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Get Brochure to Your MailAdvance Online Clinical Research Training Program
Clinical Research Online Training Program:
Clinical research is a branch of healthcare science that determines the safety and effectiveness (efficacy) 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 practice established treatments are used, while in clinical research evidence is collected to establish a treatment.
Clin Infotech 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. This Clin Infotech Clinical Research Program designed to provide total overview and skill globally in the field of clinical research. It would help professionals to upgrade & develop their knowledge about ICH GCP Guidelines, regulatory issues and other major aspects of clinical research & trial management.
Courses included in Advance Clinical Research Certification Program:
Clinical Data Management
Clinical data management is a highly specialized and exciting area in the pharmaceutical industry. Clinical research expertise is in short supply in this multibillion-dollar business. Clinical Data Management professionals are in high demand, and Clinical Research organizations are continually on the lookout for personnel with relevant experience. This broad and complex business provides outstanding job security and higher earnings.
Clinical data management is the process of collecting, filtering, and managing subject data in compliance with legal regulations. CDM processes' major purpose is to provide high-quality data while avoiding errors and missing data, as well as to collect as much data as possible for analysis. A CDMS or CTMS can be used to plan, report, and track internal activities. As a result, clinical research studies can obtain more effective, compliant, and fruitful data. These platforms are used by enterprises to collect, integrate, and validate data.
Pharmacovigilance:
Pharmacovigilance is a branch of medical science that involves a thorough examination and discussion of human health. It places a focus on disseminating restorative information by direct interaction with activists or through the collecting and study of blood, cells, apkins, or other examples. Clinical research is a scientific inquiry into the drawbacks, advantages, and issues of drugs or other therapeutic goods. As soon as you land a position in Pharmacovigilance, you should continue learning about new illnesses and how they affect people, as well as developing remedies and figuring out how to use pharmaceuticals to fight them.
Regulatory Affairs:
The regulatory affairs (RA) department of a pharmaceutical company is responsible for obtaining approval for new pharmaceutical products and ensuring that approval is maintained for as long as the company wants to keep the product on the market.
It serves as the interface between the regulatory authority and the project team, and is the channel of communication with the regulatory authority as the project proceeds. The RA department plays an important role in giving advice to the project team on how best to interpret the rules. During the development process sound working relations with authorities are essential, e.g. to discuss such issues as divergence from guidelines, the clinical study programme, and formulation development.
Medical Coding:
A medical coder translates details from a patient’s medical documents, such as physician's notes, lab reports, procedures, and diagnoses into universal medical codes to maintain accurate medical records. Healthcare providers and insurance companies use these standardized codes for billing and record-keeping.
A certified professional coder, in short CPC is responsible for overseeing the medical coding process. Medical coders make sure that the coding used is in compliance with all medical coding laws and regulations and also ensure that the coding aids reimbursable expenses when required.
Computer system Validation:
Validation of computerized systems is a documented process to ensure that a computerized system does exactly what it was designed to do in a consistent and reproducible way (suitability to use), ensuring the integrity and security of data processing, product quality, and complying with GxP applicable regulations.
The validation process begins with validation planning, system requirements definition, testing and verification activities, and validation reporting. The system lifecycle then enters the operational phase and continues until system retirement and retention of system data based on regulatory rules.
Software validation is the process of establishing documented evidence that confirms a computer system has been installed correctly, will meet users' needs and functions according to its intended use.
Statistical Analysis System (SAS)
Clinical SAS (Statistical Analysis System) is widely used software in the field of clinical research for analyzing and reporting clinical trial data. In India, there is a growing demand for professionals skilled in using SAS in the clinical research industry.
SAS (Statistical Analysis System) is a powerful software suite that is widely used in data management, analysis, and reporting. In the clinical and financial industries, SAS is a critical tool used for clinical trials, data management, financial modeling, and risk management. By taking a SAS clinical or SAS financial course training, you will gain a comprehensive understanding of SAS programming and its applications in these specialized fields. You will learn to manage and analyze large data sets, write programs to automate data processing, and generate reports to communicate findings to stakeholders.
Internship:
Our interns have the opportunity to gain work experience through internships with our clients on the in-house projects.
Clin Infotech provides high quality professional Internship in Clinical Research, Clinical Data Management, SAS, Pharmacovigilance, Regulatory affairs and Medical Coding. Training and projects are two best divisions of the company’s efforts to equip students to face industry needs.
The job oriented training program consists of three months of class room training and three months of internship in the different departments of the company. On successful completion of the internship, a certificate and a working experience letter will be provided.
Fresher’s can through this programme gain the opportunity to learn advanced skills with the added advantage of exposure to Industry databases and platforms with real time case scenarios
Clin Infotech Clinical Research Internship Program Advantage:
- Offer your learners a personalized, Clinical Software-based lab environment that enables your learners to learn With Hands on Experience on technology that is being skilled upon.
- Get hands-on experience with actual technology environments
- Up skill Our Trainees on the latest technologies and prepare them for Best Placements in the Top MNC’s
- Internship based “Suitability for Hire” after completion.
- Enhance your skills to transform from a novice to a “project –ready” candidate.
- Gain access to premium industry live projects.
- Live project work experience with exposure to industry SOPs & Client Communications.
Following Course Content for Clinical Research will be covered during the training:
Download the Syllabus - Blink
Eligibility Criteria:
Applicants are recommended to have one of the following life Science degrees: Bachelor’s, Master’s, or PhD, MBBS/ MD/B.D.S /M.D.S/ B.A.M.S / B.H.M.S /B.P.T/ B.Tech (Biotechnology / Pharmaceutical Science) / M.Tech (Biotechnology), B. Pharm /M.Pharm /BVSC / B.Sc. (Nursing) and all professionals working with Pharmaceutical companies, CROs and Hospital.
Clin Infotech Advantages:
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Online Clinical Research Placement Program:
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Through its comprehensive certification program, Clin Infotech offers thorough instruction in clinical research throughout the whole clinical trial process. With the help of this clinical trial management course, instructors will make sure that students have a procedural and administrative understanding of the clinical trial process as well as the capacity to advance their knowledge and abilities.
Enroll now!! Take advantage of this opportunity to engage with cutting-edge industry technologies and learn how to apply them in the domain of Clinical Trial Management.
certification:
Certificate will be provided for this Course on successful completion of Assignments & Projects.
Certificate would be awarded at the end of the program by Clin Infotech For Online Clincal Research Training Program. A fast track weekend course will also be conducted for employees & aspirants of Clinical Research Industry.
Our Placement Companies :
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