All posts by Paola Sangiovanni

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About Paola Sangiovanni

Partner of GITTI and Partners. Seasoned transactional and regulatory legal counsel with a thorough understanding of the life sciences industry.

Re-Use of Research Data

It may now be easier for private companies to re-use research data generated by the public sector. Thanks to Italian legislative decree no. 200 of 2021 implementing Directive (EU) 2019/1024 of the European Parliament and of the Council of 20 June 2019 on open data and the re-use of public sector information, re-use of research data – whether for commercial or non-commercial purposes – may be carried out so long as intellectual property rights and privacy rights are respected.

In other words, if research data is anonymized and does not include intellectual property, free re-use is possible whenever such research data is generated from public funding and made available by researchers or research institutions through public data bases. Research data must comply with Findability, Accessibility, Interoperability, Reusability (FAIR) principles.

What is “research data”? Research data means “documents in a digital form, other than scientific publications, which are collected or produced in the course of scientific research activities and are used as evidence in the research process, or are commonly accepted in the research community as necessary to validate research findings and results”.

Are you in need of an example? “Research data includes statistics, results of experiments, measurements, observations resulting from fieldwork, survey results, interview recordings and images. It also includes meta-data, specifications and other digital objects. Research data is different from scientific articles reporting and commenting on findings resulting from their scientific research” (whereas no. 27 of the 2019/1024 Directive).

Certain scholars have pointed out how the principle of scientific open data is framed in terms that are too restrictive and continue to clash with intellectual property rights, database and algorithm protection.

While the push for reuse of research data may appear timid at this point in time, the EU seems in any case determined to continue its open data agenda through the Data Governance Act.

Only 1 Week until Go Live of EU-Wide Clinical Trials Information System

Remember the Clinical Trials Regulation? Much time has passed since its publication in 2014. No worries if your memory fails you: we have discussed the Clinical Trial Regulation at length in this article appeared on the Indian Law Journal of Law and Technology. If you prefer a shorter summary, you may read here what the European Medicines Agency has prepared for you.

The actual entry into force of the Clinical Trials Regulation depended on confirmation of full functionality of the Clinical Trials Information System (CTIS) through an independent audit, which occurred on April 21, 2021. Now, the go-live date for the CTIS will be on January 31, 2022. Information on the go live planning can be found here.

The Clinical Trials Regulation was born to address the prior directive’s shortcomings, and particularly to target the goals of harmonization and simplification in this field, also with a view of making Europe a competitive region in the global clinical trials market. Good luck to the CTIS: we hope the Clinical Trials Regulation keeps its promises!

Much HEALTH and happy holidays to you all!

As the second year of the pandemic draws to a close, it is easy to find reasons to complain: they sometimes come conveniently arranged in alphabetical order (Delta, Omicron…)!

But we also want to remember the many things we are grateful for: vaccines, for example, but especially your friendship and support in 2021.

May 2022 be a good year to you and your loved ones. May you face 2022 armed with hope, courage, empathy, resilience and joy.

The Gitti and Partners life sciences team.

U.S. vs Italy Healthcare Fraud Laws

I am happy to announce that the article that Marc Raspanti and Pamela Coyle Brecht of Pietragallo Gordon Alfano Bosick & Raspanti, LLP and I have authored has been published in Compliance Today: https://bit.ly/3Cs9HOI , a publication of the Health Care Compliance Association.
This is Part 1 of a three-part series discussing the similarities and differences between the U.S. and Italian healthcare fraud, waste, and abuse laws.
Keep an eye out for Part 2 and Part 3 of this series that will be published in the December and January issues of Compliance Today.

Our Article on Clinical Trial Legislation Is Out

We are happy to announce that our article on “Drug Clinical Trials Legislation in the European Union” has been published on the Indian Journal of Law and Technology (https://www.ijlt.in/).

You may read it here or here.

The purpose of the article is to illustrate the basic tenets of European Union law on clinical trials. Such body of law has been progressively harmonized in the European Union over the years with the aim of subjecting interventional clinical trials conducted in any of the 27 European Union Member States to identical rules.

The article initially describes the reasons why clinical trials are important to measure the safety, efficacy and cost-effectiveness of innovative medical treatment. It then continues by illustrating the scope and basic principles of the current EU Regulation, as well as its main changes over the previous legislation. Further, the article explains the requirements of the scientific and the ethical approvals of a clinical trial application. Lastly, the authors focus
on the patients’ consent to the enrollment in a clinical trial, as well as to the patients’ separate consent to the processing of their personal data