About CurAccel

Scale a new peak of clinical trial excellence with CurAccel Clinical Trial Contract Research Organization (CRO)
CurAccel supports small and mid-sized biotechnology, pharmaceutical and medical device companies on their journey through the entire clinical trial process. We are known for providing the facts that are required for companies to make important decisions. Our renowned quality control process runs through everything that we do and deliver.

Our contract research organization journey began in 2012 and our team is comprised of medical physicians and clinical research professionals with years of research experience both in US and global clinical trial execution. During this time, we have expanded to ensure that we can offer clients access to:

• A diverse patient population
• Economized study execution
• High quality clinical research services
• Global regulatory support

We can research most areas, but our forte is:

• Oncology
• CNS
• Cardiology
• Infectious Diseases
• Pulmonology
• Rare Diseases

We offer all services required to pass a new prospective drug, medical device or nutraceutical through the various phases of clinical trial. Our services include:

• Project Management
• Clinical Monitoring
• Data Management
• Biostatistics
• Medical Writing
• Medical Management
• Contract Management
• Quality Management
• Regulatory Affairs
• Grant Management

CurAccel is a minority, women-owned business and we pride ourselves on delivering highly regarded accurate reports and an exceptional level of customer service.

Contact us today to discuss your contract research organization needs.

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Website
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Employees
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Industry
Pharmaceuticals
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Headquarter
6 Penns Trail, Suite 201, Newtown, PA 18940, US
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Founded
2012
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Keywords
Quality Assurance, Project Management, Medical Devices, Remote Monitoring, Clinical Monitoring, Phase I-Iv, Regulatory Affairs, Protocol Development, Clinical Trial Management, Global Clinical Development, Safety And Pharmacovigilance, Early Clinical Development, Biometrics And Data Sciences, Regulatory Affairs And Medical Writing, Cro Oversigh, Diagnostic Device Trials, Ind Filing Support, Protocol Rescue, Cannabinoid Clinical Trials, Nutraceutical Labeling

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