Services

Pharmacovigilance Services & Solutions

We are the pharmacovigilance experts who combine technology and expertise to make your drug safety monitoring faster, clearer, and more cost-efficient.

Comprehensive Pharmacovigilance Services Tailored to Your Needs

As a pharmacovigilance services supplier we can work in flexible formats offering full end-to-end drug safety services, retrospective searches, or targeted monitoring of individual areas such as literature or regulatory authorities updates.

End-to-End Pharmacovigilance Support

End-to-end pharmacovigilance support covers far more than a literature review. Our comprehensive pharmacovigilance solutions include structured case intake and triage, standardized case processing, medically grounded causality assessment, and clear, compliant narrative creation ensuring all safety data is evaluated consistently, documented accurately, and ready for timely regulatory submission.

Retrospective Searches

Retrospective medical review helps recover historical drug safety and pharmacovigilance data by reviewing past literature, regulatory updates, and reference sources. Such drug safety services ensure patient safety so no relevant information is missed and your pharmacovigilance documentation is complete and accurate which supports audits and inspections, and strengthens the completeness and accuracy of your pharmacovigilance documentation.

Focused Scalable Solutions for Pharma

Our pharmacovigilance team can focus on a single stream (literature or regulatory updates, reference products monitoring). This model delivers precise, relevant insights without unnecessary scope, ensuring compliance while keeping your pharmacovigilance workload efficient and manageable.

Ensure Compliance with Us

Projects Successfully managed by our pharmacovigilance team

2209

Products Monitored across multiple markets

Countries Monitored by
our team

Full Set of Pharmacovigilance Solutions for Different Business Types

Our PV team understands the real post-marketing and pharmacovigilance needs of MAHs and CROs and provides reliable, high-quality services tailored to your workflows. Our specialists actively support 14 projects across multiple countries, giving us hands-on experience with local regulatory requirements and compliance expectations.

Our Core Pharmacovigilance Service Offerings

Our team offers a full suite of post-marketing surveillance that includes global and local literature monitoring, signal management, safety reporting, risk evaluation, quality control, and development safety update reports.

Local and Global Literature Screening & Monitoring

Our pharmacovigilance professionals provide reliable global literature monitoring through PubMed. We also cover local literature across 108 countries, ensuring compliant, consistent literature surveillance aligned with regional pharmacovigilance requirements.

Case Processing & Individual Case Safety Reports (ICSRs)

Our experienced team helps customers manage the full cycle of drug safety cases (collection, processing, assessment, submission, and follow-up) across both local and global markets, ensuring reliable and fully compliant case handling.

Local Safety Officer (Local QPPVs)

We provide qualified Local QPPVs for seamless interaction with local authorities, delivered through our internal team or an established network of affiliate experts worldwide.

Signal Detection

We support effective signal detection by helping you collect, manage, and interpret large volumes of drug safety data to identify potential risks early.

Regulatory Intelligence

We provide structured tracking of official websites (competent regulatory authorities, health authorities), ensuring timely updates on safety requirements, guidance changes, and emerging regulatory expectations.

Reference Products Monitoring

Our pharmacovigilance services include reference product monitoring to track safety risks and quality information for innovator medicines and their generics.

Medical Writing

We provide medical writing services to create clear, compliant safety documentation including narratives, reports, and regulatory materials.

Periodic Safety Documentation Management (PSUR, DSUR, Risk Management plans)

We manage periodic safety update reports, development safety update reports, risk management plans, support updates to SOPs, PSMFs, and SDEAs through our scientific, local, and quality assurance experts.

Pharmacovigilance Training & Consultancy

Our trainers with over a decade of educational extensive experience and PhD-level expertise guide your team through current PV standards and best practices.

Why Choose DrugCard as a Pharmacovigilance Service Provider

Proprietary PV Technology – our in-house platform streamlines monitoring, reduces manual workload, and increases operational efficiency.
AI-Enhanced Article Evaluation – automated assistance speeds up literature assessment while improving consistency and accuracy.
Integrated Data Workflows – literature insights link directly to our safety database, enabling automatic pre-filling of key fields.

DrugCard Is a Team of Experienced Pharmacovigilance and IT Experts

DrugCard’s founders bring over 10 years of experience in drug safety and pharmacovigilance, regulatory affairs, and software development. We ensure global coverage & regulatory compliance for patient safety.

How Our Pharmacovigilance Services Work

We deliver pharmacovigilance services through a structured, transparent process designed to ensure fast onboarding, consistent execution, and full visibility into safety activities.

1. Simple Onboarding Process

Projects start within two business days, with the first monitoring report delivered within one week. Where needed, we also support retrospective searches to ensure historical safety data is fully covered.

2. Dedicated Account & Project Management

Each project is managed by a dedicated team that aligns activities with your SOPs, oversees daily operations, and ensures smooth communication throughout the collaboration.

3. Transparent Reporting & KPIs

Clients receive access to activity logs, compliance KPIs, and performance metrics, providing full transparency into our pharmacovigilance processes.

Benefits of Outsourcing Pharmacovigilance Services

Cost-efficient – our proprietary monitoring platform automates routine PV tasks and reduces manual workload, allowing us to deliver high-quality services at a lower operational cost.

Transparent – clients receive direct access to reports, activity logs, and compliance KPIs, providing full visibility into ongoing pharmacovigilance activities aligned with their SOPs.

Flexible – both our platform configuration and team structure can be adapted to specific products, markets, reporting frequencies, and internal workflows.

Fast start – projects are onboarded within two business days, with the first monitoring results delivered within one week.

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