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)