EMEA Pharmacovigilance
EMEA Pharmacovigilance
The fulfilment of the requirements and conditions of the EMEA data-processing network and pharmacovigilance database EudraVigilance and the implementation of an action plan for risk management in line with the EU pharmacovigilance directives are of the highest priority at Dr. Oestreich Partner GmbH together with strict orientation to the customer’s specific requirements. For well over two decades the Company has conducted pharmacovigilance projects in various medical indications and specialist areas in accordance with the EMEA guidelines. Our SOPs reflect the current EMEA pharmacovigilance guidance as the standard for our internal work processes. Our expert and highly qualified team has extensive experience in both the medical and requisite technical areas, and is available to assist our customers in EMEA-driven pharmacovigilance projects. The identification, documentation, reporting, monitoring and evaluation of events with respect to the safety and tolerability of pharmaceuticals and medical products are all carried out in accordance with the EMEA pharmacovigilance requirements. We plan both retrospective and prospective studies to establish any interrelationships between different medicinal products (drug interactions), misuse and other safety profiles. These projects are carried out with careful consideration of the cost-benefit analyses. We also manage the reporting of adverse events to the competent authorities, and the associated long-term monitoring and data management for our customers. In addition, we prepare safety update reports (PSURs) for authorities, analyse medical texts and other sources on medical product safety and summarise study results according to EMEA pharmacovigilance requirements.
Click here for an overview on EMEA pharmacovigilance:
http://www.oandp-cro.com/clinical-research/product-safety/
Fast transmission of pharmacovigilance data to the EMEA
With our internet-based EDC programmes OPVERDI and PMSBOX, we provide our customers with practice-oriented databases, which can be adapted, both in their design and data structure, to the individual needs of all EMEA pharmacovigilance studies. Access to our databases is possible via the internet, which means that the systems have high intrinsic flexibility with all authorised users able to view or edit data from any location. These software solutions, which meet regulatory authority requirements, have been in use for more than 10 years. In addition to high reliability, inbuilt error prevention checks and uncomplicated data correction, they permit rapid communication while at the same time ensuring data security for the protection of patients. The databases also enable the easy transmission of data to the EMEA (EudraVigilance data processing network and management system) or other EMEA pharmacovigilance data collection systems.
Click here for more information on EMEA pharmacovigilance:
