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Welcome To

Pearl Pharmacovigilance Training Institute

We guide Science Graduates in beginning a new career path in pharma and corporate industry with experienced and trained professionals seeking to expand knowledge and skills

Courses Offered by PPVI

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Clinical research

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Medical coding and writing

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Pharmacovigilance

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Regulatory Device (Drug and Device)

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Medical device Management

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Pharmaceutical Quality Auditor

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+91 988 470 0344

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PPVI Focus

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Knowing the individual

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Setting up the course map for the individual

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Valued learning curve

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Growing up the individual standard

Unique Flavors of PPVI

FAQ's

Pharmacovigilance – A science with activities related to the detection, assessment, understanding and prevention of adverse effects or any other medicine/vaccine related problem.

No, as it involves a different array of pharmaceutical products like medical devices, biologicals, vaccines, traditional, herbal therapies, and cosmetic products. So, pharmacovigilance is applicable for all of these

Two types. 1. Active PV and 2.Passive PV
Active PV: Active (or proactive) safety surveillance means that active measures are taken to detect adverse events.

Passive PV: Passive surveillance means that no active measures are taken to look for adverse effects where voluntary reporting is made by health professionals and others to report safety concerns.

A ‘signal’ consists of reported information on a possible causal relationship between an adverse event and a drug, the relationship being unknown or incompletely documented previously. Usually, more than a single report is required to generate a signal, depending upon the seriousness of the event and the quality of the information

SUSAR is Suspected Unexpected Serious Adverse reaction. Serious adverse drug reaction (SAR) that is unexpected (per the product labels such as USPI, SPC etc.) or for which the development is uncommon (unexpected issue) observed during a clinical trial and for which there is a relationship with the experimental drug, whatever the tested drug or its comparator.

Regulatory Affairs is responsible for designing, implementing, and supervising regulations and guidelines to ensure that drugs meet safety and quality standards

Adverse Event (AE): In the context of pharmacovigilance and outside a clinical trial: any untoward medical occurrence in a patient to whom a medicinal product is administered and which does not necessarily have a causal relationship with this treatment (based on ICH-E2D Guideline, see GVP Annex IV).
An Adverse Drug Event (ADE) is “Harm caused by appropriate or inappropriate use of a drug whereas adverse drug reactions are a subset of these events, where harm is directly caused by a drug under appropriate use (i.e. at normal doses)

The Council for International Organisations of Medical Sciences (CIOMS), was founded by the World Health Organisation (WHO) and United Nations Education, Scientific and Cultural Organisation (UNESCO) in 1949.

Course Pricing Plan

Online
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40,000Total Package
  • Examination fee ₹1500
  • Flexible Learning
  • Live Webinars
  • 24/7 Support
Regular
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30,000Total Package
  • Examination fee ₹1500
  • In-Person Instruction
  • Hands-On Training
  • Comprehensive Materials
Network

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25,000Total Package

Network- applicable only when joined more than 5 people together

  • Examination fee ₹1500
  • Hybrid Learning
  • Expert Mentorship
Testimonial

What Our Students Says

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“Choosing Pearl Pharmacovigilance Training Institute was one of the best decisions of my career. The experienced professionals provided me with invaluable knowledge and practical skills that have been crucial in my current role in the pharmaceutical industry. The comprehensive training and personalized guidance truly set this institute apart.”

Aarti M
Science Graduate
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“The training at Pearl Pharmacovigilance Training Institute exceeded my expectations. The courses were thorough and the instructors were incredibly knowledgeable. They not only taught the material but also shared real-world experiences that helped me understand the industry better.”

Rajesh D
Pharma Industry Professional
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“Pearl Pharmacovigilance Training Institute offers exceptional training programs. The support from the staff and the quality of the curriculum were outstanding. They provided me with the tools I needed to transition smoothly into a corporate role. I highly recommend this institute to any science graduate looking to enter the pharma sector.”

Neha R
Corporate Trainee
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“The training I received at Pearl Pharmacovigilance Training Institute was transformative. The blend of theoretical knowledge and practical application prepared me well for the challenges of the pharmaceutical industry. The career support services were also invaluable in helping me secure my first job.”

Vikram T
Pharmaceutical Analyst