Category: Articles

“Artificial Intelligence (AI) in Pharmacovigilance:do we really need it…?”Part 1: The Technicalities“Artificial Intelligence” is one of the most used buzzwords in these days.However, there seems to be a lack of clarity about the meaning of terms such as “artificial intelligence...

“EUCROF/eClinical Forum’s eConsent Implementation Guide –TOPRA Awards Finalist 2021″The EUCROF and eClinical Forum Electronic Informed Consent (eConsent) Joint Task Force are pleased announce that the eConsent Implementation Guide they published earlier this year has been recognized by TOPRA and is...

“EUCROF presented at EMA/GCP IWG workshop on AI in Clinical Research”Fiona Maini represented EUCROF at a two day workshop with the EMA/GCP IWG on AI in Clinical Research. Fiona presented on Ethical and Trustworthy AI and the draft proposal on...

EUCROF is very pleased to post its third Podcast on the topic:“eConsent​”How will eConsent transform your clinical trial? Tune in to the EUCROF Podcast on eConsent, and explore stakeholder perspectives on how eConsent transforms clinical trials from our guest speakers. Find...

2022 European Conference on Clinical ResearchLet’s meet in Madrid!EUCROF is pleased to invite you to browse through the link of the EUCROF Conference in Madrid, on 7 – 8 February 20226th European Conference on Clinical ResearchJune 18, 2021

Partnering for Patients Conference28 May 2021On Friday 28 May 2021, the Greek Patients Association, the Hellenic Association of CROs (HACRO), the Pharma Innovation Forum Greece, the Hellenic Association of Pharmaceutical Companies (SFEE), the Panhellenic Union of Pharmaceutical Industry (PEF), together...

International Clinical Trials Day20 May 2021The International Clinical Trials Day is set on 20th May as a celebration of James Lind’s very first clinical trial.Whilst working as a surgeon on a ship, Dr. James Lind (1716-1794) was appalled by the...

Press Release17 March 2021The European CRO Federation (EUCROF), announces the submission for approval by the Data Protection Authorities of the 27 EU Member States and the European Data Protection Board, of its GDPR Code of Conduct for Service Providers in...

eConsent Implementation GuideThe EUCROF and eClinical Forum Electronic Informed Consent (eConsent) Joint Task Force are pleased to announce the publication of the eConsent Implementation Guide (version 1). The joint task force was formed in 2019 with a view to look...

The archiving of clinical trial records is a required process that is in need of future direction to meet current business models as well as regulatory and legal expectations.  A group of industry experts coalesced under EUCROF and the eClinical...