Are your Clinical Records in compliance with these government Requirements?
- 21 CFR Parts 312 and 314
- ICH E6 Guideline for Good Clinical Practice
- CPGM 7348.810
In the Biotech, Regenerative Medicine, and Pharmaceutical industries, Records Management demands are escalating as both paper and electronic copies easily overwhelms a company's ability to store, track, and retrieve a document at a moments notice. Furthermore, Records Management has precise FDA requirements. Detailed knowledge of these FDA requirements and its frequent updates requires a certain level of knowledge and expertise. This knowledge and expertise is critical for your company to remain in compliance. WaveFront ensures that your company's files meet industry regulations.
- Clinical and Regulatory Records Management
- Documentation Workflow Solutions
- Document Archiving Solutions
WaveFront is not a recruiting agency that sends consultants to your companythat you then hire and manage.
WaveFront provides a service that sends its own employees to your company.
WaveFront is responsible for its employee's management, benefits, and payroll.
We pass the cost savings on to you!
Document Workflow Solutions
Document Archiving Solutions
Document Imaging Solutions
Document Room Design
Pre-Audit Compliance Checkups
WaveFront provides complete Records Management services designed to fit your company's requirements and budgets by equipping you with the resources and expertise to manage your files whether your company is small or large. If you are looking for an electronic document solution or file room solution, our highly trained staff can design and implement a complete filing process, or upgrade and/or maintain an existing filing process. WaveFront can work with your files at your location and our services can be tailored to meet your company's specific needs.
Are Your Clinical Records Out of Control?
Are They In Compliance?
UNSURE? - CONTACT US