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.
WHO ARE WE?
Phartrials is a company founded in 2005, specializing in pharmaceutical scientific consulting services with regulatory focus and monitoring in clinical research and relative bioavailability/bioequivalence (BA/BE) studies. Specialized in providing support to pharmaceutical companies in the registration and renewal of drugs, with up-to-date knowledge in line with current legislation and broad access to the database. It has expertise in the preparation of scientific technical reports (CTD format, bioequivalence protocols, scientific writing, DCDD, among others), as well as in the evaluation and monitoring of bioequivalence clinical studies. Working collaboratively, we help customers chart a clear course for each document.
The company was created to meet a need for the pharmaceutical market in issuing documents for registration and renewal of drugs in Brazil. Today, the company covers a larger area of services, advising the client within a scientific and regulatory approach and monitoring in pharmaceutical bioequivalence studies.
Phartrials has a Quality Management System duly implemented with a focus on the satisfaction of Customers with total commitment from Senior Management, in the constant search for continuous improvement of their activities and processes so that the quality standards of the services are maintained.
The company was created to meet a need for the pharmaceutical market in issuing documents for registration and renewal of drugs in Brazil. Today, the company covers a larger area of services, advising the client within a scientific and regulatory approach and monitoring in pharmaceutical bioequivalence studies.
Phartrials has a Quality Management System duly implemented with a focus on the satisfaction of Customers with total commitment from Senior Management, in the constant search for continuous improvement of their activities and processes so that the quality standards of the services are maintained.
Quality Policy
Phartrials provides excellent scientific and pharmaceutical services with appropriate regulatory compliance, aiming at customer satisfaction and committing to the development and qualification of its employees, as well as continuous improvement of processes.
Business
Pharmaceutical and regulatory scientific organization focused on drug research and development.
Mission
Support pharmaceutical companies on scientific and regulatory issues, contributing to the improvement of existing medicines and products in their portfolio, as well as new development and innovation projects.
Vision
To be a company recognized by the pharmaceutical market as a scientific and regulatory organization, providing safe and up-to-date technical support in the execution of projects, research, reports and monitoring in clinical trials.
Values
• ETHICS
• RESPONSIBILITY
• CONFIDENTIALITY
• RELIABILITY
• INTEGRITY
• RESPONSIBILITY
• CONFIDENTIALITY
• RELIABILITY
• INTEGRITY
Social and Environmental Responsibility Policy
Phartrials is a company that employs its 100% remote workforce, based in Goiânia – Goiás, with a team also in Campinas – São Paulo. Despite operating entirely remotely, we embed environmental, social and corporate governance into our values, acting as a responsible and proactive company. Our social and environmental responsibility policy is based on the pillars of Ecology, Economy, Society and Culture.
Our way of working eliminates the need for building heating, cooling and lighting, as well as the use of urban commuting pathways, contributing to the reduction of air pollutants and the generation of waste with great environmental impact, as well as saving resources and time. We deliver service excellence while promoting eco-consciousness on our team, encouraging an independent work model that improves employees’ living conditions and consequently their mental health.
Culturally, we nurture values that enrich society, respecting the culture and customs of employees and our Customers.
WHO ARE WE?
Phartrials is a company founded in 2005, specializing in pharmaceutical scientific consulting services with regulatory focus and monitoring in clinical research and relative bioavailability/bioequivalence (BA/BE) studies. Specialized in providing support to pharmaceutical companies in the registration and renewal of drugs, with up-to-date knowledge in line with current legislation and broad access to the database. It has expertise in the preparation of scientific technical reports (CTD format, bioequivalence protocols, scientific writing, DCDD, among others), as well as in the evaluation and monitoring of bioequivalence clinical studies. Working collaboratively, we help customers chart a clear course for each document.
The company was created to meet a need for the pharmaceutical market in issuing documents for registration and renewal of drugs in Brazil. Today, the company covers a larger area of services, advising the client within a scientific and regulatory approach and monitoring in pharmaceutical bioequivalence studies.
Phartrials has a Quality Management System duly implemented with a focus on the satisfaction of Customers with total commitment from Senior Management, in the constant search for continuous improvement of their activities and processes so that the quality standards of the services are maintained.
The company was created to meet a need for the pharmaceutical market in issuing documents for registration and renewal of drugs in Brazil. Today, the company covers a larger area of services, advising the client within a scientific and regulatory approach and monitoring in pharmaceutical bioequivalence studies.
Phartrials has a Quality Management System duly implemented with a focus on the satisfaction of Customers with total commitment from Senior Management, in the constant search for continuous improvement of their activities and processes so that the quality standards of the services are maintained.
Quality Policy
Phartrials provides excellent scientific and pharmaceutical services with appropriate regulatory compliance, aiming at customer satisfaction and committing to the development and qualification of its employees, as well as continuous improvement of processes.
Business
Pharmaceutical and regulatory scientific organization focused on drug research and development.
Mission
Support pharmaceutical companies on scientific and regulatory issues, contributing to the improvement of existing medicines and products in their portfolio, as well as new development and innovation projects.
Vision
To be a company recognized by the pharmaceutical market as a scientific and regulatory organization, providing safe and up-to-date technical support in the execution of projects, research, reports and monitoring in clinical trials.
Values
• ETHICS
• RESPONSIBILITY
• CONFIDENTIALITY
• RELIABILITY
• INTEGRITY
• RESPONSIBILITY
• CONFIDENTIALITY
• RELIABILITY
• INTEGRITY
Social and Environmental Responsibility Policy
Phartrials is a company that employs its 100% remote workforce, based in Goiânia – Goiás, with a team also in Campinas – São Paulo. Despite operating entirely remotely, we embed environmental, social and corporate governance into our values, acting as a responsible and proactive company. Our social and environmental responsibility policy is based on the pillars of Ecology, Economy, Society and Culture.
Our way of working eliminates the need for building heating, cooling and lighting, as well as the use of urban commuting pathways, contributing to the reduction of air pollutants and the generation of waste with great environmental impact, as well as saving resources and time. We deliver service excellence while promoting eco-consciousness on our team, encouraging an independent work model that improves employees’ living conditions and consequently their mental health.
Culturally, we nurture values that enrich society, respecting the culture and customs of employees and our Customers.
TEAM
Phartrials’ technical team is made up of highly qualified Associates, including PhDs, Masters and Specialists. In addition to their academic backgrounds and professional experiences, everyone has specific knowledge in Good Clinical Practice, with a certificate in ICH-GCP.Phartrials senior management is aligned with company processes and committed to achieving results and continuous improvement. The team is supported with the resources and means necessary to ensure the work meets the standards expected by customers.
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
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
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
AUDIT IN THE QUALITY MANAGEMENT SYSTEM
CONTACT