Overview of BCRS - Why BCRS?

At BCRS we are dedicated to making certain your studies proceed smoothly, on schedule, and in compliance with regulatory standards. We take pride in our “hands on” approach and enjoy not just working with our clients but partnering with them.

Working with our team, you will have access to more than 50 years of successful industry experience focused on both Phase I clinical and bioanalytical studies, including extensive CRO experience. With site qualification and selection, in-life monitoring for GCP/GLP compliance, and final study data review, we have the expertise to ensure the quality and integrity of your study results.

Assuring your data is compliant with current Food and Drug Administration requirements prior to submission may avoid lengthy and costly delays in the review process. We understand the power of coordinated pre-study planning, efficient execution, and post-study auditing, to maximize the probability of a successful outcome.

Under our direction, you can be confident your study is conducted in strict compliance with the protocol, Standard Operating Procedures, and current regulatory requirements.

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