Obesity CRO Services

Empowering advancements in obesity treatment through expert trial management and patient-centered care.

Advancing Obesity Treatments with Expert Support

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The obesity drug market is experiencing unprecedented growth, driven by the success of groundbreaking treatments. As more pharmaceutical companies, especially smaller and mid-sized firms, seek to contribute to this dynamic field, the need for expertly managed clinical trials and customized patient support has never been more critical. ProPharma offers specialized services to help you navigate the complexities of obesity clinical trials and compound drug management, ensuring your study and services effective treatments to patients who need them.

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Navigating the Challenges of Rapid Enrollment

Navigating the Challenges of Rapid Enrollment

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Addressing Patient Dropout with Proven Strategies

Addressing Patient Dropout with Proven Strategies

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Designing Trials That Reduce Patient Burden

Designing Trials That Reduce Patient Burden

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Comprehensive Support from Start to Finish

Comprehensive Support from Start to Finish

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Data Visualization

Data Visualization

Navigating the Challenges of Rapid Enrollment

One of the primary challenges in obesity clinical trials or treatment initiation is the speed at which enrollment can occur. Rapid enrollment is a double-edged sword; while it can accelerate your timeline, it also requires a robust monitoring strategy to maintain the integrity of your data and treatment success. ProPharma's experienced team ensures your trial is equipped with a proactive monitoring approach that adapts to fast-paced enrollments, minimizing risks and maintaining the highest quality standards.

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Addressing Patient Dropout with Proven Strategies

In obesity trials, patient dropout can be a significant issue, particularly when participants suspect they are on a placebo. Our team understands the importance of keeping patients engaged throughout the study. We employ evidence-based strategies to minimize dropout rates, including enhanced patient communication, regular check-ins, and innovative patient engagement tools. Our goal is to keep your trial on track, supporting both patients and sponsors by maintaining study continuity and reducing time and cost implications.

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Designing Trials That Reduce Patient Burden

Patient burden is a key factor in both compliance and retention in clinical trials for obesity. ProPharma is committed to designing and executing trials that consider the patient experience at every step. We implement patient-centric trial designs that reduce the burden on participants, whether through simplified protocols, decentralized trials, or flexible scheduling. By focusing on patient needs, we help you achieve higher retention rates and more reliable data, ultimately contributing to better treatment outcomes.

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Comprehensive Support from Start to Finish

ProPharma offers end-to-end support for your obesity clinical trials, from study design to regulatory submissions. Our expertise spans the full spectrum of trial management, including site selection, patient recruitment, data management, and regulatory compliance. With our global reach and deep therapeutic expertise, we are well-positioned to support your trial's success, no matter its size or complexity.

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Data Visualization

Our clients are able to easily digest their fast enrolling data with our unique data visualization tool.

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Accelerate Obesity & Diabetes Clinical Trials and Post Market Treatments

ProPharma has the expertise to accelerate obesity clinical trials by offering comprehensive regulatory support and biostatistical expertise in trial design. In a competitive landscape where many seek obesity drug approvals, our ability to expedite the process is a key differentiator. Additionally, we provide in-house medical and regulatory expertise to efficiently manage and execute these trials, helping you bring your drug to the market faster.

ProPharma also has a proven high-quality worldwide contact center to support obesity treatment management, including customized patient support for clinical trials, commercials, and compounded products. Our medical information and patient support experts deliver excellent patient-centric treatment logistics to ensure that patients meet their goal of weight management safely and effectively.

Decentralized Clinical Trials

ProPharma's decentralized clinical trials (DCTs) offer a more flexible approach to executing trials, allowing sponsors to reach diverse populations and patients who may not have access to traditional trial sites. By utilizing virtual, remote, or hybrid models, ProPharma facilitates easier participation while maintaining regulatory compliance and data integrity. This approach reduces geographic barriers, accelerates patient recruitment, and enhances engagement, leading to more efficient and inclusive trial execution and ultimately improving trial outcomes.

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Why Choose ProPharma?

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Proven Experience

Decades of experience managing obesity clinical trials across diverse populations.

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Patient-Centric Approach

Focused on minimizing patient burden to improve retention and data quality.

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Innovative Strategies

Cutting-edge monitoring and engagement strategies to manage rapid enrollment and minimize dropout rates.

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Global Reach

A worldwide network of sites and regulatory expertise to support your trial across multiple regions.

Ready to Partner with ProPharma?

If you’re committed to advancing innovative obesity treatments and want a partner who understands the unique challenges of obesity clinical trials, ProPharma is here to support your journey. Contact our team today to discover how we can help you bring effective solutions to market.

News & Insights

Pros and Cons of Working with a CRO

July 31, 2025

Pros and Cons of Working with a CRO

Explore the pros and cons of working with a Contract Research Organization (CRO) and how ProPharma sets a new standard in clinical development success.

Understanding PADER: A Key Pharmacovigilance Requirement for the U.S. Market

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Understanding PADER: A Key Pharmacovigilance Requirement for the U.S. Market

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Understanding the Roles of LPPV, QPPV, and the PSMF in Pharmacovigilance: A Guid...

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ProPharma Recognized for AI Excellence at ECCCSA

January 31, 2025

ProPharma Recognized for AI Excellence at ECCCSA

ProPharma wins Silver at ECCCSA for AI innovation in Medical Information, enhancing efficiency and quality in delivering accurate medical information.

ProPharma Appoints Brian Tuttle as Chief Financial Officer

October 21, 2024

ProPharma Appoints Brian Tuttle as Chief Financial Officer

ProPharma appoints Brian Tuttle as CFO to drive financial strategy and accelerate global growth, leveraging his 20 years of life sciences industry experience.

ProPharma Recognized for AI Excellence at ECCCSA

January 31, 2025

ProPharma Recognized for AI Excellence at ECCCSA

ProPharma wins Silver at ECCCSA for AI innovation in Medical Information, enhancing efficiency and quality in delivering accurate medical information.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

September 24, 2024

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

ProPharma honored with Clinical Trials Excellence Award 2024, recognizing their outstanding contributions in the pharmaceutical industry.

Case Study Successfully Executing a Tech Transfer in a Week - ProPharma

July 29, 2025

Successfully Executing a Tech Transfer in a Week

Discover how ProPharma supported a $3B pharmaceutical tech transfer that was executed in just 3 days, relocating five complex product lines. The plan included FDA alignment, pre-approved protocols,...

Case Study Obesity – Accelerated Timelines - ProPharma

July 29, 2025

Obesity – Accelerated Timelines

A mid-size biotech needed fast U.S. market entry for an obesity trial. ProPharma activated 20 sites in 30 days and enrolled 300+ patients—meeting goals despite an increased sample size. Strategic...

Whitepapers Key Compliance Challenges in U.S. Medical Information Services - ProPharma

July 29, 2025

Key Compliance Challenges in U.S. Medical Information Services

For Medical Information (MI) teams navigating today’s evolving regulatory landscape, compliance isn’t just a requirement — it’s a strategic imperative. From managing off-label inquiries to...

Avoiding Common Pitfalls During FDA Inspections

July 29, 2025

Avoiding Common Pitfalls During FDA Inspections

Starting August 2025, the FDA will conduct unannounced inspections at non-U.S. sites. This webinar explores common inspection pitfalls and how to maintain global inspection readiness with expert...

Inside FDA Review: Crafting a Quality ANDA Labeling Submission

July 22, 2025

Inside FDA Review: Crafting a Quality ANDA Labeling Submission

Gain rare, insider insight into the FDA’s expectations for ANDA submissions in this session led by Marshall Florence, PharmD, a former FDA reviewer who recently joined our team. With firsthand...

MAH Essentials: Ensuring Compliance for European Market Entry

July 10, 2025

MAH Essentials: Ensuring Compliance for European Market Entry

This webinar covers the key responsibilities of Marketing Authorization Applicants/Holders and Qualified Persons in the EEA/UK, including pharmacovigilance requirements, legal entity setup, and...

News & Insights

Pros and Cons of Working with a CRO

July 31, 2025

Pros and Cons of Working with a CRO

Explore the pros and cons of working with a Contract Research Organization (CRO) and how ProPharma sets a new standard in clinical development success.

Understanding PADER: A Key Pharmacovigilance Requirement for the U.S. Market

July 28, 2025

Understanding PADER: A Key Pharmacovigilance Requirement for the U.S. Market

Learn about PADER, a crucial pharmacovigilance requirement for U.S. drug safety monitoring, and how it differs from PSUR in ensuring compliance and patient safety. Summarizing the main point of the...

Understanding the Roles of LPPV, QPPV, and the PSMF in Pharmacovigilance: A Guide for Marketing Authorization Holders (MAHs)

July 25, 2025

Understanding the Roles of LPPV, QPPV, and the PSMF in Pharmacovigilance: A Guid...

Learn about the crucial roles of QPPV, LPPV, and PSMF in ensuring effective pharmacovigilance and regulatory compliance for Marketing Authorization Holders (MAHs).

Previous Post Arrow Next Post Arrow
ProPharma Appoints Marshall Florence, Former FDA Labeling Expert, as Vice President, Labeling & Strategy to Advance Strategic Labeling & Promotional Review

July 8, 2025

ProPharma Appoints Marshall Florence, Former FDA Labeling Expert, as Vice Presid...

ProPharma appoints former FDA labeling expert as VP, Labeling & Strategy, enhancing strategic labeling, promotional review, and regulatory consulting expertise to accelerate drug development and...

ProPharma Recognized for AI Excellence at ECCCSA

January 31, 2025

ProPharma Recognized for AI Excellence at ECCCSA

ProPharma wins Silver at ECCCSA for AI innovation in Medical Information, enhancing efficiency and quality in delivering accurate medical information.

ProPharma Appoints Brian Tuttle as Chief Financial Officer

October 21, 2024

ProPharma Appoints Brian Tuttle as Chief Financial Officer

ProPharma appoints Brian Tuttle as CFO to drive financial strategy and accelerate global growth, leveraging his 20 years of life sciences industry experience.

Previous Post Arrow Next Post Arrow
ProPharma Recognized for AI Excellence at ECCCSA

January 31, 2025

ProPharma Recognized for AI Excellence at ECCCSA

ProPharma wins Silver at ECCCSA for AI innovation in Medical Information, enhancing efficiency and quality in delivering accurate medical information.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

September 24, 2024

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

ProPharma honored with Clinical Trials Excellence Award 2024, recognizing their outstanding contributions in the pharmaceutical industry.

Previous Award Arrow Next Award Arrow
Case Study Successfully Executing a Tech Transfer in a Week - ProPharma

July 29, 2025

Successfully Executing a Tech Transfer in a Week

Discover how ProPharma supported a $3B pharmaceutical tech transfer that was executed in just 3 days, relocating five complex product lines. The plan included FDA alignment, pre-approved protocols,...

Case Study Obesity – Accelerated Timelines - ProPharma

July 29, 2025

Obesity – Accelerated Timelines

A mid-size biotech needed fast U.S. market entry for an obesity trial. ProPharma activated 20 sites in 30 days and enrolled 300+ patients—meeting goals despite an increased sample size. Strategic...

Whitepapers Key Compliance Challenges in U.S. Medical Information Services - ProPharma

July 29, 2025

Key Compliance Challenges in U.S. Medical Information Services

For Medical Information (MI) teams navigating today’s evolving regulatory landscape, compliance isn’t just a requirement — it’s a strategic imperative. From managing off-label inquiries to...

Previous Resource Arrow Next Resource Arrow
Avoiding Common Pitfalls During FDA Inspections

July 29, 2025

Avoiding Common Pitfalls During FDA Inspections

Starting August 2025, the FDA will conduct unannounced inspections at non-U.S. sites. This webinar explores common inspection pitfalls and how to maintain global inspection readiness with expert...

Inside FDA Review: Crafting a Quality ANDA Labeling Submission

July 22, 2025

Inside FDA Review: Crafting a Quality ANDA Labeling Submission

Gain rare, insider insight into the FDA’s expectations for ANDA submissions in this session led by Marshall Florence, PharmD, a former FDA reviewer who recently joined our team. With firsthand...

MAH Essentials: Ensuring Compliance for European Market Entry

July 10, 2025

MAH Essentials: Ensuring Compliance for European Market Entry

This webinar covers the key responsibilities of Marketing Authorization Applicants/Holders and Qualified Persons in the EEA/UK, including pharmacovigilance requirements, legal entity setup, and...

Previous Webinar Arrow Next Webinar Arrow