Clinical Research Courses

GIHS have grip in more than 6 different Clinical Research Programs which are internationally designed and fulfilled as per the need. Through our programs professionals & students can have recent updates on various branches of clinical research programs. Clinical research is a branch of medical science that determines the safety and effectiveness of medications, devices, diagnostic products and treatment regimens intended for human use. These may be used for prevention, treatment, diagnosis or for relieving symptoms of a disease. Clinical Research is different than clinical practice. In clinical practice, one used established treatments while in clinical research evidence is collected to establish a treatment. The term clinical research refers to the entire bibliography of a drug/device/biologic, in fact any test article from its inception in the lab to its introduction to the consumer market and beyond. Once the promising candidate or the molecule is identified in the lab, it is subjected to pre-clinical studies or animal studies where different aspects of the test article (including its safety toxicity if applicable and efficacy, if possible at this early stage) are studied. Since Few years clinical research sector is growing tremendously and today it is a 50 million US dollar Industry. GIHS have the quality to deliver the best update and education of Clinical Research.

Courses

GIHS provide the wide range of professional Certification courses, cost effective, job oriented programs in clinical research. These programs can be distance learning/online. We provide online clinical research programs and data management certificate course and Pharmacovigilance trials. These includes the master of clinical research courses online, diploma or postgraduate in clinical trials short courses, clinical trials certificate courses, Pharmacovigilance certificate courses and SAS certification courses. Our courses are design considering the syllabus with attractive fees structure.

Clinical Research & Quality Assurance GCP Audits / Inspections

This program has been conceptually designed to meet the demand in industry for CR and QA professionals with understanding of clinical quality assurance training with respect to the regulatory requirements. It introduces you to conduct clinical trials and to important quality assurance methods, processes and practices.
Clinical Data Management & SAS – Statistical Analytical System

This program is combination of clinical data management and SAS is a comprehensive training course intended to deliver the understanding of data management and analysis of the data collected.
Pharmacovigilance & Medical/Scientific Writings

This program is especially designed to understand the regulatory guidelines in terms of collecting the post market safety data collection of pharmaceutical drug/device. Medical writing includes writing of documents related to and drug development / clinical research.
Regulatory affairs & IPR Patents

This program is designed to provide the fundamental to clinical research is the domain of regulatory affairs which forms a network of standardized laws, regulations and guidelines creating an equilibrium between facilitation of innovation and safety of subjects enrolled in clinical trials.
Clinical Research & Pharmacovigilance

This program is designed to provide in-depth understanding of the basic principles of Clinical Research and pharmacovigilance both domestically and internationally.
Clinical Trials Management

The Clinical Trials Management program will update you to master the clinical trials process and requirements to standard practice and regulatory requirements.