Our Team: The Driving Force Behind Ardent

At Ardent Clinical Research Services, our greatest strength lies in our people—a team of highly qualified, experienced, and dedicated professionals who bring deep domain expertise and unwavering commitment to every project we undertake. With specialists in clinical operations, data management, quality assurance, and project management, our team is well-equipped to handle the demands of global clinical research with precision, efficiency, and integrity.

Meet Our Core Team
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Meet Our Team

At Ardent Clinical Research Services, our strength lies in our highly qualified and experienced team of professionals who bring together a wealth of knowledge across all facets of clinical research.

Our team is composed of clinical research experts, medical professionals, regulatory specialists, data managers, and project leaders, each dedicated to upholding the highest standards of quality, ethics, and compliance. With strong academic backgrounds and real-time industry experience, they are equipped to handle the complexities of clinical trials with precision and efficiency.

What sets our team apart is their collaborative approach, attention to detail, and unwavering commitment to scientific excellence and client satisfaction. From study design to execution, monitoring to data analysis, our team ensures that every project is conducted with accuracy, transparency, and integrity.

Together, we drive innovation, ensure regulatory compliance, and deliver successful outcomes for our clients — making Ardent a trusted partner in clinical research.

A visionary leader with over a two decades of clinical research experience, driving the company's strategic and operational excellence.

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Mr. Chandu Devanpally
Founder & CEO, Operations Head — MSc Biochemistry | PGDCR

Expert in managing clinical trial data systems and coordinating multi-functional trial activities with efficiency.

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Ms. Swati Kurandale
Head, Data Management and Operations — M. Pharmacy | PGDCR

Oversees quality assurance processes, ensuring compliance and regulatory alignment across all trials.

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Ms. Pratiksha Magdum
QA Associate & Auditor — MSc Medical Information Management

Skilled for end-to-end oversight of clinical trials, ensuring studies are delivered on time, within scope, and in compliance with regulatory standards.

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Mrs. Rahel Shelke
Project Manager — MSc Microbiology | PDGCR

Plays a key role in Project Management planning, executing, and monitoring clinical trials. Skilled in managing trial timelines, resources, and sponsor communications across therapeutic areas.

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Ms. Simran Belekar
Project Manager — MSc Microbiology | PDGCR

Responsible for designing statistical analysis plans and ensuring robust methodology in clinical trials. Skilled in data interpretation, statistical modelling, and validating study results to support regulatory submissions.

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Ms. Priti Navi
Bio-statistician — MSc Bio Statistics

Ms. Pallavi, our in-house Interactive Web Response System (IWRS) expert, who brings extensive experience in managing complex clinical trial operations with precision and efficiency.

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Ms. Pallavi
Developer — MCA

Ms. Pooja Patil plays a critical role in developing and validating eCRFs that ensure accuracy, compliance, and seamless data flow throughout the clinical trial lifecycle.

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Ms. Pooja Patil
Lead Developer — MCA

Ms. Tanuja, our dedicated Sr. Data Manager and Analyst, who plays a vital role in ensuring the accuracy, integrity, and usability of clinical trial data at Ardent Clinical Research Services.

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Ms. Tanuja
Sr. Data Manager and Analyst — M Pharmacy

This multi-disciplinary team forms the backbone of Ardent’s success—ensuring that each study is conducted with the highest standards of quality, ethics, and scientific integrity. With decades of collective experience, our team continues to drive innovation, client satisfaction, and regulatory excellence across all clinical research initiatives.

WORKING PRINCIPLES

Our Working Principles

At Ardent Clinical Research Services, our work is grounded in a set of core principles built around ethics, quality, and the well-being of patients and clinical trial subjects.

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Our Foundation

These foundational values guide every aspect of our operations and have helped us earn a reputation for reliability, client-centricity, and flexibility in the clinical research industry.

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We are recognized for our fully integrated service offerings, extensive research experience, and a highly committed team that drives excellence across every project.

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For Our Customers

To meet the present and future needs of our clients through a combination of expert talent, state-of-the-art infrastructure, and cutting-edge technology.

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To build flexible and collaborative partnerships that emphasize quality, affordable innovation, and high productivity.

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For Our Stakeholders

To uphold the highest ethical standards, prioritizing patient safety, physician collaboration, and provider professionalism.

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To offer our employees a safe, inclusive, and growth-oriented work environment that encourages the development of scientific, managerial, and leadership competencies.

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Our Commitment

These guiding principles form the backbone of our operations and ensure that we continue to deliver value to our clients, stakeholders, and the broader healthcare ecosystem with integrity and impact.

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Metabolic & Endocrine Disorders

Semaglutide Injection – Type 2 Diabetes Mellitus (T2DM)
Dapagliflozin + Vildagliptin + Metformin – Phase IV (T2DM)
Fixed Dose Combination of DAPA + Gliclazide – T2DM (Product approved – Nov 2023)
Vildagliptin + Pioglitazone Hydrochloride Tablets (50/15 mg) – Approved by DCGI (2022)
Remogliflozin vs. Dapagliflozin – Glycemic Variability (REMIT-GV Study)
Teneligliptin – TIR Metric using CGM (TOP-TIR Study)
Type 2 Diabetes – 2 Trials with Gymne Mag-D
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Injectables & Drug Delivery Systems

  • Chemotherapy Induced Nausea Vomiting (CINV) – Phase III Study
  • Needle-Free Injection System Trials:
  • HPV (Cervavac Vaccine)
  • MMR (Tresivac Vaccine)
  • Hexavalent Vaccines
  • All PMS Vaccines for infants aged below 6 months & 6–24 months
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Oncology

NUVASTATIC – 4 Studies for Breast & Colon Cancer

Capecitabine 500 mg – For EMEA and MHRA submission

Chemotherapy-Induced Fatigue:

In TNBC patients using NUVASTATIC (Phytopharmaceuticals)

In Colorectal Cancer patients using NUVASTATIC

FCM (Ferric Carboxymaltose) – 196 patients (EMEA submission)

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Urology & Men's Health

Silodosin + Solifenacin – Phase III (BPH)

Benign Prostate Hyperplasia – With Pro-Plus (Publication under review)

Oligospermia – 2 Trials using CoQ-10

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Cardiology & Hypertension

  • Telmisartan 40 mg vs. Cilnidipine 10 mg – ABPM Study for 24-hour effect
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Liver Disorders & Hepatology

Nor-UDCA – For NASH (Under regulatory approval)
No-UDCA – For NAFLD (Completed)
Polyherbal Formulations – For NAFLD (Completed and under publication)
Non-Alcoholic Fatty Liver Disease – (Completed)
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Phytopharmaceuticals & Herbal Studies

  • Ashwagandha (DSTR) – Moderate Stress Management
  • Yeshtimadhu (AYUSH – COVID-19) – Completed
  • Gudichipipali (AYUSH – COVID-19) – Completed
  • COVID-19 Antiviral (Patented Herbal Product) – Completed & submitted to AYUSH
  • OBINIL – Obesity Management
  • Ashwagandha, Amaranthus – BE Studies – Completed
  • Canker Sore Gingivitis – Completed
  • Herbal Cough Syrup (Russian Product) – Completed
  • Metabolic Syndrome Study – Completed
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COVID-19 Clinical Trials

MOLNUPIRAVIR – Study with 1218 patients (Sponsor: MSN Laboratories)
Proof of Concept Study – Long-term antibody sustainability (Under publication)
CSIR-IIIM/AYUSH Ministry Trials – 2 COVID-19 Phase II Trials awarded
COVID-19 Antiviral Phase I & Phase I Clinical Trials – In Mild to Moderate Patients
COVID-19 (Ketone Bodies) – Completed (Under Publication)
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Other Therapeutic Areas

Gut Health in CKD with Diabetes – (Under publication)

Needle-Free Vaccination Trials – For multiple age groups and vaccine types

OMEGA-3 BE Study – Completed