Find vetted vendors, CROs, and technology partners

Connecting More than 1,000 Companies with DIA Members Across 80+ Countries

75

Resources

34

Categories

1188

Listings

63

Recommended

88

Liked

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,...
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...
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,...

ACTIVITY

Featured Content

View All
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.
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
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.
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
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.
Barcode Compliance Guide

Barcode Compliance Guide

Accurate barcodes on healthcare packaging and labeling are just as important as any other information. An incorrect barcode can lead to expensive...

Posted by: Meghann H

Schlafender Hase Schlafender Hase
Don't Miss The Webinar!

Don't Miss The Webinar!

 Multiple time slots: Americas: 6am 10am 2pm EDT Europe: 12pm 4pm 8pm CET   Duration: 30 minutes Sign Up Now  What To Expect: Join us for a...

Posted by: Tina F

Qinecsa Solutions Qinecsa Solutions
Revolutionizing Regulatory Submissions: How AI Templates Simplify IND to NDA

Revolutionizing Regulatory Submissions: How AI Templates Simplify IND to NDA

Regulatory submissions are complex, but drafting them doesn’t have to be. What if you could generate structured, submission-ready content at the...

Posted by: Tammy L , Sr. Marketing Manager

Weave Weave
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
Improving Patient Outcomes and Expanding Healthcare Access

Improving Patient Outcomes and Expanding Healthcare Access

Remote patient monitoring (RPM) is an excellent opportunity to create accessible healthcare that can not only enhance patient outcomes but also...

Posted by: Rebecca M

KORE Connected Health KORE Connected Health
The Role of AI Operations (AI Ops): Charting a Path for the AI Revolution in Associations

The Role of AI Operations (AI Ops): Charting a Path for the AI Revolution in Associations

Given the rapid evolution of AI, dedicating a person to staying abreast of AI developments is crucial to prevent it from becoming a distraction....

Posted by: Andy S

Insight Guide Insight Guide
How Deerfield Optimized Healthcare Advertising Campaigns Using Purplelab®’s Real-World Data Insights

How Deerfield Optimized Healthcare Advertising Campaigns Using Purplelab®’s Real-World Data Insights

Analyzing real-world data (RWD) in pharmaceutical marketing has the power to unearth hidden trends and insights into the overall prescription...

Posted by: Jennie R

PurpleLab PurpleLab
AI solution in case intake

AI solution in case intake

Mark your calendars for September 26th and join us at the Novartis Campus in Basel for the Insife Annual Convention - your calendars for...

Posted by: Natasa B

Insife Insife
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
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
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
Redefining Content Management with Component Content Management Systems (CCMS)

Redefining Content Management with Component Content Management Systems (CCMS)

In today’s rapidly evolving landscape of content management, organizations are increasingly seeking innovative approaches to streamline...

Posted by: Kendal F

Glemser Technologies Glemser Technologies
Upping the Migraine Intelligence Quotient: Real-world data sheds light on prevalence rates, providers and treatment variation

Upping the Migraine Intelligence Quotient: Real-world data sheds light on prevalence rates, providers and treatment variation

Discover groundbreaking insights into migraine prevalence, treatment variations, and healthcare provider dynamics with the PurpleLab Migraine...

Posted by: Jennie R

PurpleLab PurpleLab
(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.

Recommendations

ProPharma
ProPharma
“One of the better medical information providers out...”
Joyce B
Joyce B UK/IE Pharmacovigilance Leader
Veeva Systems
Veeva Systems
“Easy to use, lots of features automated and quick to...”
Amanda R
Amanda R Data Strategist
PharmaCircle
PharmaCircle
“Labels, approval documents and drug formulations....”
So M
So M
See all recommendations →

PREMIUM LISTINGS

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

WHY PARTNER WITH DIA?

GLOBAL REACH

Connect with drug development professionals in 80+ countries

TRUSTED AUDIENCE

Reach credentialed buyers across pharma, biotech, CRO, and regulatory affairs

EVENT INTEGRATION

Get visibility before, during, and after DIA's global conferences