The arivis5D cloud platform can be considered as a collection of cloud services connected by APIs. You build up from processes and their data to the functional services and then combine those services into composite applications. Such arivis5D applications as arivis5D Compliance, arivis5D Protocol, arivis5D Information and arivis5D Raw Data represent various phases in the life sciences life cycle.
This approach is the service-based or service-oriented architecture, at its essence. With this change in paradigm – away from tightly coupled applications that focus on the user interface – arivis5D as a platform rather exposes the underlying business functions as connected services which can leverage complexity in nearly every process landscape in the life science industry.
Our applications span the entire lifecycle through drug discovery, development towards market access and continuously leverage innovation
arivis is a market leading software company focused on the life sciences industry. With a broad product portfolio and subject matter expertise, our solutions address industry and academic intelligent information and imaging needs. Our products are innovative, scalable, award-winning and based on state-of-the art technologies
Functional areas can be arranged as a hierarchy of processes, so that certain areas can be broken into interacting sub-processes. An efficient process landscape directly adds value to an organization.
Auditing is a vital function within a pharmaceutical company nowadays. Quality audit is a review and evaluation of all or part of a quality system with the specific purpose of improving it. A quality audit is usually conducted by external or independent experts or by a team designated by management for this purpose. These audits can be extended to suppliers and contractors as well. An audit will assess the strengths and weaknesses of quality assurance and quality assurance processes.
Auditing is a basic capacity inside a pharmaceutical organization. It furnishes the board with data about how adequately the organization controls the quality of their procedures and items. Auditors must play out their occupations capability to guarantee their organization's consistence with pharmaceutical USFDA GMP guidelines and other quality standard like ICH Q10.