India Seminar 2013 on “Good Laboratory Practice Regulations - Introduction and Strategies for Implementation” at Mumbai - PowerPoint PPT Presentation

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Title: India Seminar 2013 on “Good Laboratory Practice Regulations - Introduction and Strategies for Implementation” at Mumbai


1
INDIA SEMINAR AT MUMBAI
2-day In-person Seminar on Good Laboratory
Practice Regulations - Introduction and
Strategies for Implementation at Mumbai
DATE
AT
The Lalit Hotel Sahar Airport, Andheri
East.from 9 am to 6 pm EST at The Lalit Mumbai 
March 21 and 22, 2013
2
Kindly find below the Benefits of attending the
GLP Seminar
  • Two days of seminar by the renowned speaker, Dr.
    Steven S. Kuwahara
  • Complete training material of the workshop
  • Two networking tea breaks, where you can interact
    with your peers in the Industry
  • Post seminar e-mail assistance directly from the
    speaker
  • Participation Certificate
  • Q A sessions after each lecture, which gives
    you an opportunity to explore and evaluate the
    challenges and various issues not only with the
    speaker but also with 25 to 30 different
    companies delegates
  • Buffet lunch at the 5-star hotel.

3
Course "Good Laboratory Practice Regulations -
Introduction and Strategies for Implementation"
has been pre-approved by RAPS as eligible for up
to 12 credits towards a participant's RAC
recertification upon full completion.
OVERVIEW
This course will present the regulations and
guidelines that apply to the safety testing of
medical products and also discuss the rules as
they apply to testing laboratories that study
samples derived from test animals or test
subjects in clinical studies. The purpose of the
course will be to instruct laboratory personnel
in the material that they must know or prepare to
pass an FDA inspection. The course will also
discuss the types of studies that come under the
GLP regulations. 
4
Course Outline
Day 1 - 21st March 2013
Day 2 22nd March 2013
5
Who Will Benefit
6
Why Should you Attend
Any pharmaceutical worker who performs,
supervises or reviews non-clinical studies
related to product safety should attend this
course. This includes workers who perform studies
on samples derived from animals or clinical
subjects and anyone performing, supervising or
reviewing non-clinical safety studies on any type
of product that is regulated by the U.S. Food and
Drug Administration. Regulatory Affairs workers
who prepare submissions for regulatory agencies
also need to be aware of these regulations and
their requirements, as they are needed for
regulatory submissions.
7
What you get
  • 1.Learning Objectives
  • 2. Participation certificates
  • 3. Interactive sessions with the US expert
  • 4. Post event email assistance to your queries.
  • 5. Special price on future purchase of web based
    trainings.
  • 6. Special price on future consulting or
    expertise services.
  • 7. Special price on future seminars by
    GlobalCompliancePanel.
  • 8. Seminar Kit includes presentation handout,
    ID card, brochure,
  • trainings catalog, notepad and pen.
  • 9. Networking with industry's top notch
    professionals

www.globalcompliancepanel.com
All rights are reserved GlobalCompliancePanel.
8
ABOUT SPEAKER
  • Dr. Steven S. Kuwahara Ph.D. is the
    founder and Principal of GXP Biotechnology LLC, a
    consulting firm that works in the areas covered
    by the GLP and GMP of drugs, biologics, and
    nutraceuticals.
  • Steve has over 30 years of experience in
    supervising quality control laboratories,
    including an animal testing facility, and in
    performing GLP and GMP audits of internal and
    external testing laboratories.
  • Steve has participated in the development of
    drugs and biological through all phases of
    clinical research and final product production.

Dr . Steven S Kuwahara, President of
GlobalCompliancePanel Consulting
All rights are reserved GlobalCompliancePanel.
9
Our Previous Seminar Photos
10
Register Online
Reach Us At
www.globalcompliancepanel.com
All rights are reserved GlobalCompliancePanel.
11
Clients
GlobalCompliancePanel Partial Client List
12
Where we are Planning to do our Conferences
UK
Bengaluru, India HQ
Wilmington, DE, USA
CA, USA
Malaysia
Dubai
Singapore
Chennai, India
13
Contact Information
Event Coordinator Toll free 1800 425 9409 Fax
91 80-2642-1483 Email customersupport_at_globalcomp
liancepanel.com Net Zealous GlobalCompliancePanel
NetZealous Services India Pvt. Ltd. 4th Floor,
'A' Block,Brigade Software Park,Banashankari 2nd
stage, Bangalore-560070, INDIA
www.globalcompliancepanel.in
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