At Tiofarma, we specialize in pharmaceutical analyses, including raw materials, finished products, stability, and validation tests for nasal sprays, creams, and ointments.

Our Analytical Development department bridges our R&D facility, customers, and QC laboratory.

With over three decades of experience and compliance with GMP, EMA, and FDA guidelines, Tiofarma specializes in a broad range of pharmaceutical analyses and ensures to be a trusted partner for analytical excellence.

Choose Tiofarma for analytical services when you need proven expertise, advanced technology, and a collaborative approach. With decades of experience and full compliance with GMP, EMA, and FDA guidelines, we combine state-of-the-art analytical tools with close client coordination to deliver reliable, high-quality results on time.

State-of-the-Art infrastructure

Our laboratory is equipped with a wide range of state-of-the-art analysis equipment, including (u)HPLC systems with mass spectrometry and UV detection, particle/droplet size via optical microscopy and/or laser diffraction, Rheology/ viscosity and IVRT. Result processing is managed using a mature LIMS system.

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