by In2Pharma | Nov 6, 2019 | News
Belgium As a precaution, the European Medicines Agency (EMA) and European medicines authorities asked marketing authorisation holders in October 2019 to perform a risk assessment on the presence of nitrosamines. The Federal Agency for Medicines and Health Products...
by In2Pharma | Nov 4, 2019 | News
Europe EMA’s human medicines committee (CHMP) is requesting as a matter of precaution that marketing authorization holders (MAHs) for human medicines containing chemically synthesized active substances review their medicines for the possible presence of nitrosamines...
