- Pharmacovigilance
Safety Management

We maintain a close check on your project to ensure that all the requirements are met.

Safety Management

Pharmacovigilance, also known as drug safety, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. It is practice of monitoring the safety and effectiveness of medicinal products after they have been authorized for use. It involves collecting and analysing data from various sources, including healthcare professionals, patients, and regulatory authorities, to identify and evaluate potential safety issues associated with a medicine.
Pharmaceutical Industries focus to upsurge their market globally to maximize profit in a shorter possible timespan. Most of the companies have achieved this by outsourcing Pharmacovigilance services.
Our Pharmacovigilance services, supported by our in-depth knowledge of drug development process helps to improve client’s profitability by supporting various Pharmacovigilance related services using latest data base from Glob.

Complying with regulations and ensuring product safety.

Whether you are a small biotech or a large pharmaceutical company, IQVAMED has the expertise to help you succeed in today’s challenging healthcare environment. We are committed to providing our clients with the highest level of service and support, and we are dedicated to helping them improve compliance and product safety through innovative approaches and expertise.

In Scope of End-to-End Safety Solutions

Pharmacovigilance Operations

Expedite Reporting

Aggregate Reporting

Signal Detection and Risk Management

🙶 A Survey to Evaluate Healthcare Professionals' Awareness, Knowledge, and Reporting Methods of Adverse Drug Reactions (ADRs) and Serious Adverse Events (SAEs): An Assessment of Current Practices and Opportunities for Improvement. 🙷

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Our Expertise and qualified person for pharmacovigilance (QPPV’s) are able to :

Appropriate Measures to Collect and Collate All Reports SADRs :

We take appropriate measures to collect and collate all reports of suspected adverse reactions associated with medicinal products for human use originating from unsolicited or solicited sources. And our system allow the acquisition of sufficient information for the scientific evaluation of those reports.

Our Designed and structured system help to ensure that the collected reports are authentic, legible, accurate, consistent, verifiable and as complete as possible for their clinical assessment, and allows for reports of suspected adverse reactions to be validated in a timely manner and exchanged between competent authorities and IQVAMED within the legal submission time frame.

Safety Data Monitor

IQVAMED monitor pharmacovigilance data to determine whether there are new risks or whether risks have changed or whether there are changes to the risk-benefit balance of medicinal products and update the risk management system and the RMP.

We offer a comprehensive range of risk management services to ensure that our clients’ products are developed, monitored, and marketed safely and effectively.

RMP Development

Our experienced risk management team works closely with clients to develop customized Risk Management Plans (RMPs) that identify potential risks, evaluate risk factors, and create strategies to minimize risks. We follow a rigorous process that includes thorough analysis of safety data and compliance with regulatory requirements.

RMP Quality Management

We have a robust quality management system for risk management that ensures compliance with regulatory guidelines and adherence to best practices. Our team of experts is committed to ensuring that all safety data is collected, analyzed, and reported with the utmost accuracy and integrity.


Review the existing Pharmacovigilance systems and establish its compliance with Regulation:

IQVAMED offers a full range of Pharmacovigilance audit services in accordance with good pharmacovigilance practices (GVP) requirements and global regulations.

In addition to our standard comprehensive system GVP auditing services, IQVAMED offers a flexible and customizable GVP auditing service that can cover one or multiple sectors on a global scale. Our team of experienced pharmacovigilance professionals can tailor our auditing services to meet the specific needs of our clients in the pharmaceutical, biotech, and medical device industries.

At IQVAMED, we are committed to providing our clients with the highest quality of service, and our customized GVP auditing service is designed to meet the unique needs of each client. Our global reach and expertise allow us to provide comprehensive auditing services that meet regulatory requirements and ensure the safety and well-being of patients.

Pv System and Process Audits