Auditing

VEQTOR helps you prepare for a successful regulatory inspection or standard bodies certification. Certainly, preparation for regulatory inspections or a standard bodies certification is challenging for any company, no matter how large or small. The VEQTOR team has extensive and specialized experience in successfully helping businesses prepare for every challenge associated with regulatory inspection and certification bodies readiness. Our Quality Assurance Specialists and Compliance Team thoroughly review all existing quality management systems to ensure that they meet regulatory requirements and provide affordable and convenient one-stop customized solutions. Auditing doesn’t have to be a costly and complex burden that’s put off until mandated. Our affordable, custom, end-to-end solutions help proactively implement critical solutions.

VEQTOR’s Services & Support Include:

  • Internal Auditing
  • Supplier Audits and Planning
  • Vendor Agreements
  • cGMP Readiness
  • ISO 9001:2015 and ISO 13485 Readiness
  • Gap Assessment Against the Entity Requirements
  • Revision and Preparation of all Relevant Documents
  • Regulatory Inspection Readiness and Mock Audit focused on but not limited to FDA, EMEA, MHRA, and Health Canada
  • The development and conduct of cGxP training programs for Biopharmaceutical, Medical Devices, Pharmaceutical, and Cosmetics organizations.
  • Audit Response and Remediation Development
  • Robust Audit Training Programs focused on your organization

Learn more about our value-driven personalized services for the Life Science Industry.

Contact VEQTOR