For Sponsors & CROs

Streamlining clinical trials with speed, precision, and regulatory excellence

Why Choose AH&R as Your SMO Partner?

At AH&R, we specialize in streamlining the clinical trial process, ensuring trials are conducted efficiently, on time, and in full regulatory compliance.

Our dedicated approach minimizes delays by leveraging experienced staff, advanced technologies, and proven processes. From rapid site activation to optimized patient recruitment and retention strategies, we ensure smooth trial operations, delivering high-quality results while reducing risk and maximizing time-to-market for new treatments.

Our Commitment

We prioritize clear communication, transparency, and collaboration. Our goal is to work closely with you, providing the support you need to meet and exceed your research objectives.

Key Benefits of Partnering with AH&R

Proven advantages that accelerate your clinical trials and ensure success

Rapid Site Activation

We accelerate the site setup process by ensuring all logistical, regulatory, and staffing requirements are met quickly and efficiently. Our streamlined processes reduce time to initiation, helping you start trials faster.

Experienced Staff

Our highly trained, experienced team brings deep expertise in clinical trials, site management, patient recruitment, and regulatory compliance, ensuring your study is in expert hands from start to finish.

Strong Patient Pools

We have access to diverse, pre-screened patient pools, ensuring that recruitment timelines are minimized. Our patient engagement strategies help keep participants enrolled throughout the study, reducing dropout rates.

Compliance Excellence

We maintain strict adherence to GCP, FDA, and other regulatory standards, ensuring that all trials are executed with the highest level of quality and compliance, reducing the risk of delays and ensuring data integrity.

Comprehensive Service Portfolio for Sponsors & CROs

End-to-end clinical trial management solutions tailored to your needs

Core SMO Services

Site Selection & Feasibility

Strategic site selection based on therapeutic area expertise, patient demographics, and historical performance data to ensure optimal study execution.

Site Initiation & Management

Complete site setup including regulatory submissions, staff training, equipment installation, and ongoing operational management throughout the study.

Performance Monitoring

Real-time monitoring of site performance metrics including enrollment rates, protocol compliance, data quality, and timeline adherence.

Specialized Support

Data Management & EDC

Expertise with multiple EDC systems, real-time data monitoring, query resolution, and database lock activities ensuring high-quality data delivery.

Regulatory Affairs

Complete regulatory support including IEC submissions, CDSCO approvals, SAE reporting, and regulatory correspondence management.

Laboratory Coordination

Central and local laboratory coordination, sample logistics, chain of custody management, and result tracking for all study assessments.

Proven Track Record

70+
Completed Studies
20+
Pharmaceutical Partners
12+
CRO Partners
100%
Regulatory Compliance

What Our Partners Say

Testimonials from satisfied sponsors and CROs

"Partnering with AH&R was a game-changer for our clinical trials. Their site management expertise and quick responsiveness to challenges ensured that we stayed on schedule, and their team was always available to address any issues. The level of professionalism and attention to detail has been outstanding."

Director of Clinical Research Organization

"The team at AH&R became an invaluable extension of our own. They provided the staffing, regulatory support, and quality assurance we needed to successfully manage our Phase III trials. Their hands-on approach and deep knowledge of clinical trial logistics helped us achieve our goals ahead of schedule."

VP of Operations

"We've worked with several SMOs in the past, but the expertise and level of service provided by AH&R is unmatched. Their focus on compliance and their proactive communication kept our trials running smoothly, ensuring that we met every milestone without compromising on quality."

Clinical Project Manager, CRO

"Excellence source data and proper electronic data entry within time period."

CRO

"First SMO to conduct Phase I trial in Marathwada region with excellent sample collection and data integrity."

CRA

"Trial completion with protocol compliance and minor Protocol deviation."

CRO

Partnership Process

Simple steps to start your collaboration with AH&R

Initial Consultation

Discuss your study requirements, timeline, therapeutic area, and specific needs to develop a customized partnership proposal.

Proposal & Agreement

Receive detailed proposal including site capabilities, timelines, budget, and service level agreements tailored to your study.

Site Activation

Rapid site setup with regulatory submissions, staff training, and all necessary preparations for study initiation.

Study Execution

Comprehensive study management with regular reporting, monitoring, and proactive communication throughout the trial.

Trusted by Leading Organizations

Our partners include top pharmaceutical companies and CROs globally

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Ready to Partner with AH&R?

Join leading pharmaceutical companies and CROs who trust AH&R for their clinical trial management needs. Let's discuss how we can accelerate your trials and ensure success.

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