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Established in 1997 DOC is a company specialising in providing consultancy, qualification, and validation services to Pharmaceutical Industries, Engineering, and Equipment manufacturing companies. Being a communication platform, DOC plays the role of the System Integrator acting between the cGMP compliance requirements and the final users.

Together, these divisions enable DOC meet the ever-changing needs of our clients and to provide turn-key support starting from the User Requirement Preparation for a new Equipment or System start-up to the qualification life cycle of the finished pharmaceutical drug form.  Besides the continuous investment in the most precious resource, our People, allowing us to expand, day after day, DOC Know-how and Expertise in Pharmaceutical Operations provide top-quality services in a Market constantly evolving.