ACRI India

ACRI India Avigna Clinical Research Institute is modelled on the lines of some of the premier Clinical Research Institutes of India.

ACRI – Avigna Clinical Research Institute is a part of Avigna Learning Academy. ACRI – Clinical Research Institute is modeled on the lines of some of the premier Clinical Research Institutes of India. We are dedicated and committed to provide excellent Clinical Research Professionals to the Clinical Research Industries.

28/10/2025

Yellow card- Adverse event reporting system
The Yellow Card Scheme is a vital part of pharmacovigilance that allows healthcare professionals and the public to report any suspected side effects or problems with medicines and vaccines. Even small or unexpected reactions matter — because your report could help identify a new safety issue and prevent harm to others. It’s an easy way to be part of a safer healthcare system!

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22/10/2025

MedWatch: Adverse Event Reporting System
MedWatch is the U.S. FDA’s safety information and adverse event reporting program that allows healthcare professionals and consumers to voluntarily report problems with medical products, including drugs, biologics, medical devices, and dietary supplements. The goal is to detect early signs of product-related risks or side effects that might not have been seen during clinical trials.
By collecting and analyzing these reports, the FDA can take timely action—such as updating safety labels, issuing recalls, or releasing public alerts—to protect patients and ensure product safety.
In short: MedWatch is a vital link between real-world patient experiences and regulatory safety decisions.

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Vulnerable subjectsVulnerable subjects in clinical trials are individuals who may have limited capacity to make informed...
20/10/2025

Vulnerable subjects
Vulnerable subjects in clinical trials are individuals who may have limited capacity to make informed decisions about participation. Special protections are put in place to ensure their rights and safety are upheld, including the need for informed consent and careful ethical oversight during the trial process.
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Embark on a transformative career journey with ACRI' upskilling courses. Empower yourself with cutting-edge skills and k...
16/10/2025

Embark on a transformative career journey with ACRI' upskilling courses. Empower yourself with cutting-edge skills and knowledge to unlock new opportunities and propel your professional success. Elevate your career trajectory with targeted upskilling for a brighter, more fulfilling future.

🌐 Website: www.acriindia.com
📧Email : info@acriindia.com
📞 Call : +91 9741600499

15/10/2025

Job shift?
Changing jobs is difficult but it's good if you get the right job. Upskill with ACRI and make the right shift.

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Contact us: +91 9741600499

Ozempic the wonder drugOzempic has found its way as a weight loss drug in the office label market and has gained popular...
14/10/2025

Ozempic the wonder drug
Ozempic has found its way as a weight loss drug in the office label market and has gained popularity as the wonder drug. Many celebrities around the world have vouched for the benefits of this drug. Off late, the pharmaceutical market has noticed some adverse effects on taking the drug and Ozempic takers are cautious.

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Contact us: +91 9741600499

08/10/2025

What is SAE Reconciliation?
In clinical research, a Serious Adverse Event (SAE) reconciliation is the process of comparing and aligning the information about serious adverse events that appear in two different sources of data that is Clinical Database and Safety Database. Sometimes, the same SAE may be reported slightly differently in the two systems (e.g., missing dates, different terminology, or not updated). So SAE reconciliation ensures accuracy, both databases must match before the trial database is locked or before reporting to regulators.

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07/10/2025

CAREER IN TROUBLE?
Changing careers in today’s scenario is challenging. The market is dull and layoffs are plenty. Don't wait for someone to fire you. Upskill yourself with our job oriented courses and shift your career. Want to know more? Give us a ring.

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Contact us: +91 9741600499

01/10/2025

Who is a CRC?
CRC is a person who conducts the clinical trial. He/ she can be a life science or health science personal. All activities are managed by the CRC. He acts as a link between the PI and the research team.

🌐 Website: www.acriindia.com
📧Email: info@acriindia.com
Contact us: +91 9741600499

01/10/2025

✨ Happy Ayudha Pooja! ✨
May this festive occasion bless you with strength, success, and prosperity. Let’s celebrate the tools that empower us to create, innovate, and grow! 🌸🛠️

🌐 Website: www.acriindia.com
📧Email: info@acriindia.com
Contact us: +91 9741600499

30/09/2025

ACRI offers specialized courses in regulatory affairs, providing expert guidance to navigate complex landscapes and enhance compliance. For a successful career path in clinical research, upgrade your skills with ACRI.

🌐 Website: www.acriindia.com
📧Email : info@acriindia.com.
📞 Call : +91 9741600499

Address

Avigna Clinical Research Institute – ACRI No. 33, 4th Floor , 15 Th Cross, 2 Nd Phase, J. P. Nagar 100ft Ring Road
Bangalore
560078

Telephone

+919741600499

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