Due to the current pandemic, the BIO International Convention will transition to an innovative, virtual event format, BIO Digital for 2020.
Nubilaria Srl is an Information Technology (IT) company founded in 1999. Our company has its origins in the design, management and distribution of complex database systems and innovative IT services under strict international security policies.
A group of qualified and experienced professionals are the fundamentals of our success. They are the beating heart and the creative spirit of our company. Together we are constantly looking for innovative solutions.
Nubilaria’s Clinical business unit started operating in 2009 and has since been praised by many pharmaceutical industry leaders for the quality of its services. The Clinical Data Management services provided by the company support the entire data lifecycle.
EDC and Clinical Data Management Software
Our eClinical platform is suitable for any type of clinical study, for both human health care and animal health care, within a secure and validated environment.
ACTide by Nubilaria
ACTide EDC bundles-up with ACTide eCRF, our intuitive user interface, and ACTide Designer our eCRF configurator: The all-in-one solution.
ACTide in two different configurations to accommodate client requirements
Self-provisioning: for independent users who need a cutting-edge service to support fast & accurate prototype turn arounds
Full-service: for users who need to rely on our expertise to develop their eClinical solution without limits in complexity or scale
Whatever configuration you choose, we are always available to support you and we go the extra-mile to ensure the success of your study.
Nubilaria ACTide benefits for CROs and Clinical Centres
Some of the features ACTide’s users (CROs and Clinical Centres) appreciate most are the quick and easy eCRF setup, the significant cost reductions, the monthly subscription fees, the non-profit/orphan diseases special pricing, a peace of mind on software compliance, easy auditing, study level validation tools and the native multilingual interface for multi-national trials.
Compliance & Certifications
ACTide eCRF is fully validated and developed in compliance with:
• US FDA – 21 CFR Part 11
• EU GMP Annex 11
• GAMP 5
• GCP – Guideline for Good Clinical Practice
• GDPR Compliant
Nubilaria is certified:
• ISO 9001:2015
• ISO/IEC 27001:2013
Major announcement for Researchers and Health Professionals in Europe who wish to commit to the fight against Covid-19: a powerful acceleration of research to gain understanding and facts is required.
Nubilaria ACTide will be attending the virtual Outsourcing in Clinical Trials experience, presenting at our virtual booth.
Nubilaria delivers the ACTide EDC web platform free of charge for:
Actide is pleased to announce that it will be attending the 5th European Conference for Clinical Research in Amsterdam, the Netherlands on 10-11 February.
ACTide will be attending CPhI worldwide on 5th – 7th November 2019 at Frankfurt, Germany.
ACTide is to attend PhUSE EU Connect 2019, which will be taking place from 10 to 13 November in Amsterdam, The Netherlands.