Clinical Pharmacovigilance Service

Are you exploring options to outsource pharmacovigilance safety management for your upcoming clinical trial involving medicinal products for human use? Ensuring comprehensive safety oversight is not just essential—it’s critical to the success of your trial.

At Labmark, 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 an investigational drug’s safety profile.
Identify appropriate dosage levels.
Balance the risk/benefit ratio.
Detect potential risks and interactions.

To meet global and local regulatory requirements (e.g., Regulation EU No 536/2014 or Directive 2001/20/EC), guidelines (e.g., ICH-E6, ICH-E2B, ICH-E2F etc.), clinical trials require precise, traceable, and compliant safety management.

Why is it important?

Why is clinical pharmacovigilance important?

Participant safety

Protecting human participants is a top priority. Timely detection and management of adverse reactions or side effects ensure participant safety.

Data integrity

Compliance with ALCOA(+) principles ensures data quality, enabling smooth trial progression and eventual marketing authorization.

Regulatory compliance

Strict safety monitoring compliance avoids delays and regulatory issues, keeping your trial on track.

Risk management

Early detection and assessment of potential risks allows proactive strategies to minimize harm and support trial success.

Ethical considerations

Safeguarding participant well-being is a core ethical obligation in clinical research, demonstrating your commitment to responsible trial conduct.

How can we help?

We ensure clinical trials are conducted with the highest standards of safety, prioritizing patient care and well-being every step of the way.

Our pharmacovigilance (PV) services include:

Protocol review: ensuring trial protocols align with Good Clinical Practice (GCP) guidelines.
Safety Data Exchange Agreement (SDEA): establishing clear roles, responsibilities, and workflows for all parties involved.
Safety database management: setting up and managing E2B-compliant safety databases, including reconciliations.
Training: providing tailored pharmacovigilance training for sponsor and site staff.
Safety case evaluation, management, and expedited reporting.
Development Safety Update Reports (DSURs)

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Why labmark?

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

Expertise you can trust
With a team of highly skilled professionals boasting extensive experience, we ensure the utmost quality and safety for our clients.
24/7 accessibility
We ensure that our clients receive prompt assistance and support whenever they require it.