SeerPharma leverages decades of experience providing guidance and support to help organisations achieve and maintain a state of compliance with TGA, FDA, EU, PIC/S, APVMA and ISO regulations and standards. You can count on SeerPharma to provide expert GxP compliance advice to pharmaceutical, medical device, and life sciences industries.
SeerPharma is routinely engaged to support and ready to help you with:
- Facility design and engineering projects, including services
- GxP licensing and audits/inspections
- Best-practice compliance (documentation, processes etc.)
- Equipment & service qualification
- Personnel training
- Process validation and Computerised System Validation (CSV) including Computer Software Assurance (CSA)
