With the critical nature of your data, why would you choose anyone other than Mindlance Clinical to manage your studies? Our Data Management team includes many of the top minds in the industry. Over the last decade it became evident you need more than basic knowledge of clinical trials databases to ensure data integrity and the successful management of your study data. With a broad range of knowledge requirements from monitoring and reviewing patient records, handling queries for data problems, to tracking validation discrepancies, resolving data errors or performing validity checks based on protocol specifics, Mindlance Clinical provides the specialized consultants and permanent placements needed to maintain the integrity of your study.

Mindlance Clinical's Data Management Team consists of resources to fulfill the following requirements:

• Clinical Data Managers
• Clinical Data Analysts
• Clinical Data Support Specialists
• SAS Programmers
• Biostatisticians
• Bioinformatists

With the additional emphasis placed on time-to-market and reduction in the drug development life cycle, clinical support becomes even more crucial to the success of your study and ultimately the ability to commercialize your product. Due to the ever changing complexities associated with supporting a successful study from the inception of drug development planning to regulatory submissions; needs for specialized medical writing are increasing. This includes study reports, protocols, regulatory submissions and multi-faceted quality assurance programs. Mindlance Clinical's Clinical Support Practice concentrates on fulfilling your needs in supporting clinical trials. Mindlance Clinical recruits the brightest talent in the industry including:

• Medical Writers
• Regulatory Affairs Auditors
• Quality Assurance Analysts
• Validation Specialists