Services

Equipment & System Division

Perfect organization and executation for qualification and validation

Equipment and Systems that have a direct impact on the pharmaceutical drug quality or medical devices by GMP Law should be validated in order to demonstrate the expected performance in a reproducible way.

DOC Equipment & System Division can organize and execute qualification and validation of new or in use existing Systems; the several activities are fully traced and documented applying the Validation Life-Cycle from the User requirements to the Validation maintenance.

Product & Process Division

Dedicated Team for able to offer a wide range of services

DOC global offers are not only limited to the qualification of equipment and systems; thanks to a dedicated Team of Project Managers consisting of Biologists and Biotechnologists with consolidated experience on the field, DOC is able to offer a wide range of services that encompass the Development and Validation of Sterile and non-Sterile Processes up to the Qualification of Pharmaceutical and Cosmetic finished forms.

For all these activities, DOC is fully capable of handling any kind of product formulation from the Active Pharmaceutical Ingredients (APIs) up to Cytotoxic and Controlled drug substances and their precursors. The laboratory structure in which our tests and studies are executed is GMP, GLP qualified and FDA approved since 1997.

Our Process Validations take into consideration the reproduction of the actual manufacturing operation from the small scale of Clinical and R&D processes to long and complex process campaigns.

Consultancy & Training

Always tailored for your needs

DOC provides training and seminar, projected and thought by its expert team.
Each module is customizable and tailored for the needs of its clients. 
Thanks to his long experience, DOC is also able to offer a wide range of consultancy services to avoid 
or react at crisis or diseases of your business.