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8th International Conference and Exhibition on Pharma Audit, GMP, GCP & Quality Control
June 08-09, 2018 Philadelphia, Pennsylvania, USA
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GMP and Pharma Audit 2018 Report

GMP & Pharma Audit 2018

8th International Conference and Exhibition on Pharma Audit, GMP, GCP & Quality Control which was held during June 08-09, 2018 at Doubletree by Hilton Hotel Philadelphia Airport, Philadelphia, USA. The conference was marked with the attendance of Editorial Board Members of supported OMICS Group Journals, Regulatory professionals, scientists, academicians representing more than 25 countries, who made this conference fruitful and productive.

This conference was based on the theme “Meeting standards of drug regulations & achieving GxP compliance” which included the following scientific tracks:  

Good Manufacturing Practices: The Gap within

Current Regulations and Quality Standards

Current GMP Guidelines (cGMP) & GxP in Pharmaceuticals

The Role of c in cGMP

Good Clinical Practices & Good Laboratory Practices

Quality Control

Quality Assurance

Validation

Contract & Sterile/Aseptic Manufacturing

Storage, Distribution, Transportation

Formulation Development

GMP in Food Industry

GMP in Microbiology and Biotechnology

Softwares in GMP and GCP

Analytical method Quality Auditing

 Excipient Qualification and Supply Chain Controls

Quality Assurance Audits in Pharma Industries

 Quality Management System in Testing Laboratories

 Importance of Audit in Pharmaceutical Industry

 Auditing Deviations, Product Complaints, and CAPA Systems

Goals and Strategies to Meet Audit Requirements

Pharmaceutical Auditing for OTC Drugs

Clinical and Bioanalytical laboratory Audits

Clinical Audit in Pharmaceutical Development

Quality Assurance, Quality Control and Audit

 

GMP & Pharma Audit 2018 was moderated by Joel Finkle, (Acuta LLC, USA) & Raymond C Jagessar (University of Guyana, Guyana)

We are thankful to our below Honourable guests for their generous support and suggestions.

  • Rashid Mahmood- Surge Laboratories, Pakistan
  • R. Manavalan– RVS College of Pharmaceutical Sciences, India

The conference proceedings were carried out through various Scientific-sessions and plenary lectures of which the following topics were highlighted as Keynote-presentations:

  • A blueprint for outsourcing audits of approved GxP validations: Michael D Spangler- Spangler Consulting LLC, USA
  • Quality management and quality audit according to GxP/GMP requirements- Eleonora Babayants, Galaxy Consulting, USA
  • Pharma regulatory affairs as well as importance of ISO 9001:2015, ISO
  • 14001:2004, ISO 18001:2007 standards and related audits for quality pharma products- Manavalan R, RVS College of Pharmaceutical Sciences, India
  • Good manufacturing practices for sterile pharmaceutical products- Rashid Mahmood, SURGE Laboratories Private Limited, Pakistan
  • Various sessions were chaired and co-chaired by: Joel Finkle – Acuta LLC, USA.

Conference Series LLC Ltd has taken the privilege of felicitating GMP & Pharma Audit 2018 Organizing Committee, Editorial Board Members and Keynote Speakers who supported for the success of this event.

The esteemed guests, Keynote speakers, well-known researchers and delegates shared their innovative research and vast experience through their fabulous presentations at the podium of grand GMP & Pharma Audit 2018. We are glad to inform that all accepted abstracts for the conference have been published in OMICS Group Journal of Developing Drugs: Open Access as a special issue.

 

 



Expert Presentations
Michael D Spangler

Spangler Consulting LLC

USA
Manavalan R

RVS College of Pharmaceutical Sciences

India
Rashid Mahmood

SURGE Laboratories Private Limited

Pakistan
Aysu Yurdasiper Erdem

Ege University

Turkey
Jacob Adegboyega Kolawole

University of Jos

Nigeria
James R Bruno

Chemical and Pharmaceutical Solutions, Inc.,

USA
Bernice Brempong

Makhealth Pharmaceuticals Ltd.

GHANA
Conference Secretariat: GMP and Pharma Audit 2018, Conference Series Conferences
47 Churchfield Road, London, W3 6AY, UK,
Tel: +44-800-014-8923 , Fax: +44-203-004-1517
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Operated by: Editors - Journal of Developing Drugs, Pharmaceutica Analytica Acta and Pharmaceutical Regulatory Affairs: Open access
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