REFERENCE IN THE PHARMACEUTICAL MARKET

IN CLINICAL TRIAL MONITORING AND TECHNICAL-SCIENTIFIC DOCUMENTATION, MEETING REGULATORY REQUIREMENTS WITH HIGHLY SPECIALIZED STAFF.

Phartrials has a team of doctors, masters and experts in the field of pharmaceutical and health sciences, with extensive experience in regulatory affairs, research and clinical studies. We provide secure, complete and accurate information through a comprehensive technical-scientific database, optimizing operational efficiency. We keep up-to-date on new resolutions, standards and guidelines from Regulators, both domestic and international. Thus, we guarantee excellence in customer service, with the commitment of individualized attention according to the demands of the pharmaceutical market.

SERVICES

MONITORING IN
CLINICAL TRIALS

PREPARATION OF TECHNICAL-SCIENTIFIC DOCUMENTATION AND/OR EVALUATION TO COMPLY WITH REGULATORY STANDARDS

AUDIT FOR QUALIFICATION OF PHARMACEUTICAL BIOEQUIVALENCE CENTER

AUDIT FOR QUALIFICATION OF PHARMACEUTICAL EQUIVALENCE CENTER (EQFAR)

SERVICES

MONITORING IN
CLINICAL TRIALS

PREPARATION OF TECHNICAL-SCIENTIFIC DOCUMENTATION AND/OR EVALUATION TO COMPLY WITH REGULATORY STANDARDS

AUDIT FOR QUALIFICATION OF PHARMACEUTICAL BIOEQUIVALENCE CENTER

AUDIT FOR QUALIFICATION OF PHARMACEUTICAL EQUIVALENCE CENTER (EQFAR)

SATISFIED CUSTOMERS

SATISFIED CUSTOMERS



Contact us for more information or if you still have any questions.

Avenida Anhanguera, qd. 38 lt. 96, Nº 4803, Sala 1404, Ed. Rita de Albuquerque, Setor Central, Goiânia-GO, CEP: 740430-11
COMPANY - WHO WE ARE?

QUALITY POLICY

MISSION

VISION

VALUES

SOCIAL AND ENVIRONMENTAL RESPONSABILITY POLICY

TEAM
OUR SERVICES

WE SPEAK SCIENCE!

MONITORING IN CLINICAL TRIALS

PREPARATION OF THECNICAL-SCIENTIFIC DOCUMENTATION AND/OR EVOLUATION TO COMPLY WHITH REGULATORY STANDARTS

AUDIT FOR QUALIFICATION OF PHARMACEUTICAL BIOEQUIVALENCE CENTER
AUDIT FOR QUALIFICATION OF PHARMACEUTICAL EQUIVALENCE CENTER (EQFAR)

AUDIT IN THE QUALITY MANAGEMENT SYSTEM

CONTACT