Auditing

For more than a decade PathWise has provided its clients with the skills and tools necessary to manage quality system regulations, including conducting investigations.

Much of our time is spent performing third party audits for company improvement efforts, supplier determination, or FDA prep inspections, whatever the cause we have a number of industry experts available as a resource to your organization.

Additionally, we have a training course geared toward internal, external, and supplier auditors to better understand pertinent regulatory requirements, guidelines, standards, scheduling, planning, performing the audit, and writing the audit report.

In this day and age when suppliers and manufactures are sometimes half a world away, having a third party resource to perform audits or to prepare your people to perform the audits is essential.

PathWise not only provides an outside perspective to these issues, we bring proven best-practices, tools, and processes. We’ve studied the best of the best in the life sciences field, and bring an intimate knowledge of the FDA regulation and ISO requirements.

Learn more about our solutions for Medical Device or Pharmaceutical companies.

Pharmaceutical

Developing a systematic approach to cGMP compliance isn’t easy. PathWise provides tools, systems, and best practices to simplify regulatory compliance for Pharmaceutical companies.

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Medical Devices

The Quality System, QSR, presents a layer of complexity for many Medical Device companies. PathWise has the experience in helping to manage your quality systems that meet the challenges of regulatory compliance for Medical Device companies.

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Pathwise Solutions

Through training in PathWise Project Success managers learned a process for the selection and approval of projects. Team leaders and team members acquired the skills to accomplish projects on time and within scope.

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