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Clinical Research is a most knowledge-intensive and interesting field in the pharmaceutical industry. There are more than 2, 50,000 positions unemployed in global Pharmaceutical industry.
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Difference Between Clinical Research And ClinicalData Management Introduction to ClinicalResearch Clinical Research is a most knowledge intensive and interesting field in pharmaceutical industry. The billion dollar industry is demanding the employment opportunities of qualified and trained professionals in clinical researchsector. What is clinical research? Clinical research is a branch of healthcare 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 from clinical practice. In clinical research evidence is collected to establish a treatment for particular disease. Clinical research aims to advance medical knowledge by studying people, either through direct interaction or through the collection and analysis of blood, tissues, or othersamples Types of Clinical Research The clinical research is categorized into two typesmainly Comparative Clinical Research It is also known as controlled clinical trial. The research participants are divided into two group’s one group receives the investigational treatment, while another group either records the conventional (traditional) treatment or nothing. The control group might be given a fake treatment. This is an idle pill, injection or implantation that seems similar to the investigationaltreatment. The treatment conducted is kept confidential that means patient and physician both are unaware that who is acquiring the investigationaltreatment. Open Label Clinical Research In this type the patient and physician both know that the investigational treatment is going to conduct. Phases of Clinical ResearchTrial There are main phases of clinical trials: Phase I, Phase II, Phase III andPhase IV. The four phases of the drug approval process are separate clinical trials, and the entire process typically takes eight to 10years. Phase I
In this phase the first drug treatment is carried out on a small group of people. Investigator or a scientist figure out the drug’s safety, determine a safe dosage range and analyze its sideeffects. • Phase II • In phase II same procedure is followed as phase one but the treatment is carried out for the large number of people to observe its behavior andsafety. • Phase III • The drug treatment is conducted for larger group of people. In this phase scientists or observer confirms effectiveness of a drug on particular disease, monitors its side effects, compare with traditional treatments and gathers all the information about the experiment so that the drug is been used safely in future. • Phase IV • Phase four deals with the post marketing studies that are conducted after a treatment will be approved for commercial use by FDA. Post marketing study includes all the required information about the drug along with its hazards, profits and best usage. • Clinical Data Management (CDM)System • Clinical Data Managementis a system or a tool that includes overall data generated in clinical trials of particular medicine. CDM is collection, integration, validation of clinical trial data. In clinical trial investigators collect data on patient’s response to particular drug for a defined period. This data is then forwarded to the sponsor to analyze it using statisticalanalysis. • Types of Clinical Data • Clinical data is a staple resource for most health and medical research. Clinical data is either collected during the course of ongoing patient care or as part of a formal clinical trial program. Clinical data management system falls into followingtypes • Electronic health records • Administrativedata • Claims data • Let us discuss them one byone • Electronic healthrecords
It is type of clinical data obtained at hospitals, health care centers, or in clinics. The data can be prescription of drugs, laboratory tests, psychological monitoring data, diagnosis, treatment and patients insurance. It is also referred as the electronic medical record-EMR of clinical data management system; it is not available for outsideresearchers. • Administrative Data • Administrative data is often with electronic health record, and these are non- clinical research data focused on record-keeping surrounding a service, such as hospital discharge information. • ClaimsData • As the name resembles it includes data regarding insurance claim. It includes billable interactions between the patients and insurance company. This data is again subdivided into four general categories as inpatient, outpatient, pharmacy andenrollment. • Steps of Clinical Data • Clinical datacollection is very challenging and innovative task in clinical research. The clinical data generates at various stages and its maintenance is becoming a crucial task for Clinical data management professional’s clinical data is generated at various stages from its designing topresentation. • The clinical data is generated at followingstages • DataDesign • Datacollection • DataEntry • dataValidation • DataCleanup • DataAnalysis • Data Reporting • DataPresentation.