APCER life sciences

Silver Sponsor

Information

APCER Life Sciences provides comprehensive drug safety, pharmacovigilance, medical information, medical writing, regulatory services, quality assurance and risk management programs to pharmaceutical and biotech companies globally.

Our clients benefit from our vast experience in regulatory submissions across 100+ countries, consultative approach towards audit /inspection readiness and scientific support towards various therapeutic areas.

Our focus towards Patient Safety and Risk Profile Management makes us the preferred choice for pharma companies who are looking for pre /post marketing compliance & reporting solutions.

APCER’s customers are pharma and biotech companies who develop and commercialize products including biologics, vaccines, devices, consumer healthcare, combination products and cell & gene therapies.



Exhibitor Profiles
ConsultancyContact Research OrganisationDigital TransformationMedical DevicesPharmaceuticalPharmacovigiliancePV OutsourcingQuality Assurance & ComplianceRisk ManagementSignal Detection

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Contact details

+1 609 455 1600
marketing@apcerls.com
www.apcerls.com

Products & Services

Documents & Links

Pharmacovigilance Services in the European UnionLearn more about how we support the Biopharma companies in managing their pharmacovigilance and drug safety activities right from the clinical phases of trials
APCER FactsheetSnapshot of end-to-end Safety services offered by APCER Life Sciences. We provide comprehensive drug safety/pharmacovigilance, medical information, medical writ
Medical Information ServicesAPCER Life Sciences provides 24×7 fully customizable, multi-channel and multi-lingual Medical Information services to biopharma companies.
Risk Management ServicesWe offer comprehensive support in all aspects of risk management, including implementation, tracking, assessment, and modification of risk-management
Enabling global expansion by establishing an integrated PV systemAPCER helped a global pharmaceutical company in establishing a collaborative global pharmacovigilance (PV) governance model; setting up a single safety database
Enabling compliance through strong PSMF management & QPPV oversightOur team of experts enabled the company to address their inspection findings and helped streamline the processes to avoid any future deviations.
Leveraging Aggregate Reporting for EU-MDR ComplianceDiscover how we helped the company establish a robust process for preparing and delivering complex, high-volume reports in a timely and compliance manner.

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