WELCOME TO DOC

Experts in cGMP compliance

At DOC, we are experts in the complex world of cGMP regulations and technologies, exchanging knowledge and expertise with our clients worldwide.

 

We are experienced in working as partners with Pharma
and Biotech companies, C(D)MOs and OEMs.

 

We are leaders in cGMP consultancy, System Qualification & Process Validation globally.

 

We also have the vision to create Training & Educational Programs for Industry and Academia.

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Why DOC

We managed to build a leading reputation in life sciences industry through:

HISTORY & TRACK RECORD

We have over 25 years of successful experience, working with the leading Pharma groups all over the world.

FLEXIBILITY

All DOC solutions can be customised to suit our clients' unique requirements and SOPs in all validation lifecycle.

EXPERT TALENTS

At DOC, we have a high level of expertise and experience in all aspects of Systems Qualification and Process & Product Validation, including Training approaches.

PARTNERSHIP WITH EDUCATIONAL INSTITUTIONS

In partnership with renowned Italian universities, DOC has developed Masters Degree programmess for Pharmaceutical professionals and young graduates, offering them a structured framework in which to expand their knowledge.

GLOBAL CAPABILITIES

Via our network, we are able to provide services throughout the world, organising the talent and instrumentation for each individual project.

Discover Why

Masco Group

At Masco Group, we help life science companies master the manufacturing process and stay ahead of industry challenges. 
We are an international team of specialised companies, and over the last century, we've grown, tested and proven our design-build-install-service capabilities. Today, our expert teams continue to push for progress, with customised and integrated project delivery.

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