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Clinical Research

A Clinical Research Associate / Coordinator in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support the progress of clinical trials.

Clinical Research

A Clinical Research Associate / Coordinator in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support the progress of clinical trials.

Clinical Research

A Drug Safety / Pharmacovigilance Associate (DSA/ PVA) also know as Pharmacovigilance Officer, is a health science professional responsible for the monitoring, data collection and analysis of existing and new drugs…

Clinical Research

A Clinical Data Management specialist coordinates and manages data for clinical research studies. CDM specialist is responsible for clinical study databases and associated data.

Clinical Research

The Clinical Trial SAS Data Analysis and Reporting (CDAR) provides intensive learning on how SAS is used in clinical and pharmaceutical industries. In particular, how codes, analysis and reports are generated using SAS.

Clinical Research

A Drug Safety / Pharmacovigilance Associate (DSA/ PVA) also know as Pharmacovigilance Officer, is a health science professional responsible for the monitoring, data collection and analysis of existing and new drugs…

Clinical Research

A Clinical Data Management specialist coordinates and manages data for clinical research studies. CDM specialist is responsible for clinical study databases and associated data.

Clinical Research

The Clinical Trial SAS Data Analysis and Reporting (CDAR) provides intensive learning on how SAS is used in clinical and pharmaceutical industries. In particular, how codes, analysis and reports are generated using SAS.

Clinical Research

A Clinical Research Project / Study Manager(CRM) is responsible for the monitoring, data collection and analysis, and reporting of clinical trials performed and follow Ethical practices, ICH, GCP, and Clinical Safety guidelines per international markets.

Clinical Research

A Drug Safety-Pharmacovigilance Data and Safety Monitoring and report submissions to Authorities. Responsible for the monitoring,data collection and analysis,and reporting of drug safety information for compliance with drug safety regulations per international markets.

Clinical Research

Their primary role of a Drug Safety professional is to identify safety and risk information, evaluate and report with regulatory authorities. The training program provides in depth knowledge of roles and responsibilities of Drug Safety / Pharmacovigilance Specialist including theoretical aspect of the field and exposure to variety exercises based on industry requirements.

Clinical Research

This program is designed by industry experts for students and young professionals. The training provides in-depth knowledge of the roles and responsibilities of the Clinical Research / Clinical Study Manager, including the theoretical aspect of the field and exposure to variety exercises based on industry requirements.

Clinical Research

SAS program is the industry-standard statistical tool. QPDC offers Basic SAS Modules training program, which is designed to help interested candidates understand how SAS program manipulates and views data in various industries.

Clinical Research

SAS program is the industry-standard statistical tool. QPDC offers Advanced SAS Modules training program, which is designed to help interested candidates understand how SAS program manipulates and views data in various

SKILL-BASED-LESSONS

Certificate Program

Clinical Research Skill-Based-Lessons(CRSB) – Entry

This Lesson based programs is designed by industry experts for students and professionals. A Clinical Research Associate / Coordinator in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support progress of clinical trials. It contains 9 set of chapters.

Drug Safety Skill-Based-Lessons (DSSB) – Entry

This Lesson based program is designed by industry experts for students and professionals. A Drug Safety Data Management roles towards project Management and report submissions (DSA) is responsible for the monitoring, data collection and analysis, and reporting of drug safety information for compliance with drug safety. It contains 8 set of chapters.

SKILL-BASED-LESSONS

Clinical Research Skill-Based-Lessons(CRSB) – Entry

This Lesson based programs is designed by industry experts for students and professionals. A Clinical Research Associate / Coordinator in House is a professional employed by a pharmaceutical, medical device manufacturing, or clinical research organization (CRO) to support progress of clinical trials. It contains 9 set of chapters.

Drug Safety Skill-Based-Lessons (DSSB) – Entry

This Lesson based program is designed by industry experts for students and professionals. A Drug Safety Data Management roles towards project Management and report submissions (DSA) is responsible for the monitoring, data collection and analysis, and reporting of drug safety information for compliance with drug safety. It contains 8 set of chapters.