SANTA SA, Braşov

SANOSAN's research and development team has the goal of delivering several new products every year. Expert professionals dedicate their attention on generic drug formulation, analytical development, pilot scale production and stability trials ensuring industrial application. SANOSAN's in-house regulatory affairs specialists compile CTD-format dossiers according to the latest EU regulations, opening the door to international out-licensing of all new developments. Your business partner in CONTRACT MANUFACTURING: SANOSAN Pharmaceuticals can fulfil your outsourcing needs for compressed tablets on the following areas: Pilot batch production Contract manufacturing of industrial batches Re-control and release of commercial batches By providing high quality products and conscientious service at fair prices we enable our customers to develop their businesses by doing what they do best: selling and marketing. Ensuring quality in every process is a day- to-day activity at SANOSAN. Quality control is guaranteed by using the latest technologies according to the European and the United States Pharmacopoeias. SANOSAN is under the process of obtaining the main accreditations from the Romanian and European regulatory authorities for the following areas: Pharmaceutical quality control analysis Pharmacological substance determinations Microbiological testings SANOSAN offers clinical research services in Romania through its partners for: Bioequivalence studies Clinical trials phase II-IV SANOSAN Pharma Consulting's experts specialize on the following main areas "Imagination is more important than knowledge" - A.Einstein GMP & GLP sites - Pharmaceutical production site design - Production processes & equipment - QC processes & equipment Product development & product registration in Central and Eastern Europe Pharmaceutical Intellectual Property (PIP) marketing - Out-licensing - In-licensing Feasibility studies on investments and pre-marketing studies