We offer high quality front to end Clinical Research, Regulatory and Monitoring Services on time and under budget for local and international pharmaceutical companies.
Since 2009, a Full Service CRO with solid experience in all phases of Clinical Research, with dedicated attention to excellence, efficient communication and sponsor objectives, on time
and under budget
Our CRO also has solid experience in Phase I, Bioequivalence / Bioavailability and Early Phase Studies, Including First Time in Man, PK/PD, Food Effect and TQT Studies, audited and approved by FDA in June 2014.
In addition, we have full service experience in clinical and medical monitoring of pharmaceutical and device trials, senior project management, full regulatory and legal support, data management and statistics (EDC), quality assurance, medical safety and pharmacovigilance. These activities have been audited and validated with success by FDA in December 2019 for a trial conducted in Argentina.
Professional Service
Since 2009, Zenter Research has conducted many succesful clinical trials Phase II-III in most therapeutic areas.
Legal Representation and Liability before ANMAT for Sponsors Outside Argentina
Oxmox advised her not to do so, because there were thousands of bad Commas, wild Question Marks and devious.
Kolis Muller
Oxmox advised her not to do so, because there were thousands of bad Commas, wild Question Marks and devious.
Kolis Muller
Behind the word mountains, far from the countries Vokalia and Consonantia, there live the blind texts. Separated they live in Bookmarks grove right
Oxmox advised her not to do so, because there were thousands of bad Commas, wild Question Marks and devious.
Kolis Muller NY Citizen