Polpharma’s R&D analytical laboratory in Sieradz specializes in the development and validation of analytical methods for starting materials and finished products, their stability testing and development of registration documentation. Our team of analytical experts provides experience, efficiency and technical proficiency in the development/validation of GMP analytical methodology for your various non-sterile dosage forms – liquid, semi-solid or soft gelatine capsules.
One of our latest challenges is the development of innovative inhalation products.
Pilot plant is equipped with a number of infrastructure elements necessary for working with highly active substances.
For details on our contract manufacturing offer, please contact Ms Patrycja Szwarc and Anna Marciniak.