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PPD Post-Approval Services

Wilmington, United States

Contact Details

929 North Front Street

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Phone number: +1 303 683 9961
Web address:
Email address: Craig.Eslinger@

Company Profile

Ensure the commercial success of your product and fulfill regulatory commitments with PPD, a partner you can trust to provide an integrated suite of post-approval services. Utilizing a dedicated staff of experts and processes tailored for the unique needs of post-approval programs, PPD can help shape a product’s success, maximize value at product launch and support the product throughout its lifecycle. We can help design and implement successful programs that are fully compliant with all global regulatory requirements. And, with our innovative technology, flexible staffing and extensive suite of post-approval services, we deliver the best in quality while providing operational efficiencies to help our clients meet their commercial objectives.

Medical Communications
PPD’s global medical communications team provides flexible, integrated, multi-channel contact center services such as:
• Medical information
• Adverse event and product complaint documentation
• Patient education and adherence
• REMS customer interactions
• Clinical trial screening

Medical Writing
PPD offers a wide array of medical writing services to support post-approval and medical information,including:
• Standard response documents
• Escalated inquiry management
• Biomedical literature reviews
• AMCP dossiers
• Slide decks, manuscripts and white papers
• Editorial review

Status: Privately held
Date established: 1985
Number of local staff: 1000
Additional services

We offer a wide range of services, including:
• Medical information and professional contact center services
• Medical writing and editorial services
• Product safety and pharmacovigilance
• Risk management/REMS programs
• Link to a full suite of post-approval services within PPD, such as epidemiology, health economics and outcomes research, registries, and observational studies


PPD has the expertise and experience necessary to meet the needs of our clients, including the following:
• Totally integrated suite focused on commercial success that can work independently or in concert with your current providers or internal resources
• 20+ year history focused exclusively on post-approval
• Highly experienced and professional team of experts
• Ability to leverage PPD’s clinical expertise to link closely with R&D to begin building the commercial message early
• Full-service or standalone support
• Global footprint with offices in 46 countries
and more than 12,500 employees worldwide

Key Contacts

Director, Business Development
Director, Business Development
Global Head, Business Development
Pharm.D., Vice President, Medical Communications
M.D., Senior Vice President, Pharmacovigilance
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