Plant Solopharm is an example of production in accordance with GMP standards!

From 22nd to 23rd of May in "Novotel St. Petersburg" Italian validation company DOC srl held a training seminar “Validation life-cycle of critical utilities for pharmaceutical manufacturing: pharmaceutical water and steam and process gases” with a full overview of cGMP requirements of the European Union (EMA), United States (FDA / USP) and international cGMP (WHO and PIC/S) validation. After the seminar the participants visited plant Solopharm where they looked at the new modern production facilities and shared experiences of the validation (qualification) of pharmaceutical industries for compliance with Russian and international requirements.