Existing Partners 2

Global Clinical Trials (GCT) is a full-service premium Contract Research Organization (CRO) supporting Phase I-IV clinical, medical device studies and post-marketing activities for Big Pharma, small and medium-sized biotech enterprises, groups and funds, as well as large universities and institutions.

Poseidon CRO has a unique in class geographical coverage including North Africa, Western Balkans and Hungary. We have an extensive network of collaborating sites and maintain a solid relationships with Key Opinion Leaders in all our regions. This is allowing us to perform all kinds of clinical trials, health market research studies, Outcome Research, patient support programs and pharmacoeconomics.
Our comitted team has a strong knowledge in regulatory processes and clinical operations and is used to manage efficiently the most complex and demanding trials, thanks to a continuous improvement policy, embedded since the start in the companie’s culture. We gained experience in various therapeutic areas such as oncology, diabetes and metabolic diseases, cardiology, respiratory, central nervous system, infectious diseases, ophthalmology, gastroenterology and gynaecology.

Our team is also providing medical translation of content allthrough the drug/medical device life cycle in English, French, Serbian, Arabic and Hungarian.

Founded in Ankara in 2016, MyCRO’s mission is to provide the highest quality at every stage of clinical research. We are bringing to you our 8 years of clinical research logistics support, and 10 years of experience in Clinical Research management in phase III and IV, Observational studies and medical device studies.

We are aware of the great potential of Turkey in clinical research, and with our past experiences, we are committed to high standards of quality and customer satisfaction in the future.

Klinar CRO was established as an Optimum CRO enterprise for the international trials conducted in Turkey. Both companies are conducting clinical trials since September 2000 in Turkey.
Our companies has a deep experience over the clinical trials of different phases and types and post-marketing surveillance studies.
With our extensive background in this field, our specialized team and with the philosophy of continuous improvement, we are ensuring to provide the services you need with the excellent process.

Klinar CRO has become one of the first certified CRO to be approved by the Ministry of Health in Turkey, working in compliance with the principles of “Guideline For Good Clinical Practices”.

Zi- Diligence is a leading biocenter in Egypt and the Middle East. Our Company offers a variety of services including Bioequivalence studies, Biowaver studies, and other pharmaceutical research services.

1st GCC accredited Biocenter in Egypt and 36th worldwide in addition to ISO 9001 & ISO 17025 certificates.

All studies are conducted under strict adherence to GCP & GLP principles in accordance with EMEA, FDA, ICH and WHO, with controlled calibrated equipments.

Gaea was established in 1994 as a clinical consultancy committed assist in the development of clinical development plans, and project management within sponsors.

Gaea is now a full-service agile CRO, working in complex indications and IMPs, where experience matters, serving all of Europe.

Gaea is also a trial acceleration company, to get slow trial sites moving in screening and enrolment leaving the CRO to manage the data.

IRIS CRO is Clinical Research Company established by experts, high level professionals in clinical research with more than 10 year experience in General Medicine, Oncology, one year experience in Cosmetics and Medical Device projects.

AquaClinical is a boutique Clinical Research Organisation specialising in Study Start-Up activities and ethical submissions. We manage the process from site feasibility through to Clinical Monitoring and Close-Out Visits.

Allied Clinical Management GmbH, founded in 2004, is a Berlin based CRO. We collaborate with large and small pharmaceutical and medical device sponsors. Our clinical research experts manage drug, medical device and ATMP trials in all phases according to ICH E6 (R3), CTR EU No. 536/2014, EN ISO 14155 and MDR regulations and guidelines. Our geographical coverage for clinical site management is Germany, Austria and Switzerland.
Our clients include international pharmaceutical companies, medical device manufacturers, biotechnology start-ups and academic investigators.
In addition, we provide functional services and supply CRAs, trial managers and other clinical operations professionals who work on a contract basis for our clients.

CONVIDIA clinical research GmbH combines exceptional experience with engagement.

CONVIDIA clinical research GmbH is an employee-owned company, consisting of 12 employees. Due to this setting our team’s engagement and identification with each project is maximized. Moreover, not to be forgotten established well-structured processes and quality standards.

The team currently and a pool of experienced freelancers.

We have worked for a whole range of sponsors: from mid-size companies in Germany and Europe, non-commercial institutions such as clinics and foundations that conduct investigator-initiated trials (IIT) to large globally acting pharmaceutical companies. Our team is hence familiar with different company cultures, including the complex structures and processes of global players.