If you have any further questions or enquiries please contact: service@transtissue.com
- GMP implementation production & quality assurance for pharmaceuticals / medical devices
- GMP-compliant validation (documentation, realization)
- Regulatory support for medical devices (up to class III)
- Audits & documentation
- Set-up of quality management system (ISO 9001, ISO 13485, CMDCAS)
- Support for clinical studies (e.g. study design, documentation and monitoring for medical devices)
