(18 results)(Back to Archives)

*Pharma Pricing & Market Access Outlook Europe 2011
London, United Kingdom
22 Mar 2011 - 25 Mar 2011
It is a two day strategic conference addresssing the critical policy issues in developing the optimum pricing strategy for pharmaceutical products..

*Clinical Outsourcing World Europe 2011
London, United Kingdom
8 Feb 2011 - 11 Feb 2011
The congress for outsourcing executives and decision makers.

*Design Validation Protocol and Acceptance Criteria for Chromatographic Methods
Palo Alto, United States
9 Dec 2010 - 9 Dec 2010
This Design validation 4 hour session will discuss how to write validation protocol and determine acceptance criteria. It will also explain the systematic approach to validate analytical procedures..

*Health Technology Assessment World Europe 2010
London, United Kingdom
7 Dec 2010 - 10 Dec 2010
Find out the latest developments in HTA policy in Europe, USA & Asia..

*Why and How - Verification of Compendial Methods - USP
Palo Alto, United States
30 Nov 2010 - 30 Nov 2010
This verification of Compendial methods webinar training will discuss the requirements of USP , what are FDA expectations related to method verification..

*Disinfectant Validation and Cleanroom Cleaning for all FDA and EMEA regulated companies
Palo Alto, United States
9 Nov 2010 - 9 Nov 2010
This Disinfection and Cleanroom Cleaning training will teach you how to choose the best disinfectants, know the different performance parameters of disinfectants, methods to qualify disinfectants, writing and executing cleaning procedures..

*Monitoring Impurities in Pharmaceutical Products to meet ICH Q3 A/B Requirements
Palo Alto, United States
27 Oct 2010 - 27 Oct 2010
This pharma training will discuss how to monitor impurities in pharmaceutical products as per ICH Q3 A/B requirements and learn how to measure the thresholds to report for regulatory submission..

*Drug Safety Assessment and Risk Minimization in the Development Period
Palo Alto, United States
26 Oct 2010 - 26 Oct 2010
This drug safety training will discuss the various factors to be considered and the principles of risk assessment to be followed during drug development to minimize risk..

*Solutions for Addressing Fungal and Bacterial Spore Outbreaks in Pharmaceutical Operations
Palo Alto, United States
21 Oct 2010 - 21 Oct 2010
This contamination control webinar will discuss how personnel practices, transferring items into cleanrooms, facility design, construction, and sporicidal chemistries are critical and how it can be addressed in developing a successful contamination contro.

*Data Monitoring Committees (DMCs) effect on subject safety in clinical research and how to set it up to be effective
Palo Alto, United States
12 Oct 2010 - 12 Oct 2010
This Data Monitoring Committees (DMC) webinar will guide you through the essential and the purpose of the Data and Safety monitoring plan..

*GMPs in Biopharmaceutical Development Laboratories
Palo Alto, United States
1 Oct 2010 - 1 Oct 2010
This GMP webinar training on Biopharmaceutical lab provides the attendee with an overview of the GMPs as they pertain to early phase development labs. This course satisfies the annual mandatory training required for personnel employed in GMP laboratories..

*The Hero of Manufacturing Contamination Control -- The Microbiology Lab
Palo Alto, United States
22 Sep 2010 - 22 Sep 2010
This webinar on Contamination Control will discuss, how the micro lab can be more effectively utilized to prevent or head off microbial contamination issues as well as effectively resolve problems like recurring micro failures.

*Stability Program to support Shipping and Distribution of Drug Products
Palo Alto, United States
22 Sep 2010 - 22 Sep 2010
Learn key factors affecting shipping and distribution of product and the stability studies that should be done to support shipping and distribution..

*The role of Analytical Program to Support Drug Development Process
Palo Alto, United States
14 Sep 2010 - 14 Sep 2010
This drug development process training Webinar will give an overview of drug development process, the regulatory requirements and the analytical technology used for pharmaceutical analysis supporting R & D..

*Engineering and Laboratory Mythology with Water System
Palo Alto, United States
8 Sep 2010 - 8 Sep 2010
This water systems webinar training will discuss the myths surrounding microbial monitoring and control approaches and alert you to the pitfalls of believing these myths which could cause over-confidence in a systemís design.

*Process Validation for Drugs and Biologics
Palo Alto, United States
25 Aug 2010 - 25 Aug 2010
In this Process Validation training learn how to validate a manufacturing process and do it in a reasonable time..

*Streamline Documentation System in Pharmaceutical Laboratory
Palo Alto, United States
11 Aug 2010 - 11 Aug 2010
This laboratory documentation training Webinar will discuss the GMP requirements on laboratory records and how to streamline documentation system..

*Key Factors to Write an Effective Standard Operating Procedure (SOP)
Palo Alto, United States
22 Jul 2010 - 22 Jul 2010
In this Effective Standard Operating Procedure (SOP) training learn how to develop a comprehensive, consistent SOP. The critical elements of a SOP which is easier to understand follow and review by operating personnel..

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