Safety first, at every step
Pharmacovigilance
At TELOS-C, our pharmacovigilance expertise is built on a dual, complementary approach:
ensuring regulatory compliance while adapting to the specific needs of each organization.
We support safety data management during both clinical trials and post-marketing phases, with a focus on coding accuracy, data harmonization, and regulatory alignment.
Precise coding, consistent systems
Medical Coding for Safety Data
Medical Coding
for Safety Data
Our team codes Serious Adverse Events (SAEs) using MedDRA and other standard dictionaries.
We perform SAE reconciliation to ensure consistency between clinical and pharmacovigilance databases—reducing discrepancies and improving the evaluation of safety signals.
Reliable compliance, full coverage
Our Pharmacovigilance Services Include :
Provision of EU QPPV and Local Contact Person (Belgium)
Management of CIOMS forms, literature reviews, and safety reports (PSUR, DSUR, RMP)
Drafting and maintenance of SOPs for PV activities
Tailored training sessions for medical and regulatory teams
Provision of EU QPPV and Local Contact Person (Belgium)
Management of CIOMS forms, literature reviews, and safety reports (PSUR, DSUR, RMP)
Drafting and maintenance of SOPs for PV activities
Tailored training sessions for medical and regulatory teams
Tailored support for all structures
Flexible & Scalable Support
Whether complementing large in-house PV departments or fully managing safety for smaller organizations, our solutions adapt to your structure.
Regulations are the same for all—but your constraints aren’t. That’s why our model combines compliance with adaptability and efficiency.
Two decades of trusted vigilance
20+ Years of Expertise
With over 20 years of experience in pharmacovigilance, TELOS-C provides reliable, responsive, and compliant support.
We help you ensure data quality, regulatory readiness, and above all, patient safety—every step of the way.