Integrated Pharmaceutical Services Across APAC

Flexible services designed around your countries, products, timelines and operating model.

iPharmX Pte Ltd is a Singapore-based pharmaceutical services company supporting pharmaceutical, biotechnology and healthcare organisations across Asia-Pacific.

Our experienced professionals provide quality-managed support in Pharmacovigilance, Medical Information, Clinical Operations, Clinical Data Management and Regulatory Compliance.

We work with clients through project-based assignments, ongoing retained services and regional coordination models. Each engagement is structured to support compliance, clear oversight, inspection readiness and efficient delivery.

Discuss Your Requirements
iPharmX pharmaceutical services and regulatory support

Our Core Services

Specialised support across the pharmaceutical product and clinical development lifecycle

Pharmacovigilance

End-to-end drug safety support for clinical trials and marketed products, helping clients protect patients and meet local and global requirements.

  • Local safety contact and LPPV support
  • ICSR and expedited safety reporting
  • Literature and regulatory intelligence monitoring
  • Aggregate reports and risk management support
  • Audit and inspection readiness
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Medical Information

Accurate, consistent and compliant management of medical enquiries from healthcare professionals, patients and business partners.

  • Medical enquiry intake and coordination
  • Product and scientific information support
  • Adverse event and complaint identification
  • Medical response content development
  • Documentation and quality review
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Clinical Operations

Operational support for clinical studies with a focus on quality, coordination, documentation and regulatory compliance.

  • Clinical trial coordination support
  • Study documentation and tracking
  • Site and vendor coordination
  • Safety submission support
  • Inspection-ready study documentation
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Clinical Data Management

Clinical data management support designed to strengthen data integrity, traceability, quality and database readiness.

  • Data management planning
  • Database and eCRF support
  • Data review and query management
  • Reconciliation and quality control
  • Database lock readiness
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Regulatory Compliance

Practical regulatory support throughout the product lifecycle, aligned with applicable local and regional requirements.

  • Regulatory intelligence and gap assessment
  • Submission planning and coordination
  • Local regulatory support
  • Compliance documentation and maintenance
  • Post-approval lifecycle support
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Why Partner With iPharmX?

Regional expertise supported by structured quality processes

Asia-Pacific Expertise

Practical understanding of local regulatory processes, safety reporting requirements and regional operating expectations.

Experienced Professionals

A dedicated team with pharmaceutical, CRO, clinical research, pharmacovigilance and regulatory experience.

ISO 9001:2015 Certified QMS

Controlled processes, documented oversight and consistent service delivery supported by a certified Quality Management System.

Flexible Engagement Models

Support structured around your operational requirements

Project-Based Support

Defined deliverables, timelines and responsibilities for targeted assignments.

Ongoing Retained Services

Continuous operational support for recurring local or regional responsibilities.

Regional Coordination

Central coordination across multiple APAC countries, partners and stakeholders.

Looking for Pharmaceutical Support Across APAC?

Share your scope, countries and timelines with us. Our team will review your requirements and recommend an appropriate support model.