I offer specialized services to help your organization establish and maintain robust QMS frameworks. I provide tailored solutions for various standards, including ISO 9001, 14001, 17025, ISO 13485 (Medical Devices), and GMP (Good Manufacturing Practices), GCP (Good Clinical Practice), and GLP (Good Laboratory Practice).
My services include:
- QMS Creation and Implementation: Whether you're seeking compliance with ISO standards or GMP regulations, I will design and implement a comprehensive QMS suited to your organization’s needs. This includes creating SOPs, managing documentation systems, and developing CAPA procedures.
- Internal Audits: For clients in Ontario, I conduct internal audits to assess your current systems and identify areas for improvement. I ensure that your systems align with both ISO and GMP requirements, preparing you for external audits or certifications.
- Training Programs: I offer on-site and remote training programs for your team to ensure full understanding of GMP, ISO standards, and other regulatory guidelines. My goal is to empower your staff with the knowledge needed to maintain compliance and drive continuous improvement.
Whether you are in pharmaceuticals, biotechnology, medical devices, or environmental management, I can help your business meet the highest quality standards.