Medicine Quality Monitoring Globe

by Global Pharmacovigilance
3rd April 2020 • 0 comments
28th June 2019 • 0 comments

Spontaneous Reporting

by Maximillian Schurer, Global Pharmacovigilance
30th April 2019 • comment
17th April 2019 • 3 comments

Responding to the growing mandate for researchers to share their clinical data, WWARN is joining with partners to host a 3-day workshop in January sponsored by the British Council’s Newton Researcher Links Programme in order to develop the skills and network needed to produce high quality data capable of maximising the impact of initial findings.

19th October 2017 • 0 comments
7th August 2017 • 0 comments

In 2012, the International Federation of Obstetrics and Gynecology (FIGO) produced a chart detailing recommended dosages of misoprostol when used alone, for a variety of obstetric and gynecologic indications. In light of new evidence and through expert deliberation, this chart has now been revised and expanded. The present commentary explain the changes and the decisions made. 

17th July 2017 • comment

The Cups or Cash for Girls (CCg) Trial is currently being conducted in Western Kenya. This trial is investigating whether giving school girls a menstrual cup, cash transfer, or both, has an impact on various deleterious outcomes. This trial offers a unique perspective on safety monitoring and this article discusses why safety monitoring is important in such a trial and how it is being tackled.

14th July 2017 • comment

Pharmacovigilance in pregnancy

by Global Pharmacovigilance
6th July 2017 • 0 comments

The Cochrane Adverse Effects Methods Group presented a webinar on 'How to Overcome the Challenges of Reviewing Adverse Effects'. View an edited version of this webinar or download the slides.

8th June 2017 • 0 comments

DSMBs and clinical trial safety

by Global Pharmacovigilance

The Data Safety and Monitoring Board (DSMB) or Data Monitoring Committee (DMC – these are synonymous terms) is a group of individuals put together by the sponsor or CRO (if contracted out) with relevant expertise to carry out the important role of monitoring the safety of a clinical trial study.

1st June 2017 • 0 comments

Building Teratovigilance Capacity in Africa

by Global Pharmacovigilance
13th March 2017 • 0 comments

Trying to identify genetic biomarkers of nevirapine hypersensitivity.

28th February 2017 • 0 comments