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Pharmacovigilance

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Safety is an essential ingredient of any clinical studies. Pharmacovigilance is like a sunshade to represent activity for continuous monitoring and evaluating side effects related with medicines.

It is a key component of effective drug regulation systems, public health programmes and clinical practice.

A step closer towards Drug Safety

We believe in continuous regulatory compliance through procedure excellence and an reliable assurance to Quality.

We offer inclusive associate pharmacovigilance consulting services transversely globe to our valued clients from Case Intake to Safety Risk Management through regulatory compliance, higher efficiency and deliberate drug safety consequences.

We leverage our field knowledge and widespread industrial knowledge to provide “One-stop” Pharmacovigilance facilities:

1. Experienced team: Team covers vastly knowledgeable safety and regulatory professionals as well as medical experts across the globe, involved in providing high-quality PV, regulatory, and QPPV facilities to our industry-leading clients.

2. Commitment: In order to ensure on-time, efficient implementation, our global safety team coordinates efforts with market-leading clients, identifying and anticipating their pharmacovigilance needs.

3. Experts: A wide-ranging global network of partners and key opinion leaders is one of our key assets. Our expert teams in operations, technology, and access support the entire pharmacovigilance journey, from proof-of-concept to end-to-end services.

4. Quality and goal: We have successfully passed inspections by various Regulatory bodies without any observations, a testament to our experience, knowledge, commitment, and excellence in serving our clients globally by providing benchmark-level services.

5. Multiple Capabilities: Demonstrated capability to handle high case volumes and adapt to volume fluctuations.

Adverse Event Reporting: Adverse event (AE) reporting involves the receipt, triage, data entry, assessment, distribution, reporting (if appropriate), and archiving of AE data and documentation.

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