Find vetted vendors, CROs, and technology partners

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

75

Resources

34

Categories

1054

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

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
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
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
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.
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
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
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
The Future of Systematic Literature Reviews

The Future of Systematic Literature Reviews

Introducing Literature Review by ReadCube Systematic Literature Reviews (SLRs) help researchers and organizations navigate the growing sea of...

Posted by: Meghann H

ReadCube ReadCube
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
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
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
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
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
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)
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
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
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 2: “Post-Marketing Safety Surveillance, EU & USA"

Series topic: Vigilance Medical Device Guidance Part 2: “Post-Marketing Safety Surveillance, EU & USA"

Join us for Part 2 of our webinar series on post-marketing safety surveillance, where we dive deeper into the intricate world of medical devices...

Posted by: Kalina S , test

Qinecsa Solutions Qinecsa Solutions
A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

A Business Case for a Document Comparison Software: The Best Insurance Policy for Regulatory Affairs

Intensifying regulatory requirements leave no room for error when putting goods into patients and consumers’ hands. Yet in life sciences, one of...

Posted by: Meghann H

Schlafender Hase Schlafender Hase

Recommendations

ProPharma
ProPharma
“One of the better medical information providers out...”
Joyce B
Joyce B UK/IE Pharmacovigilance Leader
Allucent
Allucent
“Helped me with very challenging clinical...”
Michael G
Michael G
EvidentIQ Group GmbH
EvidentIQ Group GmbH
“They were an excellent partner in the past”
Lars S
Lars S Chief of Staff
See all recommendations →

PREMIUM LISTINGS

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

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