CRO – Contract Research Organisation
CRO- Institut für klinische Forschung - Dr. Oestreich + Partner GmbH
In its capacity as a CRO (Contract Research Organisation) the company Dr. Oestreich + Partner GmbH, provides budget, time and goal-oriented consultancy and support for clinical studies. The spectrum of services provided ranges from the initial budget planning through to successful conduct and reporting of clinical trials in the prevention, treatment, care and economics of diverse medical indications. Our broad network of local clinical monitors and partners with ICH-GCP experience enables flexible implementation of our CRO – Contract Research Organisation - services in a very broad range of clinical studies at home and abroad.
The CRO (Contrat Research Organisation), which was founded in 1991, has extensive experience in clinical research. Our highly qualified and extremely competent team supports our customers with a comprehensive range of services. We carry out national and international clinical research projects for the prevention, treatment, care and economics of all medical conditions and issues.
CRO - Contract Research Organisation - Individual Solutions for Greater Flexibility
As a CRO (Contract Research Organisation), our areas of responsibility include the preparation of all the necessary documents - from regulatory submissions to the authorities and protocol development for clinical trials in prophylaxis, therapy, supply and economics of all medical indications and issues; the drafting of investigator contracts through to the writing of publications. As a CRO (Contract Research Organisation) we are very happy to additionally carry out comprehensive literature reviews and the translation of texts and documentation. We design, draft and create case report forms (CRFs) according to the different trial endpoints. Our Electronic Data Capture (EDC) systems OPVERDI and PMSBOX additionally allow the individual creation of multilingual fast online eCRFs. At the same time, those with authorised access to these data bases may access all relevant data in real time, which enables project participants to organise their work in an extremely flexible manner.
We monitor clinical trials from Phase I to IV, and recruit and instruct trial sites and laboratories. In addition, we conduct both the on-site and online monitoring of clinical trials, and carry out audits and implement other quality assurance measures. At the same time, the CRO’s (Contract Research Organisation’s) project management personnel closely track the project budget and accounting, while all the time ensuring careful and rigorous pursuit of our clients’ objectives.
A detailed overview of our Contract Rsearch Organisation (CRO) is found here: