Planning of Testing and Research Department (BK)

PERSONNEL:

Head: Bożenna Romatowska M.Sc., tel: +48 022 8413651
Joanna Borys M.Sc., tel: +48 022 8413651
Joanna Rękawek M.Sc., tel: +48 022 8413651
Barbara Szmajke M.Sc., tel: +48 022 8412940
Teresa Brauer, tel: +48 022 8413651
Mariola Chłopecka, tel: +48 022 8514369
Elżbieta Famuła, tel: +48 022 8412940

The department consists of 3 teams

  • Planning of control activity of the Institute unit
  • Research Organization Unit
  • Main Secretary

Planning of control activity of the Institute unit

This unit activity includes:

  • Sending the in-coming letters to the appropriate departments of the Institute,
  • Planning and organizing of the market surveillance testing concerning medicinal products on Polish pharmaceutical market,
  • Collecting the data concerning the negative  tests results (those not complying with the specification),
  • Keeping the records of medicinal products which quality has been questioned or which have been claimed as having side or adverse effects,
  • Keeping the list of medicinal products and medical devices which have been tested in the Institute (computer database),
  • Preparing and attending the meetings of Medicinal Products Control Commission,
  • Essential analysis of medicinal products and medical devices quality,
  • Information concerning medicinal products which have been registered in Poland and are authorized to be on the market.

Research organization unit

This unit activity includes:

  • Technical organization of Scientific Council,
  • Organization of work of Scientific Council Qualification Commission,
  • Organization of annual research projects submitted in Ministry of Science and Information Society Technologies,
  • Organization of the procedure of awarding researchers of the Institute prizes for theirs achievements,
  • Organization of students training in the Institute.

Main secretary

This unit activity includes:

  • Receiving and distributing of arriving correspondence (letters, packages, samples of medicinal products and medical devices to be tested) to appropriate departments of the Institute,
  • Computer data base concerning samples tested in the Institute,
  • Sending correspondence out of the Institute.