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FSP Global Clinical Supplies
PPD FSP global clinical supplies solutions help biotech, biopharmaceutical and medical device companies optimize clinical trial supplies lifecycle.
Regulatory Affairs for FSP
PPD FSP regulatory affairs solutions help navigate regulatory approval and market access with comprehensive end-to-end regulatory services.
Risk Management & REMS Strategies
Commitment to patient safety and compliance
Master Protocol Innovative Trial Designs
Download an Applied Clinical Trials article written by members of PPD’s Master Protocol Working Group.
UK Achieves Site Activation World Record for Roche During COVID-19 Pandemic
The UK’s Urgent Public Health response has been applauded by global life science company, Roche, as COVACTA, an international COVID-19 trial, closes to recruitment in nine countries.
European Union Clinical Trials Regulation: Clinical Trials Information System
PPD experts explain the key features of the Clinical Trials Information System (CTIS), which has been introduced alongside the new EU CTR.
FSP Quality Assurance
PPD FSP quality assurance solutions help biotech, biopharmaceutical and medical device companies to ensure the safety and integrity of clinical trials.