Website : http://www.todaycourses.com SAS CDM Online Training Concepts : Clinical Trails and Clinical Data Management : Phase trails: preclinical1,2,3 and 4 Drug discovery and development ICH GCP Computer system validation 21 CFR 11 CRF designing Pharmacokinetics Pharmacovigilance Clinical data management process CDISC introduction CTM systems Data management plan Sub Chapter 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 Base/SAS SAS/STAT SAS/Graph SAS/ACCESS SAS procedures SAS Procedures SAS Macros SAS (working with sql) Open clinical Data base design Protocol planning CRF Data entry Data management Study planning Study design Oracle clinical (overview) sas cdm training, certified sas course, online sas cdm training, sas cdm online, online sas cdm classes, sas cdm training online, sas cdm training hyderabad, sas clinical online training, sas certification, sas classroom training, clinical sas training, online sas training, onlinetraining sas, online sas training india, sas statistical, sas online training experience, training online sas, statistical analysis, training sas clinical online, clinical sas course, clinical trial data analysis, graphical analysis

1. L/O/G/O
SAS CDM Online Training
http://www.todaycourses.com

2. Clinical Trails and Clinical Data
Management
 Phase trails: preclinical1,2,3 and 4
 Drug discovery and development
 ICH GCP
 Computer system validation
 21 CFR 11
 CRF designing
 Pharmacokinetics
 Pharmacovigilance
 Clinical data management process
 CDISC introduction
 CTM systems
 Data management plan

3. Sub Chapter
 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

4. Sub Chapter
 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

5. Components of SAS Different
data types
 Base/SAS
 SAS/STAT
 SAS/Graph
 SAS/ACCESS
 SAS procedures
 SAS Procedures
 SAS Macros
 SAS (working with sql)

6. Open clinical
 Data base design
 Protocol planning
 CRF Data entry
 Data management
 Study planning
 Study design
 Oracle clinical (overview)

7. L/O/G/O
Thank You!