We are a full-service clinical research organization with over 30 years of experience in clinical trials
AtoZ CRO initiates, plans and monitors clinical studies of pharmaceuticals, therapeutics and medical products for national and international clients. In over 30 years we have gathered experience in all important areas of therapeutics. The countries of Eastern Europe have been a geographical focal area from the beginning in 1984. By now, we have extended our services worldwide and are also offering animal studies.
Our team consists of 15 highly dedicated and motivated people with vast experience in clinical studies and diverse backgrounds ranging from medical experts, pharmacists, life scientists, biologists and nutrionists. We support you from the initial planning stage including the preparation of study protocols to regulatory affairs and legal submissions. Furthermore, our services encompass:
Planning and initiation of clinical studies
From its head office in Overath, Germany, AtoZ-CRO manages and coordinates clinical studies of phase 0 to IV and post-marketing studies for national and international clients all over the world. We accompany your study from the first step until the final report – this includes the preparation of the study protocol and synopsis as well as potential changes, always in accordance with your guidelines.
The AtoZ-CRO is not only a specialist in planning but also in conducting clinical studies. Amongst others we offer the recruitment and assessment of study centers, the training of investigators and their staff and monitoring the study centers incl. source data check.
Design and implementation of CRFs (case report forms) and eCRFs
With our team of experts we can offer you the right CRF, may it be electronical or not, suitable for your study and according to your specific study needs.
Biometry and statistics
To successfully complete a study, AtoZ-CRO offers its Biometry and Statistics services through a long lasting and reliable partner. Amongst others, data collation, validation, analysis and report, including sequential collation and analysis are the main activities.
Regulatory affairs issues
The AtoZ team is not only experienced in planning your study but also an essential partner when it comes to submit your study. Trust our more than 30 years’ of experience!
Medical, clinical and safety regulatory affairs in the EU and a 24-hour physician stand-by service is included as well. Two AtoZ’ employees are certified and empowered to take care of any issue regarding the Pharmacovigilance such as LQPPV and local literature screening.
A history worth mentioning
Years of Experience
Get in touch
If you want to inquire about our services or have any questions please contact us directly at email@example.com or +49 2206 95 99 0 or you can use the field below.