DOC Services are divided into three main functional areas of business, which each include various subdivisions.
Together, these divisions enable us to meet the changing needs of our clients, providing them with turnkey support, from the User Requirement Preparation for a new Equipment or System start-up, to the qualification life cycle of the finished pharmaceutical drug form. Our continous investment in people, our most important resource, allows us to expand our knowledge and expertise in Pharmaceutical Operations, and provide services at the highest level in a market that's constantly evolving.
Equipment & System Division
At DOC, we have all the experience and expertise required for qualification and validation.
Products & Process Division
Our dedicated team offers a wide range of services.
We provide a wide range of consultancy services that are focused on developing robust and lasting cGMP quality and regulatory compliance.