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SAS Clinical Data Management Online Training

Enroll for expert level Online SAS Clinical Data Management Training by Spiritsofts, Learn SAS Clinical Data Management Certification Training with Course Material, SAS CDM Tutorial Videos, Attend Demo for free & you will find Spiritsofts is the best Online Training Institute within reasonable fee.

Spiritsofts is the best Training Institutes to expand your skills and knowledge. We Provides the best learning Environment. Obtain all the training by our expert professionals which is having working experience from Top IT companies.

The Training in is every thing we explained based on real time scenarios, it works which we do in companies.

Experts Training sessions will absolutely help you to get in-depth knowledge on the subject.


Key FeaturesCourse ContentFAQs
  35 hours of Instructor Training Classes                            24/7 Support

 Lifetime Access to Recorded Sessions                              Practical Approach

 Real World use cases and Scenarios                                 Expert & Certified Trainers

Clinical Trails And Clinical Data Management
  • A clinical data management system or CDMS is a tool used in clinical research to manage the data of a clinical trial. In this module, you will learn Data management plan, Clinical data management process, Different types of phase trials and many more concepts.
  • Phase trails: preclinical 1,2,3 and 4
  • Drug discovery and development
  • Computer system validation
  • 21 CFR 11
  • CRF designing
  • Pharmacokinetics
  • Pharmacovigilance
  • Clinical data management process
  • CDISC introduction
  • CTM systems
  • Data management plan
Sub Chapter
  • This module gives you an description about Clinical Trail monitoring system, CRA, its responsibilites, How to monitor CRA, FDA guidelines, history and many more.
  • General abbreviated terms
  • Introduction to clinical trails
  • Responsibilities of CRA
  • Activities of CRA in house
  • CRA monitoring
  • Clinical trail monitoring
  • Responsibilities of PI
  • IRB
  • Informed consent form
  • ICH history
  • GPC guidelines
  • FDA history
  • FDA guidelines
  • IND
  • NDA reviews
  • Clinical research study document
  • CRF reviews and sample CRF’s
  • CRF data submission, CRF receiving
  • Introduction to SAS in CDM
Components Of SAS Different Data Types
  • Learn all about SAS different data types in this module of training.
  • Base/SAS
  • SAS/Graph
  • SAS procedures
  • SAS Macros
  • SAS (working with sql)
Open Clinical
  • By the end of this module, you will have a good understanding about Data base design, protocol planning and CRF data entry.
  • Data base design
  • Protocol planning
  • CRF Data entry
  • Data management
  • Study planning
  • Study design
  • Oracle clinical (overview)
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