A solid basis for sustainable growth

With a new production facility in Wimsheim, Germany, CAMLOG has created the basis for future worldwide growth. Over 160 qualified employees and an ultra-modern infrastructure near Stuttgart guarantee that our success story will continue as the years unfold.

Our production facilities, on about 4,000 square meters, are among the most modern of their kind in the world. Even at the planning stage, we placed the greatest emphasis on building a production operation that not only meets all the requirements of the Medical Devices Law, but also conforms to international criteria – especially the stringent American regulations. High-tech manufacturing processes and constant quality assurance guarantee a consistently high level of quality.

Our consistent quality philosophy has been confirmed by certification of our process-oriented QM system under EN ISO 13485 and EN ISO 9001 standards, as well as the European Directive 93/42/EWG for medical devices.

For the sake of the environment

At CAMLOG, environmental responsibility in everything we do is more than lip service. The new production plant in Wimsheim was built in compliance with all current standards of environmental protection. Exhaust air from production, for instance, is not simply released outside, but used for heat generation. Naturally, our production facilities also meet the strictest German requirements.

Everything under the same roof

CAMLOG is convinced that future success in the implant market is closely related to the company’s own research and development efforts. For this reason we attach great importance to our in-house developments and scientifically proven products.

CAMLOG Biotechnologies in Basel, Switzerland, is responsible for research and development within the CAMLOG Group. Our R & D staff continuously work on new solutions for our modern implantology systems, accessories and instruments. They are constantly advancing CAMLOG products on the basis of current findings in science and technology.

Our R & D staff also pay particular attention to easy handling of our products, the use of biocompatible materials for their production, achieving excellence in manufacturing, and ensuring product quality control in the interest of patient and user safety.

We meet international standards

ALTATEC GmbH, the manufacturing arm of the CAMLOG Group, is subject to regulation of its quality assurance system under the EN/ISO 13485 standard at every stage of its operations. This standard specifies in detail all the criteria that must be met by the extensive quality assurance scheme relating to the company’s operations in order to be recognized. Naturally, ALTATEC complies fully with the standard. Quite correctly, medical products and devices must meet particularly strict requirements.

The CAMLOG Group ensures that the quality of its products and services meets the expectations of its customers. Our products comply with the basic requirements defined in the European laws and directives relating to medical devices with regard to product performances and patient safety. Besides EN/ISO 13485, ALTATEC has also been CE 0124 certified.

Nothing is left to chance

CAMLOG’s quality management consists of experienced staff with a core team that makes internal and external audits. Internal audits closely scrutinize the various product stages; external audits inspect our suppliers. In addition, a head-team has been established which is responsible for overall control of quality assurance.

Quality management is process-oriented, and quality assurance acts on a future-oriented basis. We control the quality of our products for consistency and sustainability in long-term tests made at our own locations with our own equipment.