Creating impact.
Together.
Learn how
Creating impact.
Together.
Learn how

We are Pharmabooks Regulatory and Scientific Services, an integrated end to end service provider, across different life sciences sectors, from product development to product commercialization covering a plethora of therapeutic and consumer health areas. Our passion, experience and deep know how of the scientific and pharmaceutical industry for effective and safe products as well as the need of our partners for value add, product supply and competence, are the cornerstones of our activities.

Who are we talking toWe act responsibly and professionally with Industry and Companies

Consultants

“Wherever the art of medicine is loved, there is also a love of humanity.”

Hippocrates

What we do

Product Development is the key to successful product registration and approval. It is the question we always ask our customers “What is your goal?” and then we pave the strategy and bring in the formulation and analytical knowledge to reach this goal. External pressures of the globalized market in a highly competitive environment, rapid technological changes and short product lifecycles have made new product development an important strategy for companies.

We engage with our clients to achieve positive pharmaceutical regulatory outcomes by using a modern, scientific approach as the drivers of success. We use our deep exprerience, from pre- through post-approval processes, of world wide product registrations through complex registration procedures.Managing medicinal product registration files, preparing, editing and maintaining the documents to go along with them is our core competence.

No project will run efficiently unless it is managed effectively. Companies usually lose a lot of valuable time, staff energy and money because projects are poorly managed. We are flexible, have deep know-how of the industry sector and we are able to liaise with the different departments (R&D, manufacturing department, QC, QA, RA, Marketing and pricing) to help you reach your target launch dates. We can effectively facilitate your process and save you time and effort with new and existing projects.

Through our strong and extensive network of professionals in strategic geographical locations, we seek to provide the best fit for your next product.

provide local support and representation in Greece for regulatory and legal compliance with the Authorities or Ministry of Health via direct or in person communication.

Safety is crucial for patients, manufacturers and Regulatory Bodies and should be monitored throughout the product’s lifecycle.

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