European Pharmaceutical Review

JUNE 27, 2023

Riding on the momentum of the first faecal microbiota product approved for C. At MaaT Pharma our donor-derived products are made through pooling (ie, mixing multiple donors), thus achieving a higher overall richness and standardisation of the resulting drug product. coli strains in the gut”.

Food and Drug Administration 103

Food and Drug Administration Manufacturing Medicine Pharma 103

Legacy MEDSearch

JULY 21, 2023

This milestone indicates a new era for millions of women suffering from SUI, and results of this clinical study will contribute to the design and implementation of UroMems’ pivotal clinical trial in Europe and the U.S. STeP participation does not imply product authorization. Food and Drug Administration).

Food and Drug Administration 52

Food and Drug Administration Patients Safety Recruitment 52

Medgadget

MAY 3, 2023

AI-driven technologies are helping to automate mundane tasks, freeing up clinicians to focus on more complex clinical decisions. Medgadget: What are the main challenges you face today in medical/clinical imaging? AI is increasingly being used in healthcare to reduce clinician workloads and improve patient outcomes.

Healthcare 81

Healthcare Healthcare Leads Medical 81