ATechno designs and builds its own works for the last time and their maintenance can be carried out more effectively to ensure its durability. For that ATechno also discusses activities validation, activities necessary to operate safely and to ensure the Customer installations. This service can be provided regardless of the realization of the work.

Practicality

It will coordinate and check operations to achieve an end to endorsements and certification activities, defining in advance whenever technical operations datas, in order to be able to control costs and ensure it meets the estimates.

Validation of equipment (pharmaceuticals)

The purpose is to show that a particular process, or subprocess, is repeatable and it provide a product whose features meet the specifications defined.
The validation is a standard of good manufacturing or Good Manufacturing Practice (GMP) to which the pharmaceutical industry should refer to establish a quality system effective.

Validation of the plant (pharmaceuticals)

As for the validation of the equipment, the plant validation must ensure repeatability of the process. The repeatability is also related to the ability of the process of making a product that complies with specific reference whose limits are declared to the Ministries of Health of the countries to which the drug is intended.

Note that the success of activities related to the validation (and the own correct documentation) is binding on the approval of the drug at the Ministries of Health, and then for the release on the market for lots of product.