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Here are five questions to ask yourself to assess the value of your contract research organization (CRO) during a recession.

Kirsten Messmer, Ph.D., R.A.C., principal regulatory affairs specialist, details changes in regulatory guidelines for first-in-human trials.

Special populations, like children and the elderly, require nuanced considerations in vaccine development.

Despite a CRA talent shortage, we have created a deep bench of CRAs to ensure our clients’ studies are well-staffed. Here’s how.

Explore the significance of regulatory compliance in healthcare, its impact on patient safety and data integrity. Learn about key requirements, challenges, and strategies.

PPD’s dedicated government and public health services group has successfully delivered clinical research services to various agencies, contractors and nonprofits in both prime contractor and subcontractor capacities within full compliance of all federal contracting requirements for nearly 30 years.

PPD has developed a novel approach to accessing sites and patients.

Explore FSP rebadging to address staffing challenges amid business disruptions in a way that mutually benefits both your business and your employees.