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Tech Transfer Think Tank: 4T - Meeting - 22 May 20...
This year conference will be on May 22 at Kilometrorosso, Via Stezzano 87, Bergamo, Italy.

IFIB 2015 - 5th Annual conference, 24-25 September...
The IFIB (Italian Forum for Industrial Biotechnology and Bioeconomy) annual conference and partnering event will be held in Lodi on 24-25 September 20...

Intesa Sanpaolo Biotech and Healthcare Investment...
The Biotech and Healthcare-Medical Device start-up arena meeting will be held on 21 and 22 April 2015 in Milano.

Sofinnova Renewable Chemistry Start-up Award
Sofinnova Start-up Award recognises the most promising renewable chemistry start-up The Top 5 companies will be selected by popular vote online and th...

Would you improve your probability of success?
Do you have an idea or a new technology you would evaluate?
Are you sure that your product gets to market as quickly and efficiently as possible?
An European Medicines Agency submission is not an easy task. It is a time-consuming, need experienced people, planning capabilities and strong project management. We offer our support in order reduce time, improve quality of submission and consequently chance of success.
Without a strategy you are not able to identify challanges, allocate resources, define timeline and respect dedlines.
A good Regulatory strategy oversee the whole development process, helping you to save time and money, improving chance of success.
Products and technologies available for license or sale
We offer a full range of quality systems and external activities review and audits. Our audits are conducted by experienced professionals who produce audit reports with the highest levels of accuracy and consistency in respect of timelines. We are priced competitively and we are qucik in activation.
We could evaluate your technology or idea and provide you a report with an in dept analysis of:
1) The technical merits and challenges of your invention;
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Focus on Biosimilars
Regulatory service for development and approval of biosimilars in the EU
Advice on regulatory specific strategy for EU biosimilars.
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