Covid-19 hastens the need for new clinical trials, staff & sites. Join our Global Networking Series to explore the Online Approval Process of clinical trials

Workshop on the responsibilities of the CRA, CTA and CRC during the initial phases of the clinical trial: Site Selection, Study Feasibility Assessment, Pre-study Site Qualification Visit and Site Initiation Visit.

3 KEY ARGUMENTS WHY MEDICAL WRITING CAREERS IN THE CLINICAL TRIALS INDUSTRY ARE OF HIGH INTEREST IF YOU HAVE A PhD OR MD/DVM/BDS/PharmD DEGREE

Pharma Regulatory Affairs Jobs - How to break in - Global networking event series. Talk to an expert   Meet by Zoom a seasoned mentor to learn about the exciting careers in the Pharmacetical Regulatory Affairs and get answers to all your questions    ...

La Réglementation Algérienne sur la recherche clinique est basée sur la Loi n°85-05, l’Arrêté n°387 du 31 Juillet 2006 relatif aux essais cliniques qui définit les conditions dans lesquelles s’effectuent les essais cliniques sur l’être humain

Clinical trial outcomes selected for evaluation must address trial objectives, irrespective of their association with the interventions. Endpoints are specific measures of these outcomes and their selection is a complex process.

Pharmacometric PK/PD modelling and simulation are a powerful tool in therapeutic drug development decision-making to understand the dose-response relationship in order to determine how much and how frequently to administer a treatment.

When COVID-19 emerged, clinical trials were given guidelines not set in stone in nation-wide regulatory changes for times of emergency.

RA staff ensure compliance with applicable regulations, clinical trials, regulatory submissions, production, marketing, distribution & post-market surveillance

WHO and INSERM launch clinical trials on the 4 most promising coronavirus treatments