Vieco Pharmaceuticals Goes Live with AmpleLogic DMS and QMS System

Vieco Pharmaceuticals Goes Live with AmpleLogic DMS and QMS System

AmpleLogic is delighted to announce the successful implementation of Document Management System (DMS) and Quality Management Software (QMS) at Vieco Pharmaceuticals, Dubai.

We would like to take the opportunity to thank everyone involved in this implementation for their support, enthusiasm, and hard work during the course of this project.

AmpleLogic web-based Electronic QMS System which enables them to manage, monitor and control the required quality processes. This Electronic EQMS Software will also streamline the process of meeting regulatory compliance standards and in ensuring data integrity. Our QMS Software modules increase accuracy, increase productivity, efficiency and provide consistency across functional departments and processes by ensuring that everyone is using the same data.

The DMS System provides a centralized system for storing all controlled documents, as well as any revisions for access and archiving, etc. This Document Management Module also provides the ability to establish automated document review, approvals, as well as controlling restricted and unrestricted documents based on type. With AmpleLogic Electronic Document Management System (DMS) Software organizations can create and control policies, Work Instructions, Standard Operating Procedures (SOPs), Manual and reports dynamically, in compliance with regulatory standards. 

Our GMP Software Solutions is purpose-built for the life sciences sector, and eases the burden of managing quality processes, as well as solving non-quality related issues within your company and all solutions are compliant with FDA, WHO, EU Annex 11, cGMP, MHRA, ISO, and other regulations and standards that apply to their drug products.

Learn more about how the AmpleLogic Quality Assurance Solutions module supports the entire quality management and document management processes

About Vieco Pharmaceuticals

Vieco Pharmaceuticals was founded in 2014 in response to the tremendous market need for high-quality medicines in the region, as well as for the need for the latest pharmaceutical production technologies while complying with the latest international standard – Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP) and Good Distribution Practices (GDP). In that sense, Vieco will play an important role in improving the quality of local healthcare.

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