Clin Infotech

Advance Pharmacovigilance Certification Course In Hyderabad

PV-Pro: Pharmacovigilance Training and Internship

Advance Pharmacovigilance Course With Placements.

Pharmacovigilance is one of the most in-depth and fascinating areas of pharmaceutical science. The billion-bone assiduity requires competent and trained clinical exploration experts. Pharmacovigilance professionals are in high demand, and Clinical Research organizations are continually on the lookout for employees with relevant experience. This broad and diverse expertise provides outstanding job stability and enhanced earnings.

Clin InfoTech's Pharmacovigilance Course in Hyderabad could help you advance your profession in as short as four months. Externships on ongoing projects provide competent workers with extensive experience and competence in Pharmacovigilance Modules such as Case Processing, MedDRA Coding, Aggregate Reports, Drug Safety Physician, QPPV, Risk Management Plan, Audit and Inspection Readiness, Signal Management. Clin Infotech provides great career opportunities for Pharma IT aspirants wishing to work in an innovative company. It's a fast expanding industry, and India has emerged as a critical hub for clinical research, with a large need for trained clinical research specialists in the medical assiduity.

Intensive Training and Internship

Get Trained With Experience.

Pharmacovigilance Internship @ Clin Infotech

Join our transformative Pharmacovigilance Internship program and immerse yourself in dynamic learning with real-time Projects daily online classes, and internships. Our training methodology is confined to both theoretical and real-time industry. Enhance your resume and make meaningful connections. Earn course completion certificates to validate your expertise and boost your Employability and Open doors to exciting career opportunities in top Health Care Companies with Excellent Salary Packages.

Advantages Internship Program

Clininfotech in Hyderabad offers an enriching experience that goes beyond the conventional learning environment. Our internship program is crafted to provide participants with a unique set of advantages, ensuring their growth and success in the field of clinical research.

At Clin Infotech, our internship program is not just a checkbox; it's a transformative experience that prepares you for the dynamic and ever-evolving field of clinical research. Get ready to roll up your sleeves, engage with real-world projects, and emerge not just certified but truly job-ready.

Hands-On Learning for Real-World Success

Embarking on your journey to becoming a certified clinical researcher involves more than just theory; it's about translating knowledge into practical skills. At Clin Infotech, we understand the essence of experiential learning. Our Internship Program is your gateway to hands-on experience On Argus Safety Database and MedDRA Coding.

Discover the myriad benefits of our internship program:

  • Exposure to Pharmacovigilance Work Process: Acquire expertise in Pharmacovigilance Case Processing on Softwares Argus Safety Data base, Triage, Duplicate Checking, Casuality assessment.
  • Industry Insights from Experts: Benefit from the guidance and insights of experienced professionals in the Pharmacovigilance field, providing valuable mentorship throughout the program.
  • Networking Opportunities: Connect with professionals, peers, and industry experts, expanding your professional network and fostering collaborations.
  • Resume Enrichment: The practical experiences gained during the internship contribute to enhancing your resume, making you stand out in the competitive job market.
  • Enhanced Employability: The skills and knowledge acquired through the internship significantly boost your employability, increasing your chances of securing diverse career opportunities.
  • Regulatory Affairs Exposure: Gain an understanding of regulatory affairs in clinical research, ensuring compliance with ethical considerations and industry standards.
  • Pharmacovigilance Course Exposure: We believe in the power of immersive learning, and that's why our internship program spans a meaningful two months.

Course Content for Pharmacovigilance Course

  • ICSR Case Processing – On Argus Safety Database
  • MedDRA Coding
  • Aggregate Reporting
  • Drug Safety Physician
  • Signal Dection

What is Pharmacovigilance?

Pharmacovigilance is the research and practice of identifying, evaluating, comprehending, and avoiding side effects or other issues with medications or vaccinations. All drugs and vaccines are subjected to lengthy clinical trials before they are licensed for use. It tries to further medical knowledge by doing direct research on candidates or by collecting and analyzing blood, cells, tissues, or other samples.

Scope of Pharmacovigilance

Clinical research, among other things, evaluates the effectiveness and safety of drugs, devices, and diagnostic equipment before they are placed on the market. Pharmacovigilance is the science and practices concerned with the detection, assessment, comprehension, and avoidance of adverse effects or other medicine/vaccine-related issues. Before they are approved for use, all medications and vaccines are subjected to rigorous testing for safety and efficacy in clinical trials.

Job Opportunities in Pharmacovigilance

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Drug Safety Associate Pharmacovigilance Officer
Pharmacovigilance Manager Medical Reviewer
Drug Safety Executive Safety Surveillance Associate
Quality Associate Drug Safety Analyst
Clinical Coder Medical Writer
Pharmacovigilance Associate MedDRA Coder
Pharmacovigilance Associate Pharmacovigilance Officer
Subject Matter Expert Aggregate Reporter

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Pharmacovigilance Placement Preparation Program

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The Clin Infotech Edge What Sets Us Apart in Hyderabad

Internship Excellence:

Our programs emphasize hands-on learning through internships, providing you with real-world experience that makes you job-ready.

Job-Ready Programs:

Our courses are meticulously designed to equip you with the skills and knowledge needed for immediate entry into the clinical research field.

Advanced-Level Certificates:

Gain certificates that go beyond basic qualifications, showcasing your advanced proficiency in clinical research.

Real-Time Experienced Training:

Learn from seasoned professionals with real-world industry experience, ensuring that you're well-prepared for the challenges of the clinical research landscape.

Placement Assistance:

We're committed to your success. Our programs include placement assistance, facilitating your entry into the workforce right after completion.

Clin Infotech's complete certification program provides rigorous clinical research training throughout the full clinical trial process, from start to finish. This Clinical Trial Management course ensures that students have a procedural and administrative awareness of the clinical trial process, as well as the ability to expand skills and knowledge.

Eligibility:

Minimum Eligibility Criteria For Application To The Course Would Be Either Of The Following:
Applicants are recommended to have one of the following life Science degrees: Bachelor’s, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / M.Tech (Biotechnology), B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) and all professionals working with Pharmaceutical companies, CROs and Hospital.

Certification:

Certificate will be provided for this Course on successful completion of Assignments & Projects.
Certificate would be awarded at the end of the program by Clin Infotech. A fast track weekend course will also be conducted for employees & aspirants of Clinical Research Industry.

Our Placement Companies :

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Enroll with Clininfotech for an enriching learning journey that propels you toward a fulfilling and prosperous career in the realm of clinical research.

For more information, please contact Clin Infotech at careers@clininfotech.com or 8374457387