Clinical Investigators

Efficient and reliable software solutions for Clinical Investigators

In the conduct of clinical studies in the prevention, treatment, care and economics in all medical indications, Dr. Oestreich + Partner GmbH provides investigators with efficient and reliable EDC software solutions for data management and budgeting.

By means of different content management and documentation systems, we can provide investigators with a structured patient-selection process for time- and goal-oriented recruitment and as a controlled basis for fast and optimal study start. Our online Electronic Data Capture (EDC) systems OPVERDI and PMSBOX are used to create individual and multilingual eCRFs and to integrate separate investigation results such as ECG, ultrasound, laboratory findings or telemedicine self-monitoring of patients. For investigators and other authorised persons, all the data in the study centre is available up-to-date and in real time without having to be present at the study site. This enables a flexible and demand-driven task organisation, which is optimised with respect to costs.

Clinical Investigators - linear data by patient self-monitoring

During the clinical study, we provide telemedicine measuring devices for patient self-monitoring with easy-to-use devices, wireless transmission technology plus the function to store and process the information on powerful computer networks. Vital parameters such as ECG, heart rate, blood pressure, oxygen saturation, body weight, body temperature, respiration, blood sugar, and so forth, can be measured at any time by both stationary and ambulant patients. This telemedicine self-monitoring of patients provides investigators with accurate, current data online without study site visits being necessary.

As a full-service clinical research company, we are pleased to provide translations of all medical texts - from the study plan through to the preparation of CRFs, templates for investigator contracts, records for doctors, publications, and so forth. We will also gladly carry out an extensive literature search for project-related subjects.

With regard to the increasing demands through more and more regulations, laws and guidelines, we offer information evenings, seminars and practical training in our training centre in Cologne. These include, for example, practical training sessions for investigators and study assistants on "Good Clinical Practice (GCP) or “Standardising and compliance with SOPs - planning through to evaluation.”

Detailed information on clinical research for investigators can be found here:

http://www.oandp-cro.com/clinical-research/product-safety/


EMEA Pharmacovigilance
Health care studies
Observational studies
EMA Pharmacovigilance
Medical Biometrics
Approval of Medical Devices
Pharmacovigilance
Clinical Investigators
Clinical Trials
GCP Legislation
GCP - Good Clinical Practice
ICH GCP E6
GCP Guidelines
GCP Compliance
BfArM GCP
CRO – Clinical Research Organisation
CRO – Contract Research Organisation
PSUR
PSURs
Pharmacoeconomics, Health
Pharmacoeconomic studies
Pharmacoeconomics
Patient Monitoring
Monitoring Clinical Trials
Clinical Monitor
Marketing Authorisation
Medicinal Product Approval
Drug safety
Data management plan
Clinical development
Monitoring investigators
Non-interventional studies (NIS)
Patient recruitment
Phase IV studies
Investigator audit
Investigator qualification
Investigator selection

EMEA Pharmacovigilance · Health care studies · Observational studies · EMA Pharmacovigilance · Medical Biometrics · Approval of Medical Devices · Pharmacovigilance · Clinical Investigators · Clinical Trials · GCP Legislation · GCP - Good Clinical Practice · ICH GCP E6 · GCP Guidelines · GCP Compliance · BfArM GCP · CRO – Clinical Research Organisation · CRO – Contract Research Organisation · PSUR · PSURs · Pharmacoeconomics, Health · Pharmacoeconomic studies · Pharmacoeconomics · Patient Monitoring · Monitoring Clinical Trials · Clinical Monitor · Marketing Authorisation · Medicinal Product Approval · Drug safety · Data management plan · Clinical development · Monitoring investigators · Non-interventional studies (NIS) · Patient recruitment · Phase IV studies · Investigator audit · Investigator qualification · Investigator selection