You keep customers by delivering on your promises, fulfilling your commitments and continually investing in the quality of your relationships.- Brian Tracy
Home
About Us
Services
Training
OppOrtunities
Contact Us
 
Training

 

 
PHARMACOVIGILANCE
Clinical Data Management
SAS-SDTM MAppings
MEDICAL CODING

 

 
For Registrations, please Send Mail to
mokshabio@yahoo.com
info@mokshabio.com
Phone: 9959861177
 

 

 .

Our Training Division, Moksha Institute of Corporate Training (MICT), is Offering Corporate Training for Industrial people and Job Oriented Training for Academic Students in Clinical Development Program.
PHARMACOVIGILANCE
 
  • PHARMACOVIGILANCE PROCESS
 
  • PHARMACOVIGILANCE REGULATIONS
 
  • DIFFERENT TYPES OF SAFETY REPORTS
 
  • PSUR AND ITS SUBMISSION TIMELINES
 
  • SCOPE OF THE PHARMACOVIGILANCE
 
  • REGULATORY REPORTS
 
  • PERIODIC REPORTS (PSUR)
 
  • AGGREGATE REPORTS (LINE LISTING)
 
  • CASE PROCESSING TRAINING
 
  • DATA COLLECTION & PROCESSING
  CLINICAL DATA MANAGEMENT
 
  • Protocols and CRF Design
 
  • Data management Plan
 
  • Good Clinical Practice & Other Regulatory Guidelines
 
  • Data Capture Methods and Data Entry
 
  • External Data Loading And Data Validation
 
  • Statistical Analysis & Reporting
 
  • Regulations & Guidelines for CDM
 
  • Pharmacovigilance, MedDRA
 
  • EDC (Electronic Data Capture.)
 
  • Management of ADR.
 
  • OpenClinica.
 
  • Oracle Clinical (overview)
 
  SAS-SDTM Mapping
 
  • introduction PROC CDISC
 
  • Fundamentals of the SDTM.
 
  • Datasets AND Domains.
 
  • SDTM Standard Domain Models.
 
  • Submitting Data in Standard Format.
 
  • Models for Special-Purpose Domains
 
  • Domain Models for General Observation Classes
 
  • USING THE CDISC Domain Models,
 
  MEDICAL CODING
 
  • ICD-9-CM Coding and Structure
 
  • ICD-9-CM Coding Practice Problems
 
  • Current Procedural Terminology(CPT)
 
  • 3D-QSAR
 
  • Reimbursement
 
  • CPT Coding Practice Problems
 
 
 
 
 
 
 
 
 
 
 
 
All rights reserved @ 2010 Moksha Bio Sciences