Lab &
Diagnostics
Filter plates, reaction vessels,
reagent boxes and racks.
Components AND assemblies FOR most demanding applications.
Single
source
From development and moldmaking to series production.
cleanroom
Production
Cleanroom manufacturing to DIN EN ISO Class 7 GMP Standard C.
CONTRACT MA-
NUFACTURING
Injection molding, assembly and finishing processes including mold repair.
CLIMATE-
PROTECTION
Climate targets validated by the independent Science Based Targets initiative (SBTi).
Certified to DIN EN
ISO 13485 and ISCC+
Fully automated
cleanroom production
In-house moldmaking
Resource conservation
through eco-design
Highest quality standards
for your application.
Whether for laboratories or diagnostics, the pharmaceutical industry or medical technology, individual components or multi-part assemblies, individual development or contract manufacturing: we have been producing plastic articles for the highest demands on cleanliness and hygiene since 2004. The strict regulations in the pharmaceutical industry and medical technology sector require customized article concepts and cleanroom production according to GMP (Good Manufacturing Practice) guidelines with corresponding documentation - certified according to DIN EN ISO 13485. From the initial idea to mass production, we handle development, tooling, manufacturing, assembly, and finishing—all in-house and in full compliance with GMP.
Real climate protection
also convinces our customers:
Sustainable extraction kits: Reaction vessels made of post-consumer recycled material.
"Pöppelmann FAMAC® has made a name for itself not only as a competent partner in the pharmaceutical-medical sector. With the PÖPPELMANN blue® initiative, the plastics specialist has made a clear commitment to more environmental and climate protection. Together, we have been able to show that this is both sensible and possible in the laboratory sector with its strict hygiene requirements."
Inga Irle, Senior Global Marketing and Product Manager Sample Technologies at QIAGEN
Optimally designed, stacked to save space – emissions saved.
"We are delighted about this successful cooperation and highly appreciate the overall strategy of our partner Pöppelmann FAMAC® to promote the use of recycled materials and to reduce greenhouse gas emissions as part of the PÖPPELMANN blue® initiative. For this and especially for the 'Air Force One' project, we awarded Pöppelmann FAMAC® second place in the 'Sustainability' category among all Dräger suppliers at the Dräger Supplier Awards"."
Kathrin Huth, Project Manager at Drägerwerk AG & Co. KGaA
CURRENT DEVELOPMENTS IN PHARMACEUTICALS & MEDICALS:
From development to series production: ALL from a single source.
One team, one ambition, one common goal: components and assemblies for your application at the highest level of quality. Our development expertise is focused on new technologies, products and markets. Quality, precision craftsmanship and high-tech manufacturing are the foundation of our technology leadership.
We make individual solutions possible.
MICHAEL
HOLLFELD
SALES
PHARMA & MEDICAL
MICHAEL
GIER
SALES
PHARMA & HEALTHCARE
STEFFEN
PREUSCHOFF
SALES
LAB & DIAGNOSTICS
FAQs
For which sectors is production carried out?
We manufacture plastic products for the laboratory and diagnostics, medical technology, and pharmaceutical and healthcare sectors.
What does contract manufacturing service include?
Our contract manufacturing services include product development, tooling, production, manual and fully automated assembly, finishing processes, and tool repairs—all in compliance with GMP and fully documented.
What materials are used?
We process standard thermoplastics as well as specialty pharmaceutical-grade and medical-grade plastics. Upon request, we also offer mass-balanced bio-based plastics or post-consumer recycled materials.
What certifications are available?
- DIN EN ISO 13485 for a systematic quality management system for medical devices
- ISCC+
- DIN EN ISO 45001 for an occupational health and safety management system
- DIN EN ISO 50001 for a systematic energy management system
- DIN EN ISO 14001 for a systematic environmental management system
To which standards is the cleanroom production certified?
Our cleanroom production is conducted in accordance with DIN EN ISO Class 7 and GMP Standard C. Our quality management system is certified to DIN EN ISO 13485.