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Welcome To Navatio Pharma
Excellence in End-to-End Pharmacovigilance Solutions – Your Reliable Pharmacovigilance Specialist
About Company
About Navatio Pharma
Navatio Pharma Solutions is a leading global contract research organization (CRO) specializing in pharmacovigilance, materiovigilance, medical writing, regulatory affairs, and QPPVs. We are dedicated to advancing drug and medical device safety by delivering cutting-edge, compliant, and high-quality solutions tailored to the needs of pharmaceutical, biotech, and healthcare organizations around the globe.
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What we provide
Our Services
Pharmacovigilance Services
Comprehensive drug safety solutions ensuring regulatory compliance and patient well-being...
Pharmacovigilance System Set-Up & Maintenance
End-to-end support in establishing and maintaining robust PV systems tailored to regulatory requirements...
Medical Information Services
24/7 expert-driven support for medical inquiries and adverse event reporting ...
Veterinary Pharmacovigilance
Ensuring the safety of veterinary medicines through risk management and adverse event monitoring...
Cosmetovigilance
Monitoring and managing adverse effects of cosmetic products to ensure consumer safety. ...
Medical Writing Services
Regulatory-compliant medical and scientific writing, including safety reports and clinical documents...
Regulatory Operations & Publishing
Expert guidance on global regulatory compliance, dossier submissions, and approvals. ...
Materiovigilance for Medical Devices
Safety monitoring of medical devices to detect, assess, and prevent adverse events. ...
Innovation
Navatio Pharma in Innovation and Excellence
At Navatio Pharma, we offer specialized support services tailored to the unique needs of both early-stage and established pharmaceutical, biopharmaceutical, medical device, and cosmetic manufacturing companies. Our expertise in critical functions empowers you to navigate the complexities of the research and development lifecycle, ensuring you meet and surpass industry demands.
We understand that success in the pharmaceutical and biopharmaceutical industries requires precision, compliance, and efficiency. That’s why we provide comprehensive support, from preclinical research and regulatory strategy to quality assurance and post-market surveillance. Our team works closely with clients to develop tailored solutions that enhance research effectiveness, mitigate risks, and optimize costs, all while ensuring regulatory compliance.
330
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Clients in 2024
156
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Highly Qualified Experts
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Ratings out of 5
Why Choose Us?
Expertise
It sounds like you're highlighting your team's expertise in global regulatory compliance. Do you want to expand on specific industries, regions, or regulatory frameworks you specialize in? I can help refine the messaging to make it more compelling.
Customized Solutions
You're emphasizing customization and alignment with client needs, which is great. Would you like to add a specific example or mention key regulatory frameworks (e.g., CDSCO, FDA, EMA, MHRA) to strengthen the message?
Proven Track Record
We have successfully guided numerous clients across the pharmaceutical, medical device, and biotechnology sectors through the regulatory approval process, ensuring compliance with FDA, EMA, and other global authorities for timely market entry.
Key Features of Navatio Pharma
01
Comprehensive Service Portfolio
This diverse service offering enables them to support pharmaceutical, biopharmaceutical, medical device, and cosmetic manufacturing companies effectively.
02
Experienced Team
With over 35 years of experience, Navatio Pharma 's team of highly qualified experts is dedicated to helping companies navigate the complex demands of the R&D lifecycle.
03
Global Reach
Navatio Pharma serves clients worldwide, assisting small, medium, and large pharmaceutical and biotech organizations in satisfying international regulatory requirements.
04
Commitment to Excellence
The company prides itself on its core values of transparency, adaptability, and trust, working closely with clients to deliver tailored solutions that meet and exceed industry demands.
What Makes Us Successful
01
Understanding Client Requirements
We begin by closely collaborating with our clients to gain an in-depth understanding of their specific needs, objectives, and regulatory challenges.
02
Strategic Planning & Consultation
Our experts develop customized strategies and roadmaps to align with industry best practices and regulatory frameworks.
03
Execution & Implementation
We execute projects with precision, leveraging our expertise in Regulatory Affairs, Medical Writing, Pharmacovigilance, and more.
04
Compliance & Quality Assurance
We ensure that all deliverables meet the highest standards of quality, regulatory compliance, and safety.
Our Blog
Our Latest News & Blog
14
March
Literature Monitoring
In the ever-evolving pharmaceutical industry, ensuring drug safety and regulatory compliance is of utmost importance. Literature Monitoring serves.
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09
Jan
Key Pharmacovigilance
Pharmaceutical companies navigate an increasingly intricate regulatory landscape where drug safety and compliance remain paramount.
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19
March
Pharmacovigilance for Orphan Drugs
Rare diseases, also known as orphan diseases, affect fewer than 1 in 2,000 individuals in Europe, impacting approximately 27 to 36 million.
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