A permanent dialogue with you
We believe in the importance of the real-time reconciliation of risk assessment and test results. No two customers are the same. We respond individually to your requirements and needs in order to achieve the best possible result.
Our concept
- Risk-based approach in line with GAMP5
- Full traceability
- Design, assembly, commissioning and qualification from a single source
- Qualification based on the V-model (GAMP 5)
Your benefits
- Long experience: 98% of all Medtech systems qualified by teamtechnik
- Provided documents follow the GAMP, EU GMP, ICH and FDA guidelines and regulations
- Many functions are already covered by the standard platform qualification
- Qualification service can be adapted to your needs
- All from a single source means less interfaces
Changes must be transparent. We are familiar with the high demands placed on engineering processes in the pharmaceutical environment. Our activities are geared towards them - from the change order to release and requalification.
These are our standards
- Machinery Directive (2006/42/EC)
- Quality management (ISO 9001:2015)
- Environmental management (ISO 14001:2015)
- Good Manufacturing Practice (GMP - EU Guidelines for Good Manufacturing Practice Medicinal Products for Human and Veterinary Use - Annex 15)
- Good Automated Manufacturing Practice (GAMP 5)
Get in touch with our experts

HQ reception
Would you like to contact teamtechnik online?
Then use our online contact form!

HQ reception
Would you like to contact teamtechnik online?
Then use our online contact form!
News
Fairs & Events
Downloads
Medtech – Palletizing systems (EN)
PDF / 843.48 kB
Medtech – Palletizing systems (EN)
PDF / 843.48 kB
Medtech – Feeder Systems (EN)
PDF / 780.07 kB
Medtech – Feeder Systems (EN)
PDF / 780.07 kB
Medtech - Brochure (EN)
PDF / 2.82 MB
Medtech - Brochure (EN)
PDF / 2.82 MB