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Hundreds of
Diligent Qualified Providers at your fingertips
Vendor qualification needed an upgrade.
Diligent Pharma is the industry’s leading vendor qualification ecosystem, connecting pharma and biotech Sponsors to a global network of Diligent Qualified GCP and GCLP Providers.
Accelerate study launch with direct access to high-quality qualification questionnaires and audit reports.
The industry’s essential process innovation
Pharma and biotech organizations often qualify the same Vendors with different tools and criteria. Every year, more than $3 billion and 17 million days are wasted on redundant qualification activities.
The solution? Audit modernization.
Our FDA-accepted process innovation accelerates the vendor qualification and onboarding process, allowing clinical trials to start on time. This centralized approach drives efficiency without compromising compliance rigor, data integrity, or quality.
Rigorous compliance
Improve risk awareness and compliance with a comprehensive global qualification model
- Assess providers against rigorous standards established in a collaborative model with hundreds of pharma, biotech, and regulatory leaders
- Drive efficiency without compromising on quality via a centralized source of qualification data mapped to the latest global regulatory requirements
- Pair up with an industry auditor with over ten years of experience in GCP or GCLP, matching your specific requirements to their subject matter expertise
Rapid vendor qualification
Expedite the audit process with direct access to up-to-date vendor qualification information
- Shorten your vendor qualification timeline from over three months to less than a week or even a day
- Streamline partner discovery in your next trial with our vendor network, covering specialties to full-service, even including emerging categories like eClinical technologies and services
- Join a pre-scheduled vendor qualification audit, confidential and custom-fit to your desired scope
Cost-efficient risk management
Lower costs and enhance risk management through data-driven decision making
- Qualify vendors while minimizing direct and indirect expenses by 60%
- Eliminate the significant opportunity cost of study start-up delays
- Choose the right vendor with strategic, data-backed, risk-based decision making across nearly thirty clinical trial service categories
>1000+
successful qualification exchanges
>90
avg. days saved per qualification
>60%
cost reduction per qualification
How is leveraging centralized qualification data a credible and acceptable way to qualify Vendors?
ICH Q9, ICH Q10, and ICH E6(R3) leave the qualification method up to trial Sponsors, and the industry has long relied on independent auditors to qualify the same Vendors. Diligent is simply allowing multiple Sponsors to benefit from a single qualification, eliminating the redundancy of every Sponsor conducting similar qualification assessments.
The FDA has reviewed Diligent’s model and accepts pharma and biotech’s secure reuse of centralized qualification data as a compliant way to qualify Vendors.
Questions? Let’s chat.
Schedule a one-on-one with our team to learn more about how Diligent can support your unique qualification and risk management needs.