R&D CONSULTING

Prime your drug development program for rapid innovation

Drive key decisions from indication selection and asset optimization through study design and planning. Leverage IQVIA’s industry acumen, unparalleled data, comprehensive AI-enabled solutions and transformative technology  to support your drug development program across the research and development continuum.

YOUR PARTNER FOR INNOVATION

Optimize drug discovery and development

Navigate the complicated terrain of drug development, mitigating regulatory risks along the way, with IQVIA’s unparallelled data and transformative technology. Realize your program’s potential with tailored strategies to reduce risks and enhance your clinical development.

Confidently face the most complex R&D challenges with applied data, technology, AI/ML and expertise

OPTIMIZING YOUR PORTFOLIO

Optimize portfolio strategy and manage risks for success

By strategically managing your R&D portfolio, you can ensure your projects align with your organization's goals and market demands. Enhance your portfolio strategy and manage risk effectively with evidence-based decisions. Understand market dynamics, evaluate pipeline assets and prioritize products based on their potential impact to achieve success across your portfolio.

ADVANCING INNOVATION

Accelerating drug development

Gain a competitive edge in your drug development program with structured, yet flexible, solutions from indication selection to pivotal study designs. Experience the impact of AI-powered integrated asset development — synchronizing your regulatory, clinical and commercial strategies.

EXPERT REGULATORY STRATEGY CONSULTING

Strategic market entry and risk management solutions

Ensure compliance, reduce risks and boost productivity for your market entry. Our experts anticipate regulatory changes, craft proactive strategies and prepare you for interactions with regulatory bodies. We support you through product development and enhance your global regulatory engagements.

OPTIMIZED STUDY DESIGN DEVELOPMENT

The power of optimized design in clinical trials

A well-designed protocol minimizes patient burden, enhances recruitment and retention and improves overall trial performance. Make evidence-based decisions throughout the design development pathway to reduce complexity and minimize risk. Leverage IQVIA’s  study design solutions to optimize your clinical trials, patient engagement strategies, endpoint selection, statistical analysis planning and regulatory support.

OPTIMIZE YOUR TRIAL FOR RECRUITMENT

Leverage global data insights for optimized strategies

By pinpointing the most suitable mix of countries and sites at the outset of your planning phase, we can help you to craft a more informed enrollment strategy and assess the viability of your study before it goes live. Incorporate comprehensive considerations for representativeness and recruitment tactics utilizing our insights to access global patient populations, gauge physician expertise and evaluate site-level competition.

LET’S TALK
Optimize drug development with IQVIA’s applied data, AI/ML solutions and domain expertise
Enhance your drug development with IQVIA’s expert consulting, combining industry knowledge, AI and data-driven strategies to manage regulatory challenges, optimize clinical programs and achieve success. Partner with us for informed decisions and accelerated development.

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Learn more about other IQVIA consulting  solutions that can support your R&D program.

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