IPHARMA provides full cycle of clinical development from early phase trials to registration and post-marketing PV.


 IPHARMA conducts various professional trainings and seminars in the framework of joint educational programs with specialized universities for personnel involved in the organization and conduct of clinical trials:


  • Pharmaceutical companies

  • Investigator site

  • Graduates preparing to work in the field of clinical trials

In 2016 IPHARMA signed scientific cooperation agreement with the I.M.Sechenov First Moscow State Medical University in which specialists of the company participate in educational and research projects making educational materials and more.

Our staff has developed special training programs for students with different levels of preparation that help get the necessary knowledge for the proper and effective work in clinical trials.

In addition to the theoretical discussion of the material obligatory part of each training is practical exercises that help a more efficient absorption of the material. Moreover, upon completing of each training, testing in accordance with educational program is done and the certificate is issued. 

​Trainings are conducted by employees with many years of experience in international and local clinical studies, including professional background as trainers.

  • GCP training/ GCP refresh training

  • Effective co-monitoring visit 

  • Monitoring Essentials training 

  • Phase I and bioequivalence studies 

  • Presentation skills

  • Audit findings and CAPA completion

  • SV Report and FU letter preparation

  • Introduction to oncology clinical trials 

  • Protocol development and writing 

For the staff of pharmaceutical companies and clinical sites, we offer a 1-2 day basics of Good Clinical Practice (ICH-GCP), pharmacovigilance trainings and training of especially the first phase of research at our office or at the customer's office. The format of the training and features can be agreed with the customer.

Since 2014 IPHARMA introduced and successfully implemented a program of the practical training of highly qualified personnel for the clinical trials industry, specialty "Clinical Research Associate". Internships within 1 month provides modular session in the training format, the seminars on the basics of monitoring at IPHARMA office combined with practical work in Investigator Sites.