SeerPharma has extensive experience auditing organisations to TGA, FDA, EU, PIC/S, APVMA and ISO regulations and standards. This experience includes auditing Quality Management and Computer Systems used throughout the product life cycle, from pre-clinical testing to commercialisation and distribution.
SeerPharma is routinely engaged to support and ready to help you with:
- Supplier Audits
- Internal Audits
- Due Diligence Audits
- Gap Assessments
- Preparing and Responding to Regulatory or Notified Body Inspections
