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EDETEK Introduction
AGENDA








Introductions
EDETEK Overview
CDISC Compliance
Panther CTMP™
Quality Control
CDISC Data Analytics and Submission Services

2
INTRODUCTION TO EDETEK
Company

CDISC Commitment







 CDISC “Gold Member”
 Member of 6 CDISC Working Groups:
SDS, ADaM, CDASH, ODM, CT, Share
 Participated in CDISC Pilot
 CDISC Registered Solution Provider (RSP)
for SDTM, ADaM, & Define.xml

Services

Quality Work

Full-service CRO established in 2009
Headquarter in Princeton, NJ
Branch office in Beijing
ISO 9001-2008 Certified
Over 50 member team with more than 30
dedicated to CDISC Services
 Partner with multiple clinics in US and 600+
sites in China









 Full data management services to 20
pharmaceutical companies
 Prepared hundreds of study packages
 Completed 4 NDA submission
(including ISS/ISE packages) in 2013
 Customers including largest
pharmaceutical companies
 World-wide data standardization
partner of HCL

Study Design – Protocol Development
Monitoring
Clinical Data/Study Management
Stats and Programming
CDISC Conversion/e-Submission
Medical Writing
Technology & Platform Provider

3
THERAPEUTIC AREA EXPERIENCE
CDISC Involvement

 Oncology

As an example

 Other therapeutic areas











Anti-inflammatory/Pain
Anti-infective
Neurology/CNS
Cardiovascular
Gastroenterology
Ophthalmology
Allergy
Vaccine
PK/PD
Diabetes and metabolic
disease
 Dermatology

 CDISC SDS Oncology SubTeam Member
 CDISC Oncology Terminology
Sub-tem Member

Oncology Library
 Standard Libraries for Solid
and Liquid Tumor
 Endpoints: OS, PFS, ORR, DFS,
TTF, TTP, PRO, QOL
 CTC AE Library

Oncology Module
 Dedicated Oncology Mapping
Module

Submission Experience
 Prepared multiple NDA
Submission Packages
 SDTM, ADaM, TLF, CSR

4
PANTHER CTMP™ – COMPLETE PLATFORM

5
PANTHER CTMPTM GOALS
Standardized & streamlined process
Automated programming
Elimination of redundancy

Performance

Reduced error
Reduced manual efforts
Reduced time /
resource requirements

Cost

Quality

Control
Standard and Metadata driven
Open architecture for integration and access
Elimination of black boxes and bottle necks

Make No Compromise!
6

Built-in QC/QA framework
Single version of truth
Reduction of human errors
Enhanced communication
PANTHER CDMSTM

External System

Unified Access Portal

Web Services

CRF Design

Study Administration

Data Repository

Forms & Items

Study
Management

Data Capture

Presentation
Layout

Site
Management

External Data
Integration

Standardization
(SDTM)

Edit Checks

Investigator
Management

Query
Management

Coding

Standardization
Rules

Patient
Management

Document
Management

Panther CDMSTM

Study Protocol
CDASH
Sponsor
Standards
Edit Check
Library

Data Standardization

Reporting
Monitoring

Administration

7

Coding
COMPREHENSIVE QUALITY CONTROL FRAMEWORK

CRF
Design

Study
Raw Data

SDTM
Data

ADaM &
Results

eCTD

CRF Design
Validation

Study Raw
Data Validation

SDTM Data
Validation

Analysis Data &
Results
Validation

Submission
Package
Validation

Quality Control
Framework

• Quality Check
• Quality Assurance
• Monitoring &
Tracking
• Exception
Resolution
• Reporting

Quality Control
Framework

Repository

8

Web Portal
PANTHER CLINICAL DATA WAREHOUSE

•
•
•
•
•

Explore changes in treatment effect over time
Integrate Summaries of Safety and Efficacy
Integrate existing information
Provide data for rational decision making
Prospective planning in drug development

9
CONTACT INFORMATION

Primary Contact:
President: Jian Chen (jian.chen@edetek.com)

EDETEK, Inc.
1 Independence Way, Suite 405
Princeton, NJ 08540
Phone: 609-720-0888/9
Fax:
609-720-0880
E-mail: info@edetek.com

10

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CDISC Edetek Panther CTMP introduction

  • 2. AGENDA       Introductions EDETEK Overview CDISC Compliance Panther CTMP™ Quality Control CDISC Data Analytics and Submission Services 2
  • 3. INTRODUCTION TO EDETEK Company CDISC Commitment       CDISC “Gold Member”  Member of 6 CDISC Working Groups: SDS, ADaM, CDASH, ODM, CT, Share  Participated in CDISC Pilot  CDISC Registered Solution Provider (RSP) for SDTM, ADaM, & Define.xml Services Quality Work Full-service CRO established in 2009 Headquarter in Princeton, NJ Branch office in Beijing ISO 9001-2008 Certified Over 50 member team with more than 30 dedicated to CDISC Services  Partner with multiple clinics in US and 600+ sites in China         Full data management services to 20 pharmaceutical companies  Prepared hundreds of study packages  Completed 4 NDA submission (including ISS/ISE packages) in 2013  Customers including largest pharmaceutical companies  World-wide data standardization partner of HCL Study Design – Protocol Development Monitoring Clinical Data/Study Management Stats and Programming CDISC Conversion/e-Submission Medical Writing Technology & Platform Provider 3
  • 4. THERAPEUTIC AREA EXPERIENCE CDISC Involvement  Oncology As an example  Other therapeutic areas           Anti-inflammatory/Pain Anti-infective Neurology/CNS Cardiovascular Gastroenterology Ophthalmology Allergy Vaccine PK/PD Diabetes and metabolic disease  Dermatology  CDISC SDS Oncology SubTeam Member  CDISC Oncology Terminology Sub-tem Member Oncology Library  Standard Libraries for Solid and Liquid Tumor  Endpoints: OS, PFS, ORR, DFS, TTF, TTP, PRO, QOL  CTC AE Library Oncology Module  Dedicated Oncology Mapping Module Submission Experience  Prepared multiple NDA Submission Packages  SDTM, ADaM, TLF, CSR 4
  • 5. PANTHER CTMP™ – COMPLETE PLATFORM 5
  • 6. PANTHER CTMPTM GOALS Standardized & streamlined process Automated programming Elimination of redundancy Performance Reduced error Reduced manual efforts Reduced time / resource requirements Cost Quality Control Standard and Metadata driven Open architecture for integration and access Elimination of black boxes and bottle necks Make No Compromise! 6 Built-in QC/QA framework Single version of truth Reduction of human errors Enhanced communication
  • 7. PANTHER CDMSTM External System Unified Access Portal Web Services CRF Design Study Administration Data Repository Forms & Items Study Management Data Capture Presentation Layout Site Management External Data Integration Standardization (SDTM) Edit Checks Investigator Management Query Management Coding Standardization Rules Patient Management Document Management Panther CDMSTM Study Protocol CDASH Sponsor Standards Edit Check Library Data Standardization Reporting Monitoring Administration 7 Coding
  • 8. COMPREHENSIVE QUALITY CONTROL FRAMEWORK CRF Design Study Raw Data SDTM Data ADaM & Results eCTD CRF Design Validation Study Raw Data Validation SDTM Data Validation Analysis Data & Results Validation Submission Package Validation Quality Control Framework • Quality Check • Quality Assurance • Monitoring & Tracking • Exception Resolution • Reporting Quality Control Framework Repository 8 Web Portal
  • 9. PANTHER CLINICAL DATA WAREHOUSE • • • • • Explore changes in treatment effect over time Integrate Summaries of Safety and Efficacy Integrate existing information Provide data for rational decision making Prospective planning in drug development 9
  • 10. CONTACT INFORMATION Primary Contact: President: Jian Chen (jian.chen@edetek.com) EDETEK, Inc. 1 Independence Way, Suite 405 Princeton, NJ 08540 Phone: 609-720-0888/9 Fax: 609-720-0880 E-mail: info@edetek.com 10

Notas do Editor

  1. Removed people/clients. Combined with page 5.
  2. Re-ordered.