PHARMINNOVA P.C. is an experienced, consulting group focused on the global pharmaceutical industry, covering services for an extensive portfolio of medicinal products.
We are always up to date with current legislation, regulatory requirements, industry initiatives and interpretations of the regulations and scientific guidelines. PHARMINNOVA scientific staff and collaborating experts will ensure that you have access to the right level of skills and experience, along with the flexibility that your project requires. Having previous work experience inside regulatory agencies at the national and international level, as well as within pharma industry, bring a unique level of insight and expertise to our work. Our ability to respond quickly and flexibly to ever-changing client needs in a complex regulatory environment combined with a consistent and dedicated commitment to quality services are important elements of advantage.
PHARMINNOVA experts, having vast experience in a variety of areas, such as strategic and scientific advice, regulatory affairs, business and product development, dossier compilation etc, develop creative approaches to assist you in bringing your products to any market.
The aim of PHARMINNOVA is to provide our customers with a reliable, flexible and effective strategic regulatory and scientific affairs service, covering all stages of pharmaceutical development and authorisation process in a timely and cost-effective manner. Our mission is to assist pharmaceutical companies in rationalizing drug development and we use innovative approaches and services, in order to translate the scientific knowledge into tangible benefits for patient care.
Guiding you all the way up
PHARMINNOVA is in close collaboration with experienced and reliable partners worldwide (including CROs, CDMOs, Pharma Companies, as well as with Academic Institutions), utilized on a per-project basis.
Our clients include many pharmaceutical companies around the world.