Clinical Research Internship Programme

Professional Certification
In Pharmacovigilance

Pharmacovigilance is the process of identifying and responding to drug safety issues and has grown considerably as a discipline over the past 10 to 15 years. We know that, Medicines and vaccines have transformed the prevention and treatment of diseases. In addition to their benefits, medicinal products may also have side effects, some of which may be undesirable and / or unexpected. Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem.

The pharmacovigilance industry are essentially the same as those of regulatory agencies; that is to protect patients from unnecessary harm by identifying previously unrecognised drug hazards, elucidating pre-disposing factors, refuting false safety signals and quantifying risk in relation to benefit.
Professional Certification in Pharmacovigilance is blended (Online + Offline) program in pharmacovigilance provides you basic & advance knowledge in pharmacovigilance principles and operations. The program also provides training on pharmacovigilance systems, global safety standards, guidelines and regulations & hands on training related to pharmacovigilance. The training curriculum is fully designed by expert faculty and is appropriate for candidates who wish to enter the pharmacovigilance sector.

Investigations
Course Curriculum
Other benefits
  • Eligibility : B.Pharm / M. Pharm / Life science/ Medical graduates and post graduates
  • Duration : 6 Months ( 4 Months Theoretical + 2 Months Practical Internship )
  • Placement : 100% placement assistance
  • Introduction To Clinical Research
    • ICH GCP Guidelines
    • New Drug Development Process
    • Project Management
  • General Overview Of Pharmacoviglance
  • PV- Basic Principles Of PV And AE/ADR Reporting Systems
  • Global Pharmacoviglance Regulatory Requirements In Pharmacoviglance
  • Safety Data Management
  • Safety Data Reporting
  • General Overview Of GVP
  • Quality In Pharmacovigilance
  • Safety Signal Management
  • Drug Safety In Clinical Trials
  • Overview Of Safety Database And Forms Used In The Actual Scenario
  • Digital Notes
  • Industry Based Learning
  • Live Interactive Sessions
  • 100% Internship & Placement Assistance

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