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Inside Cliniminds


Our Pharmacovigilance Training
Partner
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Bangalore Enquiry Form
Cliniminds Programs are Certified & Accredited by
Pharmaceutical Society of India
Advanced Post Graduate Diploma in Clinical Research & Pharmacovigilance
/
Advanced Post Graduate Diploma in Clinical Research & Regulatory Affairs in Pharma & Clinical Research
/
Advanced Post Graduate Diploma in Clinical Research & Clinical Data Management & Biostatistics + SAS
6 Months Part Time Class Room Program + One month Project @ Bangalore
Call : +91-9663691388
Email : anil@cliniminds.com bangalore@cliniminds.com
Website:www.cliniminds.com

Why Clinical Research..

  • Wide Job Horizon
  • Attractive Salaries
  • Higher Professional Growth
  • Global jobs & Training Opportunities
  • Higher Job Satisfication
  • Need of more than 50,000 trained clinical Research professionals by 2012 (McKinsey)

Why Cliniminds..

  • Industry recognized courses
  • Practical oriented Classes
  • Industry experienced faculties
  • Video conferencing sessions
  • Campus interviews

Key Employers..

  • Max Neeman International
  • Dabur
  • CliniRx
  • Ranbaxy
  • Excel Life Sciences
  • Pfizer
  • Acccenture
  • TCS
  • Wipro
  • Clinsys
  • Fortis
  • Novartis & Many More other Companies…..

Clinical Research

Drug discovery & development Ethical Considerations Clinical Trial Regualtions Clinical Trial Planning & Management
Submissions & Approvals Study Start Up Process Monitoring Essentials QA & QC Special Clinical Trials
Practiacal case scenarios Role plays Hands on training

Pharmacovigilance(Option 1)

  • Overview of Pharmacovigilance
  • MedDRA
  • Diagnosis And Management of ADR
  • Medical Evaluation of Adverse Events
  • Expedited Reporting Requirements
  • PSURs
  • PV Database & Signal Detection Tools
  • Risk assessment management
  • Exposure to Pharmacovigilance Softwares

Pharma Regulatory Affairs(option 2)

  • Pharma Regulatory Practices
  • Import and Export of Drugs
  • GMP
  • QA and Regulations
  • Regulations Governing Clinical Trials
  • Drug Policies in India
  • Orphan Drugs
  • Regulations in Pharmaceutical Devices
  • TRIPS and Pharma Industry
  • IPR Management
  • Patent Application

CDM & Biostat/SAS (Option 3)

  • Overview of Data Management
  • Study Set Up
  • CRF Design Considerations
  • Data Entry,Remote Data Entry
  • Identifying and Managing Discrepancies
  • Medical Coding
  • Database Closure
  • Electronic Data Capture
  • Tracking CRF Data
  • Managing Lab Data
  • Collecting AE Data
  • Creating Reports and Transferring Data
  • Enterprise CDM Tools
  • Basics of Biostatistics
  • Sample Size Calculation
  • Statistical Analysis Plan
  • Para / Non-Parametric Tests
  • Orientation to SAS Softwares
Name Ph.No.
EMail Branch
Fill the form,
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No.420, 9th Main, Banashankari 2nd Stage,Bangalore - 560 070
Mobile: +91-9663691388
Tel: :+91-80-41624204
Email : anil@cliniminds.com bangalore@cliniminds.com
Website: www.cliniminds.com
Fee for the Program is Rs.100,000 including Laptop with online E-Learning System.Those who do not need Laptop, fee would be Rs.80,000 payable in 2 instalments.Fee for the Advance Post Graduate Diploma in Clinical Research & Clinical Data Management+SAS is Rs. 130,000(Including Laptop). Limited seats available..Admissions ongoing.
For free prospectus contact
Mobile: +91-9447765327,+91-9656154115
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