SHARED WORK. SHARED VISION.

1987Harrison Clinical Research (HCR) founded in Munich, Germany by Dr. Francisco Harrison

1999Added clinical services

2001Added medical monitoring, safety and regulatory services

2005Marvin and SynCapture® EDC launched and IVRS developed

2011Attained Rave Accredited Plus after achieving Rave Safety Gateway status

2013Synteract acquired HCR, combining operations to become SynteractHCR and introduced ICD+

201232 rescue studies since 2010 alone

2014Achieved milestone of working in more than 60 countries

Shared Work. Shared Vision.Our mission is to support the innovation and development of better therapies in healthcare. Our focus on patients’ safety and comfort impels us to establish ethical standards for everything we do.

SynteractHCR is a multinational clinical research organization, formed from the merger of Synteract with Harrison Clinical Research in 2013, which provides global, full-service clinical trial services. We have more than two decades of experience supporting biopharma companies in all phases of clinical development across multiple therapeutic areas. We customize programs that will deliver timely, high quality data to help you get to decision points faster, taking time and cost out of drug development.

We deliver trials internationally. SynteractHCR has run trials in more than 60 countries across the globe, offering our clients strong international and regional clinical trial support throughout the world. Our geographic footprint extends from North America to Europe, and has an emerging presence in South America. We have a diverse, talented team of clinical development professionals who will exceed your expectations.

We have the right people and broad-based expertise. With longstanding therapeutic experience and a depth of clinical trial knowledge, SynteractHCR has a proven track record of success in all phases of clinical research. Our experts can help you in making smarter decisions and more confident choices. Our high percentage of repeat and referral business is proof that we have earned client confidence and loyalty. We are here for you: any time, any level, anyone.

We work together. We collaborate with every client to offer you a tailored approach to fit your project needs. We know every project matters and each is unique. You can outsource an entire project or only what you need. We work with you on your drug development goals to ensure every aspect is planned for and done right, while driving efficiencies and cost-effectiveness.

What we say is what we do. At SynteractHCR we believe that maintaining honest, ethical practices and keeping promises are important; transparency is a critical component to our partnership. You will get to know your project manager and team members as an extension to your in-house team. Trust us to deliver high quality, yet personal service.

1995Synteract founded in Carlsbad, California with DM services and biostatistics

“At SynteractHCR, we know each project is unique. Our clinical development expertise will help you navigate today’s complex development process.”

– Wendel Barr, CEO

Our Services: Phases I-IV

Project ManagementClinical Operations Data ManagementIWRS

Medical Monitoring Medical & Regulatory AffairsMedical Writing

Biotech & Pharmaceutical Companies

SynteractHCR has a solid understanding of the clinical development process for emerging, mid-sized and large biopharma companies. Many team members worked in biopharma before joining us. That experience gives them a 360° perspective. We have rescued many studies that otherwise would not have made it to completion, but have not had any rescued from us. Our experts will help you keep your clinical trials on track and within budget.

Medical Device Trials

We know the resource challenges that many medical device companies face. Our business processes and expert staff help us be efficient and cost-effective, while providing a personal approach. Whether you need full scope global services or only one particular service offering like data management or monitoring, our team of experts is here to help.

Specialty Segments

We have broad experience guiding companies in drug, diagnostic and device trials for a wide range of therapeutic areas, including a notable emphasis in oncology, central nervous system, infectious disease, endocrinology, cardiovascular and respiratory. With extensive experience in nutritional medicine, we’ve conducted many trials in nutritional health and diet-related diseases.

Why SynteractHCR?

BiostatisticsSafety Functional Service Provision

Our Clients

We have managed over 3500 projects across all phases of clinical development, and have contributed to numerous product approvals. During our history, we have addressed the most demanding drug development challenges.

We have conducted clinical trials in six continents and in more than 60 countries, with deep experience running studies in the US and Europe.

Worldwide offices allow us to support your trials internationally and in your time zones. Our strong presence in the US covers San Diego, California, Research Triangle Park, North Carolina and several other major biopharmaceutical hubs.

Our longstanding personnel and high experience levels mean you work with specialized teams familiar with our processes and aware of our dedication to quality and responsiveness.

We can handle all aspects of your Phase I-IV clinical trials. Our “Shared Work. Shared Vision” approach ensures that you have a partner who will provide the complementary support and expertise you need to meet your project goals.

www.SynteractHCR.comGlobal Headquarters

5759 Fleet StreetCarlsbad, CA 92008

Tel: +1 760 268 8200

A full-service, international CRO