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HUM-MOLGEN
-> Events
-> Meetings and Conferences |
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June 12, 2011 |
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Hotel The Park , Hyderabad India
Sep 15 2011 7:00AM - Sep 17 2011 3:00PM
CONFERENCE OBJECTIVE
This conference is organized in cooperation with World Health Organization
(WHO), The European Directorate for the Quality of Medicine & Health Care
(EDQM) and Drug Information Association (DIA). The major focus of this
conference will be on the current regulatory requirements for the quality of
API, Compliance with GMP Standards from Global Regulatory Authorities
Perspective. The conference will also focus on the current issues of Pharmacopoeial
Monographs, as well as API Certifi cation and WHO Prequalification requirements. FEATURED TOPICS
• Regulatory requirements with relevance for quality of API Compliance of API manufacturers with current GMP Standards
• Current issues and challenges in the development of Pharmacopoeial Monograph
• API Certification and WHO Prequalification Program
Learning Objectives:
At the conclusion of this meeting, participants should be able to:
• Describe the regulatory issues of API manufacturing and compliance
• Explain the current compliance issues of API
• Discuss the requirements of the API under the WHO Prequalification Programme
• Outline the procedures for Certification of Suitability (CEP)
Event Code:
11658
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Organized by:
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DIA India |
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Invited Speakers:
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See website for speaker information
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Deadline for Abstracts:
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Call contact
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Registration:
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REGISTRATION: Pallavi Gokhale, Executive Program Development & Operations, DIA (India)
Private Limited; Cell: +91-9004682564 ; Fax: +91-22-2859-4762; Email: Pallavi.Gokhale@
diaindia.org or Shailendra Singh, Marketing and Promotion Executive; Email: shailendra.
singh@diaindia.org, +91-22-9223267327
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E-mail:
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pallavi.gokhale@diaindia.org
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WWW: Kai Garlipp,
Frank S.
Zollmann.
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