TECNALIA, experts in Pharmaceutical Development, Scale-up & Pilot Batches Manufacturing, Clinical Trials and Contract Manufacturing ANALYTICAL DEVELOPMENT • Monitoring of the first industrial manufacturing batches. • Characterization of raw materials according to Pharmacopoeia. • Development and validation of analytical techniques. • Quantification of active ingredients, impurities and degradation products in raw materials and medicines. • Transfer of analytical techniques. • In vitro dissolution profiles. TECNALIA´s Pharmaceutical Development Laboratory is accredited by the Spanish Medicines Agency (AEMPS) in Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). We offer solutions in several dosage forms formulation: • Solids (tablets, capsules, sachets, etc.) • Liquids (suspensions, solutions, syrups, etc.). • Semi-solids (gels, creams, ointments, etc.).
