Our offer of expert services includes:

  • evaluation of the documentation of active substance manufacturers (ASMF, DMF, CEP)
  • development of task and time schedules for research and development work
  • development of reports on completed research and development stages
  • preparation of literature and patent studies
  • development of full analytical and technological documentation regarding product development, including documentation in CTD format, necessary in the registration process of medicinal products, in accordance with applicable guidelines and legal acts
  • development of specifications for starting materials and final products
  • conducting training and workshops for researchers and members of research teams regarding the organisation and conduct of clinical trials, as well as the principles of good clinical practice (GCP)