Management Scientific Board Quality Assurance Unit Chemistry Department Formulation Manufacturing Department Minisynthesis Department Pharmacology Department Pharmacy Department Pilot Plant Department Quality Control and Research Analytics Department


  ORGANIZATION DRAFT > FORMULATION MANUFACTURING DEPT.

Certificate of GMP Compliance
GMP Certificate

The main task of the Formulation Manufacturing Department is to produce medicinal products. The manufacturing process includes both sterile (lyophilisates) and non-sterile products (capsules, soft shell).


The Formulation Manufacturing Department includes a Sales Unit, which is responsible for the sale of medicinal products manufactured in the Pharmaceutical Research Institute. It should be stressed that the manufacturing technology of all medicinal products currently produced has been developed and implemented by the Pharmaceutical Research Institute.


The manufacturing process is performed according to GMP principles (Good Manufacturing Practice). The quality of manufacturing process was confirmed by the Certificate of GMP Compliance No. GIF-IW-N-4022/15/09 issued by the Main Pharmaceutical Inspector (GIF - the Competent Authority of Poland).


The Formulation Manufacturing Department is also responsible for the adverse reaction monitoring and pharmacovigilance.

Staff:

  • Scientific staff - 2 persons (including 1 Ph.D.)
  • Technical staff - 4 persons

 Head:  Bozena Szyndler-Kaczynska, M.Sc.
 Phone:  (+48 22) 456 38 50
 Fax:  (+48 22) 456 39 23
 E-mail: