Delivering Excellence in Clinical Trial Solutions
Bringing Your Research to Life

Faster Results

with optimized workflows and real-time insights.

Transparent Pricing

to ensure cost-effective and predictable budgeting.

An Expert Team

for a smoother, stress-free clinical trial experience.

Launch Your Product

to market with speed, precision and confidence.

Regulatory Expertise

With Clinvigilant Research, sponsors gain a dedicated and experienced partner who understands the complexities of clinical trials. Our expertise in clinical trial solutions ensures that your research is conducted efficiently, ethically, and in compliance with regulatory expectations.

Through our clinical trial consulting, we provide strategic insights and guidance, helping you navigate the challenges of clinical development. Our commitment to excellence in clinical trial services empowers sponsors to achieve successful and timely study outcomes.

Who We Work with

Collaborating with innovators to shape the future of healthcare.

The nutraceuticals industry is rapidly growing, with consumers demanding science-backed, high-quality dietary supplements and functional foods. Successfully bringing these products to market requires rigorous clinical validation, strict regulatory compliance, and strategic clinical research to ensure safety and efficacy.

This is where Clinvigilant Research becomes an essential partner, providing expert clinical trial solutions and clinical consulting services to ensure your nutraceutical products meet industry standards and achieve market success.

Nutraceuticals

Dietary Supplements

Vitamins, Minerals, Herbal Extracts

Cognitive & Mental Wellness Supplements

Nootropics, Adaptogens, Omega-3s

Sports Nutrition & Performance Products

Protein Powders, Amino Acids, Recovery Supplements

Beauty & Anti-Aging Solutions

Collagen, Hyaluronic Acid, Antioxidants

Gut Health & Digestive Aids

Probiotics, Prebiotics, Fiber Supplements

Weight Management & Metabolism Boosters

Fat Burners, Appetite Suppressants

Functional Foods & Beverages

Probiotic Yogurts, Fortified Cereals, Energy Drinks

Bringing a medical device to market requires extensive clinical validation, regulatory approval, and post-market surveillance. Clinvigilant Research plays a crucial role in helping medical device companies navigate complex regulations, conduct clinical trials, and accelerate commercialization while ensuring patient safety and compliance through end-to-end (tailored, comprehensive) clinical trial solutions.
Medical Devices

Class I Medical Devices

Low-risk devices requiring general controls (e.g., bandages, surgical instruments, examination gloves).

Class II Medical Devices

Moderate-risk devices requiring special controls (e.g., infusion pumps, blood pressure monitors, diagnostic imaging).

Class III Medical Devices

High-risk devices requiring premarket approval (PMA) (e.g., pacemakers, artificial heart valves, implantable defibrillators).

In Vitro Diagnostic (IVD) Devices

Diagnostic tests and laboratory instruments for disease detection (e.g., PCR test kits, glucose monitors, cancer biomarker tests).

Pharmaceutical companies navigate a complex path in bringing new therapies to market, from early-stage research to post-market surveillance. Clinvigilant Research serves as a trusted partner, offering specialized expertise, cutting-edge infrastructure, and regulatory support at every phase of clinical trials – ensuring efficiency, compliance, and success in drug development.

Pharmaceuticals

Phase I

First-in-Human (Safety & Tolerability Studies)

Phase II

Efficacy & Dose Optimization

Phase III

Large-Scale Safety & Efficacy Trials

Phase IV

Post-Marketing Surveillance

The cosmetic and consumer health industry is evolving at an unprecedented pace, with a rising focus on safety, efficacy, and regulatory compliance. As you venture into launching skincare, haircare, personal care, or wellness products, partnering with a trusted Contract Research Organization (CRO) is key.

With expert clinical trial services and clinical research solutions, Clinvigilant as a reliable CRO can guide your products through rigorous testing, ensuring they meet the highest standards.

Cosmetics

Skincare

Moisturizers, Anti-aging creams, Serums, Acne treatments

Haircare & Scalp Treatments

Shampoos, Conditioners, Hair growth serums

Personal Hygiene & Wellness

Deodorants, Intimate washes, Oral care

Makeup & Beauty Enhancers

Foundation, Lipsticks, Mascaras, BB creams

Sunscreens & UV Protection

SPF lotions, Mineral sunscreens, Tinted sunscreens

Supplements & Nutricosmetics

Collagen, Biotin, Antioxidant blends

What we do

Streamlining Clinical Trials with End-to-End CRO Solutions
End-to-End Clinical Trial Management

End-to-End CRO Clinical Trial Solutions

We offer comprehensive clinical trial and consulting services as a full-service CRO, providing end-to-end solutions that streamline every phase of drug and device development. From study design to regulatory submissions and post-market surveillance, our clinical research consulting ensures efficiency, compliance, and faster market access. We partner with pharmaceutical, biotech, and medical device companies to optimize trials, improve outcomes, and accelerate timelines with tailored clinical trial services. Our range of CRO clinical trial solutions include:

Accelerating Success with Advanced Clinical Trial Solutions

In today’s fast-paced research landscape, achieving efficient and compliant clinical trials is crucial. Our Clinical Trial Solutions are designed to streamline trial management, enhance data integrity, and expedite drug development. With cutting-edge technology and AI-powered eClinical platforms, we ensure seamless data collection, real-time monitoring, and regulatory compliance. By leveraging innovative clinical research solutions, we make clinical trials more efficient, cost-effective, and patient-centric – helping you bring safer, more effective products to market faster.

Tech-Enabled eClinical Platform
Expert Consulting for Clinical Development

Expert Consulting for Clinical Development

We offer clinical research consulting services tailored to pharmaceutical, biotech, and medical device companies, ensuring seamless navigation through the complexities of clinical development, regulatory approvals, and market access. Our industry-leading team specializes in providing clinical consulting services that strategically design, efficiently execute, and ensure full compliance with global regulatory standards.

With expertise in clinical trial consulting services, we help optimize trial designs, enhance operational efficiency, and maintain scientific integrity. Our comprehensive range of consulting services includes:

One Partner, Complete Solutions

How Sponsors Can Rely on Clinvigilant for CRO Excellence

Simplify your clinical trial management with Clinvigilant’s fully integrated, end-to-end CRO clinical trial solutions. From study design and patient recruitment to site operations and data management, we provide everything you need under one roof.

As a Full-Service CRO, our clinical trial services integrate robust eClinical platforms, site capabilities, and patient recruitment expertise to drive efficiency, ensure compliance, and achieve success at every stage of development.

Other Organizations

Traditional CRO does only

Trial Management

eClinical Tech Company does only

eClinical Platform

Recruitment Vendor does only

Central Recruitment

Traditional site does only

Site Network

DCT site provider does only

Virtual Site Solutions

Clinvigilant Research

Trial management

End-to-end project management

eClinical Platform

Our in-house CitrusTM platform includes our EDC, CTMS, and more

Central Recruitment

EHR screening, digital advertising, community engagement, and other innovative approaches

Site Network

Internal and external sites for single- and multi-site trials

Virtual Site Solutions

In-house virtual site staff for hybrid and remote studies

Why we Perfect for Your Successful Clinical Trial

Driving Global Clinical Success with Proven Expertise

Global Reach, Local Expertise

Expanding Borders, Delivering Excellence
Strong foundations in India, US, UK, and Europe ensure worldwide service. Our local knowledge helps navigate regional regulations effectively.

2x Faster Patient Recruitment

Broader Reach for Better Study Outcomes
Access to a broad and diverse patient pool for improved research quality. Our global reach allows us to recruit participants from different demographics.

100+ Successful Regulatory Submissions

Accelerating Approvals with Precision
Expertise in preparing and submitting regulatory documents globally. We optimize submission strategies to expedite approvals and ensure compliance.

120+ Satisfied Sponsors

Trusted by Industry Leaders

Proven track record of delivering excellence in clinical trials. Our commitment to quality and efficiency drives customer satisfaction worldwide.

100% Regulatory Compliance

Navigating Compliance with Confidence

Deep understanding of international regulations for smooth approvals. We streamline compliance processes to avoid delays in clinical trials.

Ready to working with All-In-One CRO?

Together, We Accelerate Breakthroughs – Bringing New Treatments to Patients Faster