IDIFARMA has obtained an extension of its authorization as a GMP clinical manufacturer by the Spanish Medicines Agency (AEMPS) to include new dosage forms. The expanded GMP capabilities allow for the manufacture of powders for oral use (including powders for oral solutions and suspensions), as well as tablets and hard capsules. IDIFARMA has also adapted its lab authorization to the new European format for manufacturing, including GMP over-encapsulation to blind solid dosage forms for double-blin...