Clinical Data Management Course Training Kukatpally Ameerpet Hyderabad India

Best Clinical Data Management Training in Hyderabad

Clinical Data Management Training in Hyderabad is one of the Critical and important phases during all Clinical Research Trial Phases. Using specific Clinical Data Management techniques- Data collected during the clinical trial will be purified, cleaned and statistically high-quality standards data is prepared. Any drug/device development process needs such data management techniques to produce exact and consistently good in quality life-saving molecules and medical equipment.

Clinical data management (CDM) is a process in clinical research, where it leads to the generation of high-quality, consistently good in quality and according to statistics sound data from clinical trials.

Clinical data management plays a great important role in the data collection phase of clinical research and it is the process of collecting and managing research data is done in fixing with regulatory standards to obtain quality information that is complete and free from error.

Clinical Data Management Course in Hyderabad ensured with collection, integration, and obtained of clinical data at a proper quality and it also supports to conduct, manage and detailed structure of studies across the spectrum of clinical research.

The field of clinical data management (CDM) has come about due to the requirement from both  relating to medicinal drugs industry and the regulatory authorities for the development of medicinal products continues to accelerate, regulatory entities by requiring quality-assurance standards to be met in collecting the data used in the drug evaluation process. Such standards are created by the Clinical Data Interchange Standards Consortium (CDISC), are particularly vital to CDM, the Study Data Tabulation Model Implementation Guide for Human Clinical Trials (SDTMIG) and the Clinical Data Acquisition Standards Harmonization (CDASH).

The former one is currently mandated for use by the U.S. The Food and Drug Administration (FDA) and the latter created a standard format for collecting data across studies so that data submissions can be more easily tracked and reviewed.Specialized tools are used in CDM to create audit trails that allow the illogical or surprising lack of compatibility should be minimized even in large and complex clinical trials. Clinical data management systems (CDMS) are especially absolutely necessary in clinical trials conducted across medical centers in which a huge amount of data is produced. Some of the examples are Oracle Clinical, rave, eClinical suite, Clintrial, and Macro. The clinical data manager plays a key role in the setup and conduction of a clinical trial where the data collected during a clinical trial forms the basis of subsequent safety and efficacy. The analysis which in turn leads to decision making on product development. The clinical data manager is also involved in early discussions about data collection sources and  in foreign country the development of data collection tools based on the clinical trial protocol. The computer systems used in the processing and management of clinical trial output data must undergo validation to ensure that they perform as intended and that results are reproducible.

Clinical Data Management Training in Hyderabad involves various activities like:

  1. Data Collection
  2. Case Report Form (CRF) designing
  3. CRF Tracking
  4. CRF Annotation
  5. Database Design
  6. Data Entry
  7. Medical Coding
  8. Data Validation
  9. Discrepancy management
  10. Database Lock

ICRDM Training Highlights:-

  • Get Training from India’s  foremost training Institute in Clinical Research
  • Job-oriented Specialised training
  • Hand on training with guidance expert trainer.
  • Curriculum was designed as per the requirements of an industry.
  • Career counseling and resume preparation will be done the help of experts.
  • Case studies based teaching.
  • Excellent career opportunity in Pharmacovigilance.
  • Internship in the best Companies/hospitals across Bangalore.
  • Frequent increments and opportunities of traveling abroad while working with MNCs.

Eligibility Qualification:-

  •  B.Sc / M.Sc in Biotechnology
  •  B.Sc / M.Sc in Microbiology
  •  B.Sc / M.Sc in Genetics
  •  B.Sc / M.Sc in Biochemistry
  •  B.Sc / M.Sc in Life Sciences
  •  M.B.B.S / B.D.S / B.A.M.S / B.H.M.S
  •  B.Pharmacy / M.Pharmacy
  •  Pharm.D
  •  Graduates or Post Graduates in Nursing
  •  B.E (BT) / B.Tech (BT)
  •  Ph.D in Life Sciences / Biomedical Science

Along With Clinical, we have also started various courses like Pharmacovigilance Training, Clinical Data Management Training, Clinical Research Training, Data Science Training, Regulatory Affairs Training, in Kukatpally at Hyderabad, India