ServoTech GmbH

Individual machines are often joined together to form an integrated plant (linked facilities) in an industrial concern. When this occurs, the integrated plant must recieve CE certification.

These steps are required to assess the integrated plant's compliance:

• Individual machines must undergo a technical inspection for safety.
• Documents delivered with the individual machines must be checked.
• A primary risk assessment for potential dangers must be accomplished.
• A primary operator's manual which integrates documentation from the individual machines must be created.
• Create a conformity declaration for the complete plant and attach the CE certificate.

With our CE Advice, ServoTech primarliy supports production operations that are concerned with the CE certification and work safety standards.

In national and international regulations, employee training is designated as the most important instrument in quality assurance. ServoTech supports you with training about Good Manufacturing
Practice, so that your employees are able to understand the main GMP concepts, can easily move about in the GMP environment, and can develop GMP projects in a simpler and safer manner.

How do we work for you? Simply put: You give us your raw data like parts lists, technical drawings, photos, etc., and we create documents with information that is suited to your target group. We search for, and insert, missing information.

A team of qualified editors, illustrators, layout experts, among others, are available to ServoTech Documentation GmbH, for this purpose. We create documents according to your wishes: whether printed, bound, or burned to CD or DVD.

We always deliver first-class results for your company image.

ServoTech supports manufactures of pharmaceutical machines and systems as well as pharmaceutical firms in their qualification and validation activities in the pharmaceutical, medical technology, diagnostic, cosmetic and food industries. Of course we also perform re‐qualification of older systems or support you in supplier qualification, URS creation, and writing FS documents.