regulatory authorities

Pharmassess Audit Reports Marketing Authorisation Holders (MAH) are required to audit their suppliers at least every 3 years to ensure that manufacturing processes comply with Good Manufacturing Practice (GMP). These audits can be carried out by the MAH themselves or someone acting on their behalf. A more economical and efficient […]

Rephine Audit Reports – Good Manufacturing Practice Pharmassess – Pharmaceutical ...

 in Certificati GMP  con tag api sourcing / auditing / consultancy services provided / EMA / GMP / good manufacturing practice / ICH Q7 / MAA / MAH / marketing authorisation holders / MHRA / operational consultancy / pharmaceutical companies / pharmaceutical consultancy / pharmaceutical manufacturers / pharmassess / pharmassess audit reports / project management / Q9 standards / qp service / quality management system / regulatory affairs / regulatory authorities / regulatory services / rephine / third party GMP auditing / third party GMP audits / training di