In order to help businesses meet the dynamics and challenges of evolving global regulatory compliance standards, Connvertex Technologies provides expert solutions for efficient reporting, submission and validation of regulatory data. By exercising company-wide regulatory capabilities, our experts help businesses seamlessly and effectively handle, track and manage submission costs through services including:
- Computer Systems Validation, CAPA – Given the standard rule for manufacturers of biological, pharmaceutical and medical devices to have a Corrective and Prevention Action (CAPA) procedure in use, Connvertex assists businesses with regular CAPA audits for identifying loopholes & backlogs in CAPA system. This helps businesses comply with regulatory obligations while preventing new issues from arising.
- Implementation and Validation Services – In order to help businesses perform in sync with Good Manufacturing Practices (GMP), we provide expert assistance for implementation & validation of plans, to ensure that your system performs exactly as it is designed to.
- Regulatory Based Submissions – In compliance with the performance standards of U.S. Food & Drug Administration (FDA), Connvertex assists businesses with regulated product submissions.
- Good Practice (GxP) Guidelines – Given the significance of quality in industries like Pharmaceutical, Medical Devices, Biotech, etc., Connvertex ensures that companies abide by good practice guidelines and the products meet their intended use, quality and safety standards.