PRN Pharmaceutical
Research Network, LLC

We Speak Ophthalmology

Welcome to PRN

Thank you visiting. Please allow us to introduce you to our clinical research capabilities and enduring commitment to ophthalmology.

Our Services

PRN’s long-standing partnerships with industry experts provide our clients a well-rounded and comprehensive approach to meet your clinical trial’s needs. 

Project Startup

With over 1000 sites across all 50 US states, PRN ensures the best sites at the time of selection.

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Project Startup

PRN supports you from study conception and planning to protocol development and site selection. With over 1000 sites across all 50 US states, PRN ensures the best sites at the time of selection.

Clinical Monitoring

Our project managers and clinical research associates average at least 10 years' experience in clinical monitoring with deep knowledge of ophthalmology. 

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Clinical Monitoring

Our project managers and clinical research associates average at least 10 years' experience in clinical monitoring with deep knowledge of ophthalmology. They are thorough, detail-oriented, and exhibit superior professional maturity to represent you well.

Site Auditing

Our experienced team supports a range of QA activities to meet your needs.

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Site Auditing

Our experienced team supports a range of QA activities to meet your needs.

Project Completion

PRN study teams are committed to seeing your study through to its completion.    

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Project Completion

PRN study teams are committed to seeing your study through to its completion. This continuity ensures excellence in study involvement and execution.   

Regulatory

PRN understands the complexities of navigating through the requirements of regulatory authorities. 

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Regulatory

PRN understands the complexities of navigating through the requirements of regulatory authorities. We partner with the best regulatory affairs specialists to assist you through this complicated process.

Pharmacovigilance

Our pharmacovigilance experts play a crucial role in clinical trials as they monitor safety and efficacy signals and adverse events, and support safety-related regulatory submissions.

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Pharmacovigilance

Our pharmacovigilance experts play a crucial role in clinical trials as they monitor safety and efficacy signals and adverse events, and support safety-related regulatory submissions.

Medical Monitoring

Hand in hand with our pharmacovigilance experts, our approachable, board certified ophthalmologists provide medical oversight for your trial, with friendly and timely support to investigators and their research personnel, and your entire clinical team.

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Medical Monitoring

Hand in hand with our pharmacovigilance experts, our approachable, board certified ophthalmologists provide medical oversight for your trial, with friendly and timely support to investigators and their research personnel, and your entire clinical team.

Medical Writing

From protocol development to CSR finalization, our medical writers’ detail-oriented, thoughtful and systematic approach provides support where you most need it.

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Medical Writing

From protocol development to CSR finalization, our medical writers’ detail-oriented, thoughtful and systematic approach provides support where you most need it.

Data Management and Biostatistics

PRN partners with the best-in-class ophthalmic specific data management company which also provides biostatistical support and reliable EDC systems to meet your needs.

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Data Management and Biostatistics

PRN partners with the best-in-class ophthalmic specific data management company which also provides biostatistical support and reliable EDC systems to meet your needs.

How PRN Can Help You

Drawing from many years of vigorous participation and a broad network of mature contractors in the ophthalmic community, PRN capably provides all aspects of clinical trial management and consulting.

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