Find vetted vendors, CROs, and technology partners

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

75

Resources

34

Categories

1189

Listings

65

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

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,...
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...

ACTIVITY

Featured Content

View All
Trained, but Not Prepared: The State of Clinical Research Site Training

Trained, but Not Prepared: The State of Clinical Research Site Training

Sites complete every module and sign every attestation, and still end up learning your protocol through trial and error on real patients. This...

Posted by: Hope M , Director of Marketing Communications

ProofPilot ProofPilot
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.
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.
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
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
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.
Enrollment Plan Maturity Assessment

Enrollment Plan Maturity Assessment

Most enrollment plans are built once, hold a single number, and stay untouched until a milestone forces a reckoning. This nine-question...

Posted by: Hope M , Director of Marketing Communications

ProofPilot ProofPilot
On-Demand Webinar: Stop Guessing, Start Enrolling

On-Demand Webinar: Stop Guessing, Start Enrolling

The webinar explores the key limitations and downstream impacts of an oversimplified enrollment forecasting and tracking model. In conversation...

Posted by: Hope M , Director of Marketing Communications

ProofPilot ProofPilot
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
Case Study: A 730-Day Enrollment Window, Reshaped Before Day One

Case Study: A 730-Day Enrollment Window, Reshaped Before Day One

A top-10 pharma sponsor's aggressive Phase III cardiovascular timeline, modeled head-to-head against real-world data — surfacing a diversified...

Posted by: Hope M , Director of Marketing Communications

ProofPilot ProofPilot
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
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
New Treatments Hold Significant Promise, but are Marketing Teams Helping Life Sciences Companies Deliver on this Potential?

New Treatments Hold Significant Promise, but are Marketing Teams Helping Life Sciences Companies Deliver on this Potential?

Life sciences companies are operating in a new world, one where new treatments are being developed at breakneck speed, which holds unprecedented...

Posted by: Jennie R

PurpleLab PurpleLab
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
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
e-Labelling: The Road to Reduced Med Device Packaging

e-Labelling: The Road to Reduced Med Device Packaging

Regulators in the life sciences industry are making clear moves to connect patients, physicians and other stakeholders across the healthcare...

Posted by: Meghann H

Schlafender Hase Schlafender Hase
Canopy MLR Solutions

Canopy MLR Solutions

At Canopy, we provide best-in-class MLR Solutions. Our 360 suite of services covering MLR Operations, Regulatory AdPromo Review, Medical Review,...

Posted by: Andy S

Canopy Life Sciences Canopy Life Sciences
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
The Global Regulatory Intelligence Club for Pharmacovigilance

The Global Regulatory Intelligence Club for Pharmacovigilance

Read how Insife has created a unique service that can help pharma companies and biotechs, big and small, as well as CROs, by taking on the work...

Posted by: Natasa B

Insife Insife
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 , Director, Global Marketing

Qinecsa Solutions Qinecsa Solutions

Recommendations

ProofPilot
ProofPilot
“Amazing team facilitating site engagement tools for...”
Jose S
Jose S Principal
ProPharma
ProPharma
“One of the better medical information providers out...”
Joyce B
Joyce B UK/IE Pharmacovigilance Leader
PPD, part of Thermo Fisher Scientific
PPD, part of Thermo Fisher Scientific
“One of the best CROs I have worked with so far,...”
Jose S
Jose S Principal
See all recommendations →

PREMIUM LISTINGS

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