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Clinical Trial Management in the US: Local Service, Global Reach

SGS delivers clinical trials with high-quality data across the Americas and Europe. Our comprehensive clinical trial management services offer you tailored solutions and global coverage with local knowledge.

SGS helps you bring new therapies to market safely and quickly through experienced staff, efficient and accurate feasibility and optimized start-up timelines – with a flexible, customer-focused approach.

With over 40 years of experience as a full-service contract research organization, we provide a wide range of integrated services across the USA – from drug development consultancy activities to Phase I-IV trial management, as well as bioanalytical and QC testing. We offer unrivaled expertise in international project management and clinical monitoring, and we operate a global network of therapeutic-specific key opinion leaders, subject-matter experts and pre-qualified investigator trial sites. We also provide regulatory guidance and regulatory IND/NDA submission experience in the USA, Canada and Europe, along with expertise in drug import regulations and procedures for every country in Europe and North America.

Contact us to learn more about our clinical trial management solutions:

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Medical Writing

Biometrics

Pharmacovigilance and Drug Safety Services

Regulatory Affairs

Clinical Pharmacology Unit

Laboratory Services

Clinical Trial Management (Phase I-IV)

Clinical Study Feasibility Services

SGS Clinical Trial Management

Our flexible clinical trial management solution provides you with:

Strategic, data-driven feasibility which allows fast, easy access to patient groups
A robust and systematic approach to clinical site evaluation and selection, using local feasibility experts
An extensive global network of therapeutic-specific key opinion leaders, subject-matter experts and pre-qualified investigator trial sites
Experienced customer-focused project managers, based across Europe and North America
Comprehensive site management and quality-focused clinical monitoring
An international network of highly qualified and trained local CRAs
Medical monitoring and pharmacovigilance
Regulatory guidance and a dedicated team of regulatory affairs experts in place for 70 countries, including the US
Integrated CTMS and eTMF on an industry-leading platform
Integrated data cleaning, analysis and reporting in collaboration with our biometrics team
Medical and regulatory advice for clinical development plans and study protocol designs