3R PHARMA CONSULTING provides cost-effective, timely solutions to challenges in pharmaceutical development across Europe, the US and the rest of world. Advice on Quality/CMC aspects of pharmaceutical development 3R PHARMA CONSULTING offers regulatory advice and services covering quality-related aspects of pharmaceutical development. 3R PHARMA CONSULTING strives for fast submissions and approvals of applications. GMP audits/mock inspections 3R PHARMA CONSULTING conducts internal inspections, pre-approval mock inspections, as well as GMP Audits of API manufacturers and manufacturers of finished dosage forms. Evaluation of stability studies Clients are provided with scientific and technical advice, as well as stability reports and summaries which include statistical analysis of stability data. Courses and workshops on quality aspects 3R PHARMA CONSULTING offers basic introductory courses, as well as specialised workshops and training courses, tailored to the needs of the customer. These courses can either be organised in-house or externally.