Today, we are pleased to share the news that we have made available to download the first Ergomed Privacy Handbook Vol. I – Data Protection in Europe-based Clinical Trials.
This e-Book highlights data protection and privacy compliance matters that the Ergomed team has encountered in conducting numerous clinical trials on behalf of both EU and Non-EU Sponsors, all to support and encourage the building of solid legal and regulatory foundations.
Compliance with GDPR is a significant undertaking, particularly for specialty pharma and biotech companies with limited resources. Noncompliance can be highly costly in terms of clinical trial progress and heavy financial penalties. It is, therefore, essential for Sponsors to identify trusted partners who can help ensure that all aspects of clinical trials — and the data handling involved — are executed to the most current regulatory standards.
To download this e-book document, please click HERE.
The purpose of this document is to share the elements taken into consideration by Ergomed in its European Union (EU) General Data Protection Regulation (GDPR) compliance processes and to inform our stakeholders on the specifics of data protection in Europe-based clinical trials (with a particular focus on industry-specific privacy requirements).
At Ergomed, we understand that privacy compliance is a moving target as guidelines and practices evolve, and we constantly aim to:
- Proactively improve our current practices, policies, and procedures.
- Communicate Ergomed’s global privacy approach and introduce all colleagues to different phases of its implementation.
- Keep abreast of new guidelines and information based on the best practices and will be made available by the various data protection authorities.
We have an unwavering commitment to ensuring compliance with data protection requirements throughout our organization.
For any other inquires please get in touch with us via firstname.lastname@example.org