Clinrm

QPPV Services

Our Services

Revolutionary pharmacovigilance and drug safety services at the intersection of medicine and technology

LPPV and (Deputy) EU QPPV Services

PV procedural document design/adaptation

Medical evaluation of Individual Case Safety Reports

Subject narrative preparation for clinical study reports

Post-marketing and clinical SAE triage

Support for audits and inspections

Review and coordination of safety reports (PSURs, DSURs, RMPs, etc.)

Patient exposure calculation from shipment/IMS data

Global and local literature reviews

Study document review (protocols, CSR)

Representation in interdepartmental safety meetings

Query and data extraction from safety databases

Signal detection and risk management activities

Our commitment to drug safety is unwavering, ensuring that every pharmaceutical product meets the highest standards of quality and patient protection.

— PharmaVigilance Team

Specialty Solutions

Additional specialized services to support your pharmaceutical needs

Drug Safety & Pharmacovigilance

Investor reports & due diligence services

Literature Reviews

Medical affairs support and KOL development & engagement

Literature Reviews

Clinical trial recruitment strategies

Literature Reviews

Epidemiology services

Investor Reports & Due Diligence

AI-powered investor reports 

Tailored to your needs with validated information and timely delivery

Information Validation

Specialized physicians network for pharmacovigilance support.

Access to a global network of specialized physicians for pharmacovigilance support, including rapid SUSAR review (within 48 hours) and optimized safety strategies

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