PRU/APIC was inspected by the Spanish authorities in May-2019
PRU/APIC has successfully passed the Spanish authorities inspection conducted in May-2019.
Bioanalytical services
Bioanalysis has contributed substantially to PRU/APIC leading position as an internationally recognized CRO
Our laboratories have the capability to develop and validate analytical methods for a variety of drug substances and metabolites using sophisticated high-throughput technologies. PRU/APIC utilizes a wide range of techniques available for bioanalysis, e.g., LC-MS/MS, LC-MS, and UPLC.
Clinical trials
Phase I - IV (Clinical Trials: Interventional and Observational Studies)
PRU/APIC provides client driven services through its experienced team of clinical research professionals by operating throughout many regions.
Country feasibility, site and investigator selections are crucial steps for any clinical trials, as it impacts the study for its whole duration, our culture and policy competent experts can help you walk through the markets forecasts safely.
Training
PRU/APIC offers Training Services for:
Bioequivalence studies BE/BA
(Bioequivalence/ Bioavailability/ Pharmacokinetics Studies)
PRU/APIC has its own accredited clinical units, comprising of the following:
Competitive study timeline
PRU/APIC professionals ensure the total elapsed time from protocol’s approval by the sponsor to the final approval from the JFDA/EC in three weeks. On Average the total study completion would require (2-3) Months.