Decades of experience in pharmaceutical analyses and compliance with GMP, EMA, and FDA guidelines.
Analytical Services
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Our Analytical Development department offers comprehensive analytical services for pharmaceutical excellence
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.
Why choose Tiofarma for analytical services?
Utilization of cutting-edge analytical tools and methodologies.
Close coordination with clients to ensure high-quality and timely results.
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.
Pharmaceutical analyses
Our Analytical Development department specializes in developing comprehensive pharmaceutical analyses, covering APIs, finished products, stability testing, and validation tests for processes and cleaning. Equipped with both traditional and advanced analytical techniques, our laboratory excels in handling nasal sprays and semi-solids.
Quality and compliance
All analyses are performed in accordance with strict regulatory standards, including USP, BP, and EP monographs, and are compliant with the latest GMP, EMA, and FDA guidelines. We are committed to continuous improvement and expanding our analytical knowledge.
