Providing end-to-end pharmaceutical and healthcare consulting services that address regulatory, operational, & clinical needs.
With deep roots in both public and private healthcare sectors, our team supports life sciences companies, hospitals, research organizations, and government agencies in achieving their goals with precision and compliance. From market access and drug safety to medical writing and clinical development, our solutions are powered by licensed professionals and guided by industry standards.
Comprehensive Care, Compliance, and Capability
Regulatory Affairs
We help clients navigate the complex regulatory landscape governing pharmaceuticals and healthcare products by providing expert guidance in regulatory strategy, dossier preparation, labeling compliance, and submission support. Our team ensures that every interaction with health authorities - including the FDA, EMA, and other global agencies - is timely, compliant, and effective. We also prepare clients for inspections and audits, ensuring pre-approval readiness at every stage.
Pharmacovigilance & Drug Safety
Patient safety is at the heart of our drug safety services. Our pharmacovigilance team manages adverse event reporting, conducts signal detection analysis, and develops comprehensive risk management plans. We oversee literature monitoring and ensure all compliance documentation is accurate and audit-ready. From setting up global pharmacovigilance systems to training clinical and commercial teams, we help our clients maintain safety standards across the product lifecycle.
GMP Compliance & Quality Assurance
We deliver GMP and GxP compliance solutions that uphold the highest industry standards for pharmaceutical quality. Our services include conducting internal audits, guiding inspection readiness, managing quality control testing, and drafting documentation that supports regulatory expectations. We also implement and monitor CAPA plans and support manufacturing process validation through the development of robust SOPs and process controls.
Drug Development & Clinical Support
Our drug development services span from early-phase clinical trial design to final regulatory submissions. We assist with protocol development, biostatistical analysis, and data management while ensuring full compliance with regulatory requirements. Our support extends to investigator engagement, feasibility studies, and the overall coordination of clinical projects, enabling efficient and compliant advancement through the research pipeline.
Market Access & Pharmaceutical Distribution
With a licensed distribution network and deep knowledge of pharmaceutical logistics, we enable product access and regulatory alignment in competitive markets. Our services include pricing strategy, reimbursement consulting, inventory control, and cold chain logistics management. We also support government procurement programs and provide end-to-end solutions for distributing both prescription and over-the-counter medications across public and private sectors.
Medical Writing & Communications
Our medical writing team specializes in translating complex clinical data into clear, compliant, and scientifically sound communications. We produce regulatory documents such as CTD modules and safety narratives, prepare manuscripts for publication, and develop educational materials like product monographs and training guides. Whether supporting a regulatory filing or communicating findings to stakeholders, we ensure accuracy, clarity, and alignment with medical standards.
Industry Alignment & Compliance
Marpconsulting upholds the highest standards of quality and ethics across all pharmaceutical operations. Our services are fully compliant with global and national regulatory frameworks, including WHO and FDA Good Manufacturing Practices (GMP), ICH guidelines, Good Pharmacovigilance Practices (GVP), ISO quality systems, and local drug regulatory authority requirements. This ensures that every solution we deliver – from development to distribution – meets rigorous safety, efficacy, and accountability.
Our pharma capabilities are driven by three specialized brands:
- MarpPharma, which focuses on regulatory affairs, quality assurance, and pharmaceutical distribution.
- MarpRx – pharmacovigilance, safety monitoring, clinical support.
MarpHealth – healthcare consulting, program design, and public health solutions.
Together, these divisions enable us to support a wide range of government and commercial health missions, including contracts with federal agencies, military healthcare systems, hospitals, and pharmaceutical manufacturers.