A French SME offers clinical data management and drug safety/pharmacovigilance software solutions for human health and animal health under services or software licence agreements
A French company, specialized in clinical data management (CDM) and pharmacovigilance (PV) software solutions, is providing services including consulting, software development, validation (CSV - computerized system validation), technical and functional support, on-line and on-site training, data management and pharmacovigilance programming. They are looking for human or animal health partners for services or software licence agreements, to secure and optimize products' development.
The company is looking for partners who need to improve their clinical data management or pharmacovigilance activities via services or software licence agreements. The company is also looking for partners interested by license agreements to access the different software solutions proposed. Services agreement can be provided through up-to-date development and collaboration. Role / Task to be done : Partners will select the most appropriate software in close relationship with the company. Partners/End users will train the software in order to be able to use the app. Partners will contribute to the improvement and customisation modules.
Within the constant evolution of worldwide clinical trials and pharmacovigilance regulations and technology improvements, enterprises in the pharmaceutical and cosmetology industry see themselves strictly required to update their content and way of proceeding. Specialized in clinical data management and pharmacovigilance, the French company's experts are constantly updating their knowledge to propose the latest solutions in these fields, in order to improve performance, data quality, to assure and optimize products development in a secure way. The company is specialized in clinical data management and pharmacovigilance activities and proposes a wide range of services related to the utilization of software in this area. The company is supporting the customers at each step of the implementation of an application: selection of the most appropriate tool, validation of the application, improvement of processes, creation of process documentation, development of training modules, training of users, installation and support. In the data management (DM) field, the company's expert may perform study build and study programming. In data management and pharmacovigilance, the company can complete data analysis tasks. The company is also developing customized software to complete the performance of the existing applications. They are looking for human or animal health partners for services or licence agreements to access the different software solutions proposed.
Advantages and innovations
- Regulatory topics included always up-to-date - Data quality - of huge importance as data management, pharmacolvigilance and human or animal health are closely linked. - High level of performance - Gain of time in the implementation of the task and reports thanks to the software - Expertise and complementarity of the team of the consultants of the company including technical, functional and regulatory topics fiels to improve and have an up-to-date software. The company is operating internationally and is acknowledged by pharmaceutical companies, biotech and CROs (Contract Research Organizations) of various sizes. The company is already partner with several key operators of the pharmaceutical industry and may therefore propose a wide set of solutions.
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