IT project database
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 4622 IT projects that we have successfully completed with our customers.
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 …
Documentation and application of usability engineering to the concept and development of medical lab software according to international standard IEC 62366-1 and FDA law for medical devices. …
The customer is attempting to renew product approval (EU) for an electrically operated breast pump. The existing documentation and records do not meet the current regulatory requirements in terms of structure, content …
Creation and documentation of test cases for a warehouse management system adapted to a specific customer; undertaking the SAT (system acceptance test) and deriving defects. …
The aim of the project is to supervise various usability activities in the upgrade to a new version of an existing product. One important factor here is documentation, which is used as …
The customer manufactures a pooling instrument for the international market that needs to fulfill FDA requirements. PTA supports the customer in the field of software development in formulating the requirements, and revising …
All regulatory requirements regarding creation and documentation of test scripts for warehouse management system that has been adapted based on customer-specific changes. …
Creating, checking and performing test cases in a pharmaceutical laboratory project. Performing manual tests of the tool in laboratory conditions according to FDA guidelines. Check of sufficient and correct usage of existing …
Software is further developed for a tool that has been on the market for several years. A subproject of this update is to reflect existing requirements and their traceability in compliance with …
A laboratory middleware is to be further developed and a customer-specific graphic design framework to be modified on the basis of an existing application. For this purpose, the project team will rework …
An existing software solution for POCT (point-of-care testing) devices is to be enhanced for the American market and the associated regulatory requirements. …
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 MES system (Manufacturing Execution System) for galenic development enables GMP-compliant documentation of developmental and clinical sample approaches in the development department for parenterals (medication that is administered without passing through the …
Consultancy services in a project for migrating packaging specifications from the QM module in SAP R/3 to a document management system with an interface to mySAP.com. …
Support, maintenance and further development of an inventory management system with interfaces to SAP R/2 and R/3. …
The validated test database system is used to map project- and process-oriented general (not merely software) test cases and test sequences, to manage the results of these tests and to create the …
Leading project supervision on the part of SAP first level support. As part of this project, a system is developed that is able to map packaging specifications while fulfilling the GMP requirements …
Involvement in introducing mySAP ERP 2004. The standard software is introduced for three production sites (one in Austria and two in Switzerland); all three companies already use an in-house SAP R/3 system, …
Revision of an IT consultancy's project handbook based on the requirements of the FDA for the development of IT systems as defined in the "General principles of software validation" …
Assistance of an IT consultancy company during an audit by an international pharmaceutical group. The audit is to examine the degree of compliance with the requirements for IT systems issued by the …
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 …
Further development and rollout of the authorization concept in an SAP system landscape, which includes R/3 systems, HR, BW and SEM systems. …
Preparation and documentation for a complex system replacement of the MES individual software with the PMX standard software. …
Development of a new application for mapping, managing and maintaining launch plans for new products. The application is validated and further developed in line with FDA guidelines. An electronic signature for product …
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