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Phase I services

Decades of experience in conducting Phase I clinical trials

With participants safety paramount, PAREXEL Early Phase has developed a superior range of services for the conduct of first-in-man - or first-in-human (FiH) - and other Phase I safety studies giving you the assurance that your compund will move into human testing swiftly and safely.

Many of our units are based directly within hospitals providing direct emergency room access to offer you the best possible environment for the performance of first-in-human and other Phase I safety studies. Additionally, all of our units have well documented emergency procedures, a high ratio of medical doctors to beds and highly experienced nursing teams. With over 30 years experience in performing Phase I trials, we provide our clients with the clinical pharmacology, scientific and clinical expertise that they need - practical advice, sound protocol design, quality data and the assurance of the smoothest possible transition into the clinical phase of development.

Phase I services include:

  • Full scope of Phase I clinical services
  • Combination protocols
  • Clinical pharmacology consulting
  • Safety studies in target patient populations
  • Comprehensive clinical data science services

About PAREXEL Early Phase

With a full scope of services from First in Man through Proof of Concept, PAREXEL Early Phase has a global network of clinical units that test compounds and devices in healthy volunteers and patients, helping our biopharmaceutical clients make valuable decisions quickly and safely.