We evaluate the risk of side effects potentially associated with the new products.
We provide Medical Writing services to produce a clear and complete documentation.
We offer a complete service to manage correctly the clinical Documentation.
We manage either electronic data and paper based information.
Last generation IVRS (Interactive Voice Response System) technology.
We provide a quality assurance service during all the phases of clinical development.
We assign to each medical research a specialized team of Project Managers.
We manage integrated statistical analysis plans for companies and institutes.
OPIS is an international company providing services to pharmaceutical, biotechnological and medical industries. Our portfolio includes the development and management of programs in support of the clinical trials, from the launch phase to the use of data, and we coordinate the results distribution activities.
The OPIS eCRF (Clinical.NET) is a web-based system fully developed and managed by the Clinical ITC department. The system architecture is based on a Three-Tier model. The system has been validated in accordance with the regulatory requirements of 21 CFR Part 11, which regulates the characteristics of safety, traceability, availability and data integrity.
The team of OPIS Quality Assurance provides a quality assurance service to support the Client during all the phases of clinical development, putting the pre-clinical, clinical and technical expertise at the service of the research team, in order to achieve the highest standards.
OPIS is able to provide niche services to meet the needs of the Sponsor that does not always have the necessary experience and directly exercising its competence both in creating and developing a “turnkey” product, and proposing itself as a reliable partner.
Clinical Research Associate
• Scientifical Degree
• At least 1 year experience in Clinical Studies management
• Less than 30 years old
• Good knowledge of English language