Our Story

Founded with the vision of enhancing the clinical trial process, we have evolved into a trusted partner for pharmaceutical companies, Sponsors, CROs, and research institutions. Over the years, we've built a strong foundation of expertise in clinical trial management, ensuring that trials are executed efficiently, ethically, and with the highest standards of quality.

Founded on 20 Feb 2020 by Dr. Ujwala Kulkarni and Dr. Renuka Madnurkar, our Clinical Trial Organization is dedicated to collaborating with Sponsors, CROs and Hospitals to drive advancements in the drug development industry.

Purpose in the Clinical Trial Ecosystem

As a Site Management Organization (SMO), our purpose is to bridge the gap between sponsors and research sites. We manage the operational aspects of clinical trials to ensure they are conducted smoothly, on time, and in compliance with all regulatory requirements.

By offering comprehensive services such as site selection, patient recruitment, and data management, we empower both sponsors and research teams to focus on what matters most—delivering reliable results that improve patient care and advance medical research.

Mission, Vision & Core Values

Guiding principles that drive our commitment to excellence

Our Mission

Be #1 SMO in the Clinical Trial Industry of Maharashtra and the Global Leader in Clinical Trial Solutions in collaboration with Global & Domestic Leaders of drug industry to shape the future of Clinical Research by driving innovation and Empowering Clinical Trials with Speed and Precision

Our Vision

Safety of subject is priority & Quality of data is the standard

Integrity

Upholding the highest ethical standards in every aspect of clinical trial management, ensuring transparency, honesty, and accountability in all our actions.

Excellence

Delivering superior service and outcomes by continuously improving our practices and adhering to rigorous quality standards.

Collaboration

Fostering strong, supportive relationships with sponsors, research sites, and clinical teams, recognizing that teamwork is essential for success.

Patient-Centricity

Prioritizing patient safety, comfort, and well-being throughout every trial phase, ensuring that their health remains the top concern.

Innovation

Embracing new technologies, methodologies, and practices to streamline the trial process, improve data accuracy, and speed up the time to results.

Compliance

Strictly adhering to regulatory requirements and Good Clinical Practice (GCP) guidelines, ensuring that every trial is executed within the boundaries of industry standards.

Efficiency

Maximizing the impact of each clinical trial by optimizing processes, reducing unnecessary delays, and improving overall study timelines.

Our Leadership Team

Experienced professionals dedicated to advancing clinical research

Dr. Ujwala Kulkarni

Dr. Ujwala Kulkarni

BAMS with PGDCR and MA in Clinical Psychology
Owner and Founder

Dr. Ujwala Kulkarni has over 30 years of medical experience and clinical research leadership.

Dr. Renuka Madnurkar

Dr. Renuka Madnurkar

BHMS with PGDCR
Owner and Founder

Dr. Renuka Madnurkar has over 13 years of experience in clinical research and site management.

Why Choose AH&R?

Each of our leaders is dedicated to fostering a culture of excellence, collaboration, and innovation

Proven Track Record

Successfully completed 70 trials in different therapeutic areas with potential Principal Investigators and Global and Domestic sponsors.

Comprehensive Experience

Extensive experience in Phase I to Phase IV, BA/BE trials and PMS Trials, and have participated in US FDA audits, QA audits, and Sponsor audits.

Technology Expertise

Skills to handle different software's for Electronic Data Capture and experience in sample handling for different central laboratories.

Expanding Across Maharashtra

We propose to support Hospitals in the development and operationalization of a full-fledged Clinical Research Department. We assist hospitals to develop a trial site, Site initiation of activities, Source documentation, CRF & eCRF entry, Maintaining of Trial Master File, Record of Investigational Products, Site to EC communication, SAE notification process and assist to PI and site to maintaining the compliances of study protocol & regulatory guidelines.

SMO appointed trained CRCs at respective sites for smoothening the project work & proper documentation. We believe that this collaboration will be mutually beneficial, enhancing Hospital's research capabilities and expanding its footprint in clinical research. Now team has decided to expand the network all over Maharashtra State.

Ready to Work with Our Expert Team?

Contact us to learn how our experienced leadership can support your clinical trial needs.