Support during COVID-19

Regulatory Consulting

AXSource has successfully supported importers/exporter, distributors, and manufacturers with small and large-scale regulatory projects for the past 30 years. To find out more about the COVID-19 regulatory pathways for products under the Health Canada Interim Order, contact us today.

Clinical Affairs

COVID-19 has impacted the way we conduct clinical trials. Whether you are at the application stage or currently conducting a clinical trial, AXSource can help. Contact us today to learn more about the new and creative ways to meet GCP compliance. For more information on our expertise and service offerings in clinical affairs, click here.

GMP Compliance

Regulatory agencies continue to perform inspections during COVID-19. Whether you would like more information on what to expect from agencies during COVID-19 or need support in meeting your firm’s compliance needs at this time, AXSource can help. Our highly qualified consultants have fully supported the compliance needs for hundreds of clients in North America, Europe, and Asia.

Computer System Validation

AXSource is the only Regulatory Affairs & Quality Assurance consulting firm with an in-depth background in Digital Transformation and Computer System Validation (CSV). As companies move towards a more remote setup during COVID-19, the need for validation of systems may arise. To learn more about the depth of validation expertise we can provide, please visit our page on Software & Systems Validation.