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    Clinical Pharmacovigilance Service – Comprehensive safety oversight for your clinical trials

    Clinical Pharmacovigilance Service

    Comprehensive safety oversight for your clinical trials

    Pharmacovigilance is the science of detecting, assessing, and preventing adverse effects. At QbD Group, we offer full pharmacovigilance services for the safety management of your clinical trials.

    What is clinical pharmacovigilance?

    Pharmacovigilance is the science of detecting, assessing, and preventing adverse effects or drug-related problems during clinical trials.

    High-quality safety data is essential to determine safety profiles, identify dosage levels, and balance risk/benefit ratios. To meet global and local regulatory requirements (e.g., Regulation EU No 536/2014, ICH-E6), clinical trials require precise, traceable, and compliant safety management.

    Clinical Pharmacovigilance

    Why is clinical pharmacovigilance important?

    Protecting participants and ensuring compliance are top priorities in clinical research.

    Participant safety

    Timely detection and management of adverse reactions ensure participant safety.

    Data integrity

    Compliance with ALCOA(+) principles ensures data quality for smooth trial progression.

    Regulatory compliance

    Strict safety monitoring avoids delays and regulatory issues.

    Risk management

    Early detection allows proactive strategies to minimize harm.

    Ethical considerations

    Safeguarding participant well-being is a core ethical obligation.

    How can we help?

    We ensure clinical trials are conducted with the highest standards of safety, prioritizing patient care.

    Protocol review

    Ensuring trial protocols align with GCP guidelines.

    EudraVigilance registration

    Assisting with setup and maintenance of the EudraVigilance database.

    SDEA

    Establishing Safety Data Exchange Agreements.

    Safety database management

    Setting up and managing E2B-compliant safety databases.

    Training

    Tailored pharmacovigilance training for sponsor and site staff.

    Safety case management

    Evaluation, management, and expedited reporting of safety cases.

    DSURs

    Creation of Development Safety Update Reports.

    PV Process
    QbD Group expertise

    为什么选择QbD Group

    您值得信赖的合作伙伴

    Do you lack an in-house safety team, or just need expert guidance? QbD Group is here to help.

    Expertise you can trust: highly skilled professionals ensuring utmost quality and safety.

    24/7 accessibility: prompt assistance and support whenever required.

    规划您的临床路径

    从差距评估到完整 CRO 交付,我们的临床专家随时为您的 MedTech 旅程提供支持。

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