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Accelovance, Inc.



Catering to Sponsor Business Needs & Strategic Objectives

"BEST CRO" ViE Award Winner

2009 - 2010 - 2011

Industry Recognition for Excellence

Accelovance's award-winning, innovative and proven approaches have optimized clinical productivity and performance; delivering greater predictability, higher quality and performance assurances for those we serve. Additionally, we manage with financial responsibility, sensitivity to timelines, maximized efficiencies and unwavering focus on excellence. Client satisfaction, strong team relationships, quality data and a sense of partnership and collaboration are what define success for our organization.

Proactive Phase I-IV Study Management & Therapeutic Expertise

Our patient-centric study perspective means Accelovance thinks about the patient/study participant first and foremost. This analysis leads us to identify the best clinical sites who will deliver the highest quality data for the Sponsor. We hold ourselves accountable for delivering on commitments, supporting critical study milestones, meeting Sponsor quality standards and controlling study budgets. Accelovance has diverse therapeutic expertise including: vaccines, infectious diseases, immunology, metabolic, diabetes, dermatology, neurology, cardiovascular, men and women's health, gastrointestinal, nutraceutical, dietary supplements, consumer health products, healthy volunteer and safety studies.


- FLEXIBLE, Full-Service CRO

- Accelovance Owned/Operated Research Dedicated Clinical Sites

- Patient "Management" Solutions: Recruitment, Retention, Compliance

- CLINICAL Call Center

- Regulatory Support / IND Services

- International Reach: North America / Europe / Latin America / Emerging Markets / China

Accelovance's ownership and operation of clinical sites provides unique insight to operational efficiencies that position our CRO to have enhanced control over quality, enrollment, timelines, retention/compliance, and study budgets; even when working with non-Accelovance sites. We leverage the knowledge gained from operating several clinical service divisions to implement flexible, cost-effective solutions that meet Sponsor resource needs, study timelines and strategic objectives. Whether these services are utilized independent of one another or in an integrated manner to maximize efficiencies and control, Accelovance supports each study with commitment, relationship, responsiveness and passion.

CRO Services: flexible to meet your needs. Project Management, Regulatory Affairs, Quality Assurance, Medical Monitoring, Clinical Monitoring, Data Management, BioStatistics, IND & Regulatory Support, Safety and Late Stage Services. What service is needed to augment your internal clinical team? Or serve as a full-service outsourced study management solution? Accelovance offers these services as needed and is flexible to work with other preferred vendors. Our ownership of sites gives the CRO team the additional patient and operational perspective necessary to effectively manage the study and position any clinical site for success.

Clinical Sites: Accelovance owned and research dedicated. Our six (6) research clinics average 3,000 SF in size and are staffed with full time Accelovance employees. They are capable of handling Phase I-IV outpatient studies. Quality is emphasized through centralized SOPs and corporate training programs. Each clinic is positioned for highly coordinated and/or high volume enrollment, offering the Sponsor predictability and performance assurances.

Patient Management Solutions: more than recruitment and retention . Accelovance proactively recruits patients through its own databases, media and community outreach. Our innovative approaches pre-qualify patients prior to study start to find the right patient for the study. This planning allows for predictable, controlled and timely enrollment along with higher retention and compliance rates. Our proactive Patient Management Solutions are so effective, we will guarantee deliverables.

Clinical Call Center : surveillance, retention, compliance. Accelovance takes ownership of managing the patient through the duration of your program. Let clinically trained agents help manage your patients through their study visit schedule and beyond in a more consistent, quality and controlled way than relying on site staff. Accelovance has managed programs with 400 patients to 19,000 patients in a cost-effective manner by pairing experienced agents who understand clinical research with robust technology that maximize efficiencies and reporting.

Accelovance CHINA: Should a sponsor wish to explore an opportunity in China's rapidly growing pharmaceutical market, Accelovance China has offices in Shanghai and Beijing, PR China providing small pharma/biotech and multinational pharma companies with CRO and market registration services.



Clinical R&D, Clinical Trial Monitoring, Data Management, Inpatient/Outpatient Facilities, Investigational Site/Network, Patient Compliance, Patient Recruitment, Project Management, Protocol Development, Trial Management

Contact Information: 

Accelovance, Inc.
2275 Research Blvd, Suite 700
Rockville, MD, 20850, USA
Phone : 2402384914
Fax : 2402384901
Internet : www.accelovance.com
Email : gsmith@accelovance.com
Contact Person : Garrett Smith