SERVICES

CRO Services

CRO Services: Clinical Trials Management, Regulatory Affairs, Pharmaceutical Drug Development, and More

SRA Global Clinical Development

Mid-size focus...full service reach

Today's pharmaceutical, biotechnology and medical device companies face myriad challenges in trying to bring new drugs, therapies and technologies to those who need them. And timing is crucial in determining which companies are successful in this extremely competitive industry – especially for small-to-mid size biopharmaceutical and device companies. Selecting a development partner with a proven track record and a strong understanding of the entire product development life cycle is essential to improving the overall probability of success and ensuring projects are conducted accurately and efficiently.

SRA Global Clinical Development is a full-service, global CRO with extensive expertise in every phase of the development process and across multiple therapeutic areas. We specialize in working with small to mid-size companies to help them plan for and effectively navigate any or every step of the development process. By combining our comprehensive development services; our in-depth understanding of clinical development, data management and regulatory strategy; and our efficient workflow processes we help give our customers a competitive advantage in the marketplace.

At SRA, we understand that every customer's needs are different and every project is unique. Whether your goal is to develop an information package to increase the value of a candidate for out-licensing or co-development, or to reach corporate milestones for securing next-round financing, we have the resources, the services, and the flexibility to help you achieve your goals. And underlying everything we do is a proven commitment to quality, timeliness, customer service and unparalleled attention to detail. Because, ultimately, reaching the goals of tomorrow begins by focusing on the details today.

SRA offers comprehensive development services in each of the following areas:

  • Clinical Trials
  • Data Sciences
  • Regulatory Affairs
  • Strategic Development Consulting and Planning
  • Drug Safety and Pharmacovigilance
  • Quality Assurance & Audits