1 / 13

India Seminar 2013 on “Good Laboratory Practice Regulations

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

globalcompliancepane
Télécharger la présentation

India Seminar 2013 on “Good Laboratory Practice Regulations

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  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 All rights are reserved © GlobalCompliancePanel.

  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. All rights are reserved © GlobalCompliancePanel.

  3. OVERVIEW 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. 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.  All rights are reserved © GlobalCompliancePanel.

  4. Course Outline Day 1 - 21st March 2013 Day 2 – 22nd March 2013 All rights are reserved © GlobalCompliancePanel.

  5. Who Will Benefit All rights are reserved © GlobalCompliancePanel.

  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. All rights are reserved © GlobalCompliancePanel.

  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 All rights are reserved © GlobalCompliancePanel.

  10. Register Online Reach Us At: www.globalcompliancepanel.com All rights are reserved © GlobalCompliancePanel.

  11. Clients GlobalCompliancePanel Partial Client List All rights are reserved © GlobalCompliancePanel.

  12. Where we are Planning to do our Conferences UK Bengaluru, India HQ Wilmington, DE, USA CA, USA Malaysia Dubai Singapore Chennai, India All rights are reserved © GlobalCompliancePanel.

  13. Contact Information: Event Coordinator Toll free: 1800 425 9409 Fax: +91 80-2642-1483 Email: customersupport@globalcompliancepanel.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 All rights are reserved © GlobalCompliancePanel.

More Related