IT project database
IT project database: The expert knowledge of our IT consultancy
Convince yourself of the range of our IT consulting services and our unique expertise, which we make transparent for you with our IT project database. With the help of filters and keyword searches, you can search through 4905 IT projects that we have successfully completed with our customers.
When using a LIMS for data collection in the routine operations of a biopharmaceutical manufacturer, incorrect data entries occur regularly. The errors are identified by analyzing the data in a data warehouse. …
The client, a pharmaceutical company, is introducing an ALM tool with the support of PTA. This tool is to support a number of processes in the future. Within the scope of the …
Our customer, a pharmaceutical company, would like to be advised and supported in all audit phases at two national companies and asks to document and complete all audit activities. …
To expand the market access for a successful LIMS, the manufacturer is requested to prove that the basic requirements of GxP guidelines can be fulfilled with the existing LIMS. Essentially, this means …
Quality assurance and approval of Potentially Reportable Incidents (PRIs) and Quarterly Complaint Check. …
The aim is to set up a quality management system (for Quality and Regulatory) and post audit support in the company's Middle East Management Center (MCME). …
Introduction of JIRA in order to maintain tasks for computer system validation (csv) with Scrum board for weekly sprint. Benefits: Validation activities become transparent for stakeholders. They become schedulable and evaluable. After …
The goal is to set up a quality management system (for quality and regulatory) in the Management Center Middle East (MCME) of the company and post audit support for Management Center Middle …
The aim of the project is to harmonise the business processes of the local subsidiaries of an international Diabetes care company and to support the countries in the implementation of these processes. …
The task of being responsible for quality is taken over on a mandate basis for a medical equipment manufacturer which develops, manufactures and sells infusion pumps (medical equipment class IIb). …
A medium-sized laboratory is supported by the documentation and validation of computer, measurement, and laboratory systems in accordance with the FDA/GxP standard, so that they can subsequently be audited. An action list …
Specification, programming and documentation of an inventory management for GxP-relevant assets and equipment and CSV-relevant (computerized system validation) documents and processes. …
The proper functioning of the inventory management in the standard SAP software is ensured in the validated environment by means of process and system tests. …
In the course of implementing the SAP standard software in a validated environment (GMP), a medical product manufacturer's business processes are harmonized with the business processes at an affiliate. Test management and …
The standard PMX-MES (Manufacturing Execution System) software is individually adjusted in accordance with the pharmaceutical company's requirements in order to fulfill certain guidelines (FDA, GMP) and to provide documentation in the form …
Creating, archiving and managing plans, logs and reports concerning all the production technology qualification activities. Creating monthly quality metrics reports for calibration and a three-monthly report for qualification. …
Creating and preparing GxP classification reports for production of parenterals as the basis for the process of validating production plants. …
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