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  • Training “Quality control in the system of quality assurance of drugs. Introducing the concept. Basics of local and international law. Aspects of practical application and quality assurance of medicines in non-production organizations of the pharmaceutical industry. Responsible for ensuring the quality of drugs in the non-production organization "
  • Training "The rules of good manufacturing practice (GMP). Introducing the concept. Basics of local and international law. Aspects of practical application of the principles of GMP in non-production organizations of the pharmaceutical industry."
  • Training "Regulatory Manager"
  • Training "Regulatory Specialist" (specialist for registration)
  • Basic Training "Clinical trials of medicines, GCP rules"
  • Training "Specialist in Pharmacovigilance"
  • Training "Clinical trials of pharmaceutical products. GCP. Standard business process.Practical aspects of clinical trials organization, management and closing. "
  • Training "Pharmacoeconomic studies of pharmaceutical products"
  • Post-marketing studies of drugs
  • Training-session – upon your wish, interest in field of our competence.

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