Our Services

Landmark Research provides our partners with a full range of clinical services, from start-up to close-out and everything in-between.

Medical Writing Service

Our team is highly experienced in producing high-quality documents such as clinical study protocols, investigator brochures, and regulatory submission documents. We use the latest software and technologies to ensure accuracy and timeliness. Our services are offered at competitive rates…

Biostatistics Service

Our team’s in-depth understanding of regulatory and clinical requirements allows us to apply strict statistical and research principles for the design, execution, and analysis of your clinical trial…

Regulatory Service

At Landmark Research, we take immense pride in our unrivaled regulatory services as a leading Contract Research Organization (CRO). With years of experience and a team of accomplished regulatory experts, we offer a comprehensive suite of solutions for pharmaceutical products and medical devices throughout the regulatory journey…

Pharmacovigilance

Our steadfast commitment to patient safety and product quality drives our comprehensive pharmacovigilance services. With a team of skilled professionals, we monitor and assess adverse events and potential risks associated with pharmaceutical products and medical devices throughout their lifecycle…

Clinical Operations

The primary objective of Landmark Research is to maintain consistent adherence to high-quality standards in clinical trial conduct and ensure exceptional delivery of study outcomes. Our overarching goal is to provide indispensable and pragmatic solutions throughout every stage of a clinical trial, including project planning, trial initiation, study execution, and study completion…

Clinical Data Management

Clinical data management services encompass a range of activities and processes involved in the collection, cleaning, validation, and maintenance of clinical trial data…