Product description

TECNALIA, experts in Pharmaceutical Development, Scale-up & Pilot Batches Manufacturing, Clinical Trials and Contract


• 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.).
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