Scopes of action


We provide help and support to pharmaceutical manufacturers to comply with national, EU regulatory requirements.

  • OTC , EFP , self-health care
  • Medical devices in accordance with ISO 13485:2016

Market analysis

We collaborate and get involved in the identification of the target markets, stakeholders , products and services for each business area, in the strategic definition and the financial model.

  • Licensing IN and Licensing OUT: We collaborate both in the search for products and for the search for the best partners .
  • License: We help in applying for all the necessary licences for the correct development of your pharmaceutical project.

Pharmaceutical Consulting Engineering and GMP

End Engineering Design ( FEED ) Study, Turnkey Construction Design

  • GMP projects: We have qualification and validation services to ensure that your facilities, equipment and services comply with existing regulations.

Human Resources and Training

Selection and recruitment of qualified personnel. Also in customized In-Company training.

Regulation affair

Definition, implementation and monitoring of regulatory strategies and procedures to achieve the registration of your products efficiently.