Journal of Developing Drugs
Open Access

3^rd International Summit on GMP, GCP & Quality Control

September 25-26, 2014 Valencia Convention Centre, Spain

Keynote

• Current directions for process validation according FDA and EMA

  Victor Sanchez

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• Lowering facility operational cost by energy efficient HVAC system operation

  Sundar Chellamani

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• Practical experience: Integration of different GMP and ISO in the same facilities

  Maria Pellin Amoros

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• Medical devices - Regulatory intelligence - What is it?

  Rama K Pidaparti

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• Defining and managing a corporate quality culture

  David L Chesney

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• Quality of biosimilars produced in developing countries

  Wael Ebied

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• cGMP compliance design of sterile/aseptic manufacturing facilities is a mandatory to meet qualification and validation requirements

  Aziz Chraibi

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