Find vetted vendors, CROs, and technology partners

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

75

Resources

34

Categories

1102

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
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
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
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
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.
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.
(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.
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
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
(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.
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
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
How AI Can Drive Smarter, Faster Pharmaceutical Workflows

How AI Can Drive Smarter, Faster Pharmaceutical Workflows

The pharmaceutical industry is evolving rapidly, but inefficient research workflows can slow innovation. With scientific literature growing...

Posted by: Katherine A , Product Marketing Manager

ReadCube ReadCube
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
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
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
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
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
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
The Last Mile of Patient Recruitment Social

The Last Mile of Patient Recruitment Social

If you're doing all the right recruitment outreach but your pre-qualified referrals are falling into a black hole and not converting into...

Posted by: Colleen Y , Head of Marketing

ProofPilot ProofPilot

Recommendations

ProPharma
ProPharma
“One of the better medical information providers out...”
Joyce B
Joyce B UK/IE Pharmacovigilance Leader
StudyKik
StudyKik
“Innovative solutions to support enrollment and...”
GINA W
GINA W
Copyright Clearence Center (CCC)
Copyright Clearence Center (CCC)
“CCC provides complete literature/reference access,...”
KK H
KK H
See all recommendations →

PREMIUM LISTINGS

Clinical writing and development solution for today's needsSynterex is a global clinical and...
Empowering Global Pharmaceutical Success Through Innovative Consultancy Solutions This company...
About CompanyAlphaLife Sciences is an AI-first platform company transforming how novel therapies...
Berry Consultants is a statistical consulting company specializing in innovative clinical trial...
Redefining Health Care for the Modern WorldEvernorth brings the power of innovation and...
Alphanumeric provides a bridge between pharmaceutical companies and HCPs, patients, and...
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...
In the rapidly evolving landscape of drug development, Weave stands at the forefront with its...
Clarivate is a leading global provider of transformative intelligence. We offer enriched data,...
Revolutionizing Clinical Trial Transparency and ComplianceTrialAssure is the global leader in...
Elevate Your Drug Information Accuracy with Premier Regulatory Excellence This company stands at...
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...
Pioneering Excellence in Drug Safety and Healthcare SolutionsWe are a trusted partner to the...
Schlafender Hase delivers an easy-to-use document comparison software for regulated industries to...
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...
Qinecsa Solutions is a reliable international collaborator uniting top-notch technology 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...
Streamline Your Research WorkflowWith ReadCube's literature management system, your...

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