with its clients thanks to its quality of theservices and of its people and to be the alternative between Global CROs and Local CROs.
Some of the countries we provide the full clinical support are: France, Belgium, Switzerland, Germany, the Czech Republic, Slovakia.
Our clients deserve to work with the best talents with the best proactivity and reactivity, flexibility and transparence.
With 500 people in July 2018 and revenues of about 40M € in 2017, AIXIAL is among the Top 5 European CROs.
As a local contract research organization, we conduct multicenter and single center clinical studies within Bulgaria.
Our capabilities cover A – Z clinical research services starting from: feasibility assessment, study teams and sites selection, budget management, contracts negotiation, medical writing, regulatory activities, investigator meeting organization, study start-up support, study team training, project management, subjects recruitment, sites management, vendors management, clinical monitoring, safety reporting, auditing, data management, biostatistics, final report development and scientific consulting.
On the other hand, our privately-owned center for early phase human and drug research with a built-in phase I unit enables us to conduct a variety of single-center clinical research on healthy volunteers and specific patient populations:
Marti Farm Ltd., company based in Zagreb, Croatia is a contract research organization supporting the needs of the companies working within pharmaceuticals, biotechnology, medical devices, food supplements, cosmetics and healthcare industries across a variety of consulting and operational services.
Mart Farm Ltd.provides the following services:
We are internationally recognized as a reliable partner and provider of consultancy and regulatory services with a proven track record of 9+ years. Our core belief is continuous personal development aimed at strengthening our expertise and approaches in order to drive added value for our clients from both the operational and the strategic aspects.
Over the last several years, we have been increasingly expanding our business internationally in search for new satisfied clients and trusted partners.
Being a leading contract research organization (CRO) in Taiwan, Bestat is dedicated to offer clinical services with the highest quality.
As experienced professionals within the industry, we provide customized services, which can be deployed on a stand-alone basis or as part of an integrated “comprehensive-service” solution, including:
Our teams always have the good professional spirit with highly efficiency and cooperated attitude. You can trust that we will be your good partner. So we are the best choice for you. Welcome to contact us if you are interested in Bestat.
JMedTec is an elite service provider headquartered in China for regulatory affairs and clinical trials for both pharmaceuticals and medical devices.
We provide full services for product market entry in China/Asia with four fields of expertise: regulatory affairs, clinical operations, vigilance and local distribution management.
Our professionals all had senior working roles in global manufacturers and provide practical know-how for the local market to help the international clients to overcome the market entry barrier in China/Asia.
Brillance is independent, Polish CRO specialized in monitoring and management of phase I-IV clinical trials (medical products and devices) in Poland, Czech Republic and Slovakia. Since 2004 offers services both for local and local parts of global projects for pharmaceutical, biotech or other CRO companies. Regionally operating offers a deep insight into local markets thanks to excellent relationships with sites, staff and knowledge of local authorities requirements. Brillance deals with trials in almost all therapeutic areas, most currently in (hemato)oncology and cardiology. It is well known for flexibility, patients quick recruitment and delivering quality data. Professional regulatory team handles challenging cases and its lawyers cover demanding sites/investigators contracting. US Clients with no presence in EU are guided and represented by Brillance locally.
SMO-Pharmina is providing superior clinical trial management services in Georgia: ensuring quality care for patients, adherence to international guidelines and delivery of reliable data.
Since 2006, LTD SMO-Pharmina has contributed to the establishment of GCP compliant clinics. Nowadays, the company has set up the renewable database of clinical trial sites and Principal Investigators in all therapeutic areas. SMO-Pharmina has worked with up to 100 clients as SMO or CRO. Over 100 sites managed by SMO-Pharmina have undergone about 140 successful audits and 2 FDA inspections.
SMO-Pharmina ensures effective management of the entire project from start-up to close-out and offers the clients the following services: Site Selection, Project Management, Regulatory Affairs, Site Monitoring, Study Coordinator support, Training Center, Clinical Laboratory, Pharmaceutical Warehouse, Archive, Distribution of clinical trial materials, Logistic support.
AnRes Clinical is a small CRO/consultancy, composed of a small team of passionate clinical Project Managers, Clinical Research Associates, Regulatory Submission specialists, Site Contract Managers, Medical Consultants, Statisticians, PV Experts and Regulatory Affairs professionals with a wealth of experience. We mainly work on a freelance basis. In addition to that we partnered with a clinical database development partner who can create eCRFs, eQuestionnaires, ePatient Daries, ePROs and many other databases tailored to study needs. Our current global reach includes Scandinavia, Europe and United States. What makes us different is passion, wealth of experience and collaborative approach. We specialise in running clinical trials in Rare diseases, Oncology, Neurology and Cardiology medical devices, however we also work in a number of other therapeutic indications. Our mission is to partner with biopharmaceutical companies and Clinical Research Organisations in order to support development of better medicines.
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