'Pharmaceutical products' presentation slideshows

Trends in Europe: Coping with National Differences in Regulation of Marketing Practices and Relationships with Health P

Trends in Europe: Coping with National Differences in Regulation of Marketing Practices and Relationships with Health Professionals. 6 June 2007, Brussels International Pharmaceutical Regulatory and Compliance Congress and Best Practice Forum. Linda R. Horton, Partner

990 views • 72 slides

2k views • 59 slides

Care required to draft pharma patents and prosecution of pharma patents

Care required to draft pharma patents and prosecution of pharma patents. Ahmedabad, November 26, 2006 Kiyoshi Kuzuwa Patent Attorney KUZUWA & PARTNERS Tokyo, Japan. Care required to draft pharma patents and prosecution of pharma patents. I. Patentability on pharmaceutical/medical

1.39k views • 51 slides

Bioequivalence studies: Regulatory Requirements on Conduct & Documentation of BE. Guidance & Experience.

1.44k views • 47 slides

STABILITY STUDIES

STABILITY STUDIES. GABRIEL K. KADDU Head, Drug assessment and Registration National Drug Authority Uganda.

7.05k views • 38 slides

Supply Solutions for Children

Supply Solutions for Children. Agenda. Procurement statistics Major commodity areas Drug Procurement Sourcing and Special Procurement Supplier Registration and Evaluation Case Study. Procurement. Total Procurement 2000: $502 million. Offshore: $288 million

466 views • 32 slides

Pan American Network for Drug Regulatory Harmonization Steering Committee Meeting Mexico City May 7-8, 2003

Pan American Network for Drug Regulatory Harmonization Steering Committee Meeting Mexico City May 7-8, 2003. Bioequivalence Working Group. Justina A. Molzon, M.S. Pharm., J.D. Associate Director for International Affairs Center for Drug Evaluation and Research/USFDA.

639 views • 31 slides

WHO inspections of Contract Research Organizations

WHO inspections of Contract Research Organizations. The prequalification project.

620 views • 31 slides

Windsor Sathyam Separation Systems

761 views • 31 slides

Purification strategies

Purification strategies. By : Miss Thida Chanyachukul AIDs Production group. Outline. General concepts in Purification strategies Principle of purification operations Special considerations in our biopharmaceutical products Ritonavir (Protease inhibitor) Vaccine IL-2 Conclusions

990 views • 29 slides

Industrial & Innovation Policy

592 views • 28 slides

445 views • 28 slides

Training Workshop on Dissolution, Pharmaceutical Product Interchangeability and Biopharmaceutical Classification System.

Multisource (generic) products and Interchangeability . Training Workshop on Dissolution, Pharmaceutical Product Interchangeability and Biopharmaceutical Classification System. Hotel Bratislava 1 Malyshko Street Kyiv, Ukraine Date: 25 to 27 June 2007.

845 views • 27 slides

Supplementary T raining Workshop on Good Manufacturing Practices (GMP)

631 views • 26 slides

Regulatory principles reflected in practice of WHO PQP

Regulatory principles reflected in practice of WHO PQP. Milan Smid, M.D., Ph.D. Prequalification Programme: Priority Essential Medicines. Principle approaches to regulatory assessment of medicines Innovative & generic medicines Structure of the dossier of medicinal product

542 views • 25 slides

Test Data Protection Overview

BEIJING BRUSSELS CHICAGO DALLAS FRANKFURT GENEVA HONG KONG LONDON LOS ANGELES NEW YORK PALO ALTO SAN FRANCISCO SHANGHAI SINGAPORE SYDNEY TOKYO WASHINGTON, D.C. Test Data Protection Overview. Jeffrey P. Kushan, Washington, D.C.

449 views • 23 slides

Risk-Based Sourcing for Bovine Materials in FDA-regulated Medical Products: Introduction and General Considerations

Risk-Based Sourcing for Bovine Materials in FDA-regulated Medical Products: Introduction and General Considerations. FDA TSE Advisory Committee Meeting Holiday Inn Silver Spring MD 12 February 2004 David M. Asher, MD Laboratory of Bacterial, Parasitic and Unconventional Agents

535 views • 20 slides

Quality Management

Basic Principles of GMP. Quality Management. Section 1 and 2. Quality Management. Objectives To understand key issues in quality assurance/good manufacturing practices/quality control. To understand specific requirements on quality management and quality assurance including:

836 views • 19 slides

Regulatory Requirements for BE

1.26k views • 18 slides

Pharmaceutical Industry Executive Lists

Providing Highly Targeted, Precise & 100% Permission Based Pharmaceutical Industry Executives Lists

471 views • 8 slides