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PPD In The News

The Changing Role of the CRO and its Effect on Project Management

Volker Hack and Denise Sackner write about the impact of increased clinical trial complexity on project management.

Applied Clinical Trials  (June 2017)

PPD expands Virginia vaccine lab with an eye on assays

A report on the expansion of the PPD® Laboratories vaccine sciences lab in Richmond, Virginia, as reported in Outsourcing-Pharma.

Outsourcing Pharma  (May 2017)

Acurian: new consulting service provides ‘continuum of support’

Outsourcing-Pharma reports on the introduction of Acurian Consulting Services.

Outsourcing Pharma  (May 2017)

Movement for real-world evidence as PPD and Evidera launch new research unit

CenterWatch reports on the combining of PPD’s medical affairs operations team and Evidera.

CenterWatch Weekly  (May 2017)

PPD combines medical affairs team with real-world research subsidiary Evidera

FierceBiotech reports on combination of PPD’s medical affairs research operations and Evidera.

FierceBiotech  (May 2017)

PPD forms new unit with Evidera, MARO teams

Outsourcing-Pharma reports on combination of PPD’s medical affairs research operations and Evidera.

Outsourcing Pharma  (May 2017)

Solid-Phase Extraction for the Preparation of Aqueous Sample Matrices for Gas Chromatographic Analysis in Extractable/Leachable Studies

Steve Zdravkovic outlines the attributes of solid phase extraction and the advantages it offers compared to liquid/liquid extraction.

Pharmaceutical Technology  (May 2017)

Quality Certificates for Small Molecule Drug Product Applications for International Regulatory Submissions

In this article, Monika Jain discusses the issues regulatory professionals may encounter while arranging for a variety of certificates for applications for small molecule drug products.

Regulatory Focus  (May 2017)

CROs and Next-Gen Drug Development

PPD's David Johnston comments on the new operational, organizational and partnership-based approaches to drug development.

Contract Pharma  (May 2017)

Leveraging Next-Gen FSP Models to Better Manage Post-approval Regulatory Workloads

Elizabeth Madichie, Alistair Davidson, Denise Moody and Vincenzo Cannizzaro explain how a one-team model forges an outsourcing partnership to deliver efficient global regulatory lifecycle management.

Contract Pharma  (May 2017)

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