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HOW DOES THE DIA MARKETPLACE HELP?

Access pre-vetted expertise without the search overhead. DIA Marketplace delivers quality suppliers curated specifically for life sciences and professional services—reducing sourcing time, minimizing vendor risk, and unlocking member-exclusive discounts. Find the right partner faster, negotiate better terms, and scale your network strategically. One trusted directory. Better outcomes.

ELITE LISTINGS

The Drug Information Association (DIA)—also known as DIA Global—is a nonprofit, member-driven professional association founded in 1964 and headquartered in Washington, D.C. It serves as a global network for life-science professionals across drug,...
Numerof provides customized strategy and implementation solutions for market access, medical affairs, and commercialization challenges across the healthcare industry. With over 30 years’ experience working globally across pharma, device,...
Guiding Your Pharmaceutical Success Through FDA Expertise and SupportThe organization operates as a dedicated division within the U.S. Food and Drug Administration, focusing on providing support and resources to small businesses and the...

ACTIVITY

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Accelerate regulatory submissions with AI, reuse and structured content authoring

Accelerate regulatory submissions with AI, reuse and structured content authoring

Most pharma organizations continue to face persistent challenges in shortening submission timelines. Read this whitepaper to discover how an...

Posted by: Aoife L , Head of Product Marketing

RWS | Tridion One RWS | Tridion One
Informed Consent Form of an IND Submission with AgileWriter™

Informed Consent Form of an IND Submission with AgileWriter™

A small biotech needed an informed consent form (ICF) for an IND submission, with limited lead time following agency feedback. The challenge was...

Posted by: Catlyn S , Business Operations Associate

Synterex, Inc. Synterex, Inc.
Optimizing Expedited Regulatory Pathways to Speed Time to Market

Optimizing Expedited Regulatory Pathways to Speed Time to Market

Speeding therapies to market requires more than faster development; it demands a smarter regulatory strategy. This eBook explores how life...

Posted by: Mathilde H , Demand Marketing Manager

Clarivate Clarivate
Clinical Study Report and Narratives Initial Draft in Record Time with AgileWriter™

Clinical Study Report and Narratives Initial Draft in Record Time with AgileWriter™

A medium-sized biotech faced a tight deadline: a comprehensive Clinical Study Report (CSR) shell and first draft were needed in just two weeks,...

Posted by: Catlyn S , Business Operations Associate

Synterex, Inc. Synterex, Inc.
Poster | The new key player in Digital Transformation and Pharmacovigilance

Poster | The new key player in Digital Transformation and Pharmacovigilance

Digital tools in pharmacovigilance are increasingly valued for their transformative potential. Integrating these tools requires a strategic...

Posted by: Alba L , Marketing Officer

Asphalion S.L. Asphalion S.L.
Compliance-Ready Documents

Compliance-Ready Documents

All too often documents are formatted inconsistently and contain errors. Your team follows standards—but enforcing them costs time, rework, and...

Posted by: Olga M , Business Development Manager

DACHS Computing & Biosciences DACHS Computing & Biosciences
Optimizing Site Selection for Phase III Oncology Clinical Trial

Optimizing Site Selection for Phase III Oncology Clinical Trial

Discover how a pharmaceutical company leveraged advanced analytics to streamline site selection for a Phase III oncology trial, ensuring...

Posted by: Jennie R

PurpleLab PurpleLab
Not Just Any Trial: A Case for Sponsor-Specific Trial Finders

Not Just Any Trial: A Case for Sponsor-Specific Trial Finders

Not all trial finders are created equal. Study aggregate websites may seem patient-friendly, but they often introduce more risk than reward—for...

Posted by: Colleen Y , Head of Marketing

ProofPilot ProofPilot
(White Paper) The Road to Representation in Clinical Research

(White Paper) The Road to Representation in Clinical Research

Innovative development of human drugs, biologics, and medical devices (medical products) and their quick advancement through the United States...

Posted by: Elizabeth P , Business Operations Associate

Synterex, Inc. Synterex, Inc.
(White Paper) This One’s for the Children: Progress in Pediatric Drug Development in the United States

(White Paper) This One’s for the Children: Progress in Pediatric Drug Development in the United States

Prior to the FD&C Act, pharmaceutical companies were not required to provide proof of drug safety or a disclosure of all active ingredients....

Posted by: Elizabeth P , Business Operations Associate

Synterex, Inc. Synterex, Inc.
Unlock Scalability Through High-Performing Technology

Unlock Scalability Through High-Performing Technology

How confident are you that your organization has the right technology in place to support the journey from IND submission to...

Posted by: Abigail G , Chief of Staff

Project Outlier Project Outlier
Investigator Meetings and Site Training: A Necessary Evil, We Can Do Better

Investigator Meetings and Site Training: A Necessary Evil, We Can Do Better

Site training holds a necessary place in clinical research, but the current framework lacks certain elements, hindering the true goals of...

Posted by: Colleen Y , Head of Marketing

ProofPilot ProofPilot
Series topic: Vigilance Medical Device Guidance Part 1- topic: “Vigilance Medical Device Regulations (EU) 2017/745

Series topic: Vigilance Medical Device Guidance Part 1- topic: “Vigilance Medical Device Regulations (EU) 2017/745

Join our insightful webinar exploring the latest developments in the EU medical device vigilance landscape, with industry-renowned specialist...

Posted by: Florence D

Qinecsa Solutions Qinecsa Solutions
Optimize Clinical Trial Enrollment with ProofPilot's Scheduler

Optimize Clinical Trial Enrollment with ProofPilot's Scheduler

Playing phone tag is an unpaid, patient recruitment time-suck, draining up to 40 hours of sites’ precious time each week. Think about what...

Posted by: Colleen Y , Head of Marketing

ProofPilot ProofPilot
Enterprise Mobility Meets Compassion: Curbing Substance Abuse Through Remote Monitoring

Enterprise Mobility Meets Compassion: Curbing Substance Abuse Through Remote Monitoring

The opioid crisis remains a pressing public health concern, with nearly 87,000 drug overdose deaths reported in 2024. Although this reflects a...

Posted by: Rebecca M

KORE Connected Health KORE Connected Health
Enhancing Compliance and Efficiency with Structured Content Authoring

Enhancing Compliance and Efficiency with Structured Content Authoring

In the fast-paced and highly regulated pharmaceutical industry, the efficient management of labeling and regulatory submissions is crucial for...

Posted by: Kendal F

Glemser Technologies Glemser Technologies
The Business Benefits of Using FACTS for the Modeling and Simulation of Clinical Trial Designs

The Business Benefits of Using FACTS for the Modeling and Simulation of Clinical Trial Designs

This white paper will explore the business benefits and case of using the FACTS simulation software for all your clinical trial designs.

Posted by: Shawn A

Berry Consultants Berry Consultants
A Case Study on How to Create and Integrate Multiple Research Libraries to Support Global Teams

A Case Study on How to Create and Integrate Multiple Research Libraries to Support Global Teams

Moderna, a leading mRNA technology company, saw unprecedented growth during the COVID-19 pandemic. Before this, its Medical Affairs teams aligned...

Posted by: Meghann H

ReadCube ReadCube
Recruiting Pediatric Patients for vaccine research

Recruiting Pediatric Patients for vaccine research

Evernorth Health Services, collaborating with a contract research organization (CRO), performed direct-to-patient outreach to recruit patients...

Posted by: Raven D , Marketing & Events Advisor

Evernorth Health Services Evernorth Health Services
FDA Electronic Drug Registration and Listing (eDRLS) using CDER Direct Training Modules

FDA Electronic Drug Registration and Listing (eDRLS) using CDER Direct Training Modules

The eDRLS training modules deliver essential expertise for navigating FDA's electronic Drug Registration and Listing System.The content provides...

Posted by: Meghann H

FDA CDER Small Business and Industry Assistance (SBIA) FDA CDER Small Business and Industry Assistance (SBIA)

Recommendations

ProPharma
ProPharma
“One of the better medical information providers out...”
Joyce B
Joyce B UK/IE Pharmacovigilance Leader
IQVIA
IQVIA
“good engagement in the FSP model for clinical ops”
Laura L
Laura L AVP Region Head Global Clinical Operations EMEA
Imaging Endpoints
Imaging Endpoints
“After bringing Imaging Endpoints into several...”
Angela H
Angela H
See all recommendations →

PREMIUM LISTINGS

Elevate Your Drug Information Accuracy with Premier Regulatory Excellence This company stands at...
Regxia is a unique regulatory and e-publishing consulting firm serving the pharmaceutical and...
Since 1987, Glemser’s team of global technology advisors has been providing software and advisory...
Revolutionizing Pharmacovigilance with Cutting-Edge TechnologyInsife is a leading provider of...
Pioneering Excellence in Drug Information Solutions for a New Era of Healthcare In today's...
Clinical writing and development solution for today's needsSynterex is a global clinical and...
Revolutionizing Clinical Trial Transparency and ComplianceTrialAssure is the global leader in...
Clarivate is a leading global provider of transformative intelligence. We offer enriched data,...
Berry Consultants is a statistical consulting company specializing in innovative clinical trial...
Qinecsa Solutions is a reliable international collaborator uniting top-notch technology and...
In the rapidly evolving landscape of drug development, Weave stands at the forefront with its...
Vivalink's Digital Health Platform for Clinical TrialsVivalink offers a robust digital health...
Empowering Global Pharmaceutical Success Through Innovative Consultancy Solutions This company...
Schlafender Hase delivers an easy-to-use document comparison software for regulated industries to...
Alphanumeric provides a bridge between pharmaceutical companies and HCPs, patients, and...
Simple. Predictable. Clinical Trials.We exist to make clinical trials SIMPLE & PREDICTABLE for...
About CompanyAlphaLife Sciences is an AI-first platform company transforming how novel therapies...
Redefining Health Care for the Modern WorldEvernorth brings the power of innovation and...
Streamline Your Research WorkflowWith ReadCube's literature management system, your...
PurpleLab is a health-tech company driven by one clear philosophy: outcomes matter most. As your...
The Future of Connected Health is NowHealthcare is at a pivotal moment, with IoT adoption...
Pioneering Excellence in Drug Safety and Healthcare SolutionsWe are a trusted partner to the...

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