About Sas research llc
SAS Research LLC: A Leading Provider of Phase 1 Clinical Trials Research Services
SAS Research LLC is a renowned clinical research organization that specializes in providing top-notch facilities and services for Phase 1 clinical trials research studies. The company has been in operation for several years, and its team of experts has extensive experience in conducting clinical trials across various therapeutic areas.
At SAS Research, we understand the importance of conducting safe and efficient clinical trials to bring new drugs and treatments to market. Our state-of-the-art facilities are designed to meet the unique requirements of Phase 1 studies, including early-stage drug development, safety assessments, pharmacokinetics (PK), pharmacodynamics (PD), bioequivalence (BE), food-effect studies, drug-drug interaction (DDI) evaluations, first-in-human (FIH) studies, and more.
Our Facilities
We have two modern facilities located in San Antonio and Austin that are equipped with advanced technologies to support our clients' needs. Our San Antonio facility is a 30-bed unit with private rooms for each participant. It features a fully equipped pharmacy with temperature-controlled storage areas for investigational products. We also have an on-site laboratory that provides real-time results for PK/PD analyses.
Our Austin facility is a 24-bed unit with similar amenities as our San Antonio location but offers additional capabilities such as telemetry monitoring systems that allow us to monitor participants' vital signs remotely.
Both our facilities are staffed by highly trained professionals who ensure the safety and well-being of study participants while maintaining strict adherence to regulatory guidelines.
Our Services
At SAS Research LLC, we offer comprehensive services tailored to meet the specific needs of each client's study design. Our services include:
- Protocol Development: We work closely with sponsors to develop protocols that meet regulatory requirements while ensuring scientific validity.
- Regulatory Support: We provide guidance on regulatory submissions such as Investigational New Drug Applications (INDs) or Investigational Device Exemptions (IDEs).
- Clinical Operations: Our team of experts manages all aspects of clinical operations, including participant recruitment, screening, and enrollment.
- Data Management: We use advanced technologies to collect and manage data in real-time, ensuring accuracy and completeness.
- Biostatistics: Our biostatisticians provide statistical analysis plans and support for data interpretation.
Our Team
At SAS Research LLC, we have a team of highly qualified professionals with extensive experience in conducting Phase 1 clinical trials. Our team includes:
- Medical Directors: Our medical directors are board-certified physicians who oversee the safety and well-being of study participants.
- Clinical Research Coordinators (CRCs): Our CRCs are responsible for managing all aspects of the study from participant recruitment to data collection.
- Regulatory Affairs Specialists: Our regulatory affairs specialists provide guidance on regulatory submissions to ensure compliance with FDA guidelines.
- Biostatisticians: Our biostatisticians provide statistical analysis plans and support for data interpretation.
Why Choose SAS Research LLC?
Choosing SAS Research LLC as your partner for Phase 1 clinical trials research studies comes with several benefits. These include:
- State-of-the-art facilities equipped with advanced technologies
- Highly trained professionals with extensive experience in conducting clinical trials
- Comprehensive services tailored to meet each client's specific needs
- Strict adherence to regulatory guidelines
- Real-time data collection and management using advanced technologies
Conclusion
SAS Research LLC is a leading provider of facilities and services for Phase 1 clinical trials research studies. With state-of-the-art facilities located in San Antonio and Austin staffed by highly trained professionals, we offer comprehensive services tailored to meet each client's specific needs while maintaining strict adherence to regulatory guidelines. Contact us today to learn more about how we can help you bring new drugs or treatments safely and efficiently through early-stage development.
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