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Regulatory Affairs - 3R Pharma Consulting - reducing regulatory risk
pharmaceutical products, medicines, regulatory affairs, application procedures, Chemistry Manufacturing Control (CMC), Stability Testing, Quality by Design, Release (RTR), Process Analytical Technology (PAT), Quality Control, Good Manufacturing Practice (GMP), Quality Assurance, Inspection, Anti-counterfeiting, Qualified Person (QP), CTD Module 3, training, courses
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Eviva Pharma Ltd
Jim Rennie established Eviva in February 2008 to provide pharmaceutical consultancy and interim management services to the pharmaceutical industry, and particularly for Hitech/Biotech or Virtual companies on a very flexible basis.
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