Our quality team has been developing phase appropriate quality departments and programs for both clinical and commercial organizations. From the clinical side we often help with the creation of quality programs, managing external partners, development of quality systems, auditing and inspection readiness. On the commercial side we often help with remediation activities, tech transfer, harmonization, training, and continuous improvement programs.

Verity’s regulatory team has two primary focuses; submission and strategy. We understand the complexities of filing regulatory documentation and are here to ensure that your product is submitted properly. From INDs, to 510ks, to NDAs and beyond there is no filing too complex. From a strategic standpoint we are able to provide guidance and direction when dealing with external notified bodies, creating your regulatory plans, or commercial preparation for your organization.

Our primary validation focus is on computer systems. With the increasing demand for electronic systems and the pressure to remain compliant we have dedicated ourselves to becoming the experts. Our team helps from all aspects of planning, development, implementation, and go-live. We ensure your organization has the tools to successfully function in this connected world.