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Nov 2009
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Sun, Nov 8, 2009


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Mon, Nov 9, 2009
How to Implement Risk Management Principles and Activities Within a Quality Management System - Course / Training / Workshop (Dublin, Ireland)

Mon, Nov 9, 2009
Cleanroom Microbiology for the Non-Microbiologist - Course / Training / Workshop (Malvern, PA)

Mon, Nov 9, 2009
Writing Effective Standard Operating Procedures and Other Process Documents - Course / Training / Workshop (Costa Mesa, CA)

Mon, Nov 9, 2009
Generic Drug Approvals: Preparing an ANDA for First-Cycle Approval - Course / Training / Workshop (Malvern, PA)

Mon, Nov 9, 2009
9:00am
7th Annual Vaccines: All Things Considered - Conference (Washington D.C)

Tue, Nov 10, 2009
How to Implement Risk Management Principles and Activities Within a Quality Management System - Course / Training / Workshop (Dublin, Ireland)

Tue, Nov 10, 2009
Cleanroom Microbiology for the Non-Microbiologist - Course / Training / Workshop (Malvern, PA)

Tue, Nov 10, 2009
Writing Effective Standard Operating Procedures and Other Process Documents - Course / Training / Workshop (Costa Mesa, CA)

Tue, Nov 10, 2009
Generic Drug Approvals: Preparing an ANDA for First-Cycle Approval - Course / Training / Workshop (Malvern, PA)

Tue, Nov 10, 2009
Principles of Organic Chemistry - Course / Training / Workshop (Malvern, PA)

Wed, Nov 11, 2009
3rd Annual Stability Testing Conference - Conference (BSG House, London, UK)
Well planned, executed and managed stability studies are critical for understanding data generated during clinical trials. Stability testing is an expensive part of product development, but conducted efficiently, it can save money in latter parts of the lifecycle. Visiongain's 3rd Annual Stability Testing conference will examine developments in technology for stability assessment. As part of this 2-day event, leading authorities will assess the application and limitations of various analytical and statistical methods, as well as study design. Participants will be provided with a reliable evaluation of the principles and techniques associated with the stability testing of biologics and new pharmaceutical products.
Wed, Nov 11, 2009
Pre-Conference Seminar QbD IN INHALATION PRODUCT DEVELOPMENT - Course / Training / Workshop (The Cavendish Hotel, London)
Full Details will follow shortly. Please contact andrea.james@management-forum.co.uk for further information or a brochure.
Wed, Nov 11, 2009
Generic Drug Approvals: Preparing an ANDA for First-Cycle Approval - Course / Training / Workshop (Malvern, PA)

Wed, Nov 11, 2009
Principles of Organic Chemistry - Course / Training / Workshop (Malvern, PA)

Wed, Nov 11, 2009
Sterilization Procedures: Technology, Equipment and Validation - Course / Training / Workshop (Malvern, PA)

Wed, Nov 11, 2009
Reporting Failure Investigations and Process Deviations - Course / Training / Workshop (Dublin, Ireland)

Wed, Nov 11, 2009
PHARMACEUTICAL REGULATORY AFFAIRS IN CHINA - Course / Training / Workshop (The Rembrandt Hotel, London)
This seminar will provide an up-to-date coverage of all aspects playing an important role in gaining and maintaining a successful marketing authorisation for R&D based pharmaceutical products in PR China. In this carefully balanced programme, speakers will cover the underlying official regulatory sources and share the interpretation and practical aspects of putting these into practice in a day-to-day scenario. This seminar will also include an overview of the requirements for local manufacturing as well as of the patent situation and the current legal framework for pharmaceutical patents in PR China. An interactive session has been incorporated into the programme where participants will be invited to put learning into practice through the resolution of a case study. It is anticipated that this seminar will be useful both as an introductory course and as a refresher course to people who need to have an up-to-date and wide knowledge of the subject area.
Thu, Nov 12, 2009
3rd Annual Stability Testing Conference - Conference (BSG House, London, UK)
Well planned, executed and managed stability studies are critical for understanding data generated during clinical trials. Stability testing is an expensive part of product development, but conducted efficiently, it can save money in latter parts of the lifecycle. Visiongain's 3rd Annual Stability Testing conference will examine developments in technology for stability assessment. As part of this 2-day event, leading authorities will assess the application and limitations of various analytical and statistical methods, as well as study design. Participants will be provided with a reliable evaluation of the principles and techniques associated with the stability testing of biologics and new pharmaceutical products.
Thu, Nov 12, 2009
INHALED DRUG DELIVERY (IDD) - Course / Training / Workshop (Le Meridien Piccadilly, London)

Thu, Nov 12, 2009
Sterilization Procedures: Technology, Equipment and Validation - Course / Training / Workshop (Malvern, PA)

Thu, Nov 12, 2009
Reporting Failure Investigations and Process Deviations - Course / Training / Workshop (Dublin, Ireland)

Thu, Nov 12, 2009
Preparing the CMC Section for NDAs/INDs/CTDs - Course / Training / Workshop (King of Prussia, PA)

Thu, Nov 12, 2009
Writing in the Regulated Environment When English Is Your Second Language - Course / Training / Workshop (Costa Mesa, CA)

Thu, Nov 12, 2009
Principles of Analytical Chemistry - Course / Training / Workshop (Malvern, PA)

Thu, Nov 12, 2009
PHARMACEUTICAL REGULATORY AFFAIRS IN CHINA - Course / Training / Workshop (The Rembrandt Hotel, London)
This seminar will provide an up-to-date coverage of all aspects playing an important role in gaining and maintaining a successful marketing authorisation for R&D based pharmaceutical products in PR China. In this carefully balanced programme, speakers will cover the underlying official regulatory sources and share the interpretation and practical aspects of putting these into practice in a day-to-day scenario. This seminar will also include an overview of the requirements for local manufacturing as well as of the patent situation and the current legal framework for pharmaceutical patents in PR China. An interactive session has been incorporated into the programme where participants will be invited to put learning into practice through the resolution of a case study. It is anticipated that this seminar will be useful both as an introductory course and as a refresher course to people who need to have an up-to-date and wide knowledge of the subject area.
Fri, Nov 13, 2009
INHALED DRUG DELIVERY (IDD) - Course / Training / Workshop (Le Meridien Piccadilly, London)

Fri, Nov 13, 2009
Reporting Failure Investigations and Process Deviations - Course / Training / Workshop (Dublin, Ireland)

Fri, Nov 13, 2009
Preparing the CMC Section for NDAs/INDs/CTDs - Course / Training / Workshop (King of Prussia, PA)

Fri, Nov 13, 2009
Writing in the Regulated Environment When English Is Your Second Language - Course / Training / Workshop (Costa Mesa, CA)

Fri, Nov 13, 2009
Principles of Analytical Chemistry - Course / Training / Workshop (Malvern, PA)

Fri, Nov 13, 2009
9:00am
Surviving as a Woman in Science - Conference (BioPark Hertfordshire, Welwyn Garden City)
With talks such as "Do women make a difference to biology, and does biology make a difference to women?" (Professor Sian Harding, Imperial College, London) and "PhD and Business" (Dr Mitra Hedman, SolXO Ltd, UK) this event will be extremely interesting for women working in science.
Mon, Nov 16, 2009
3rd Annual Contract Manufacturing in Pharma and Biotech Conference - Conference (BSG House, London, UK)
The recent surge in contract manufacturing landscape is influencing huge challenges and opportunities in the global pharmaceutical market. The highly competitive nature of the industry has been driving pharma and biotech companies to set up off-shoring alliances with emerging markets to minimise costs and maximise profits.
Mon, Nov 16, 2009
Chromatin: Structure & Function Conference 2009 - Conference (Hilton Papagayo Resort, Costa Rica)

Mon, Nov 16, 2009
SCIENTIFIC ADVICE - Optimising Regulatory Input Into Drug Development - Seminar (The Rembrandt Hotel, London)
Obtaining the right scientific advice at the right time can make or break a drug development programme, and companies are willing to invest considerable time & resources in managing scientific advice procedures. It is now seen as being essential rather than optional to obtain input from the regulatory authorities at key stages of development. This seminar will examine the routes available for obtaining scientific advice in Europe, provide insight as to how to manage these procedures effectively and discuss how to incorporate scientific advice into development programmes. Additionally an overview of the new NICE Scientific Advice Consultancy Service will be provided.
Mon, Nov 16, 2009
GENERIC MEDICINES/IP LEGAL & REGULATORY ISSUES - to be held in India - Course / Training / Workshop (Taj Lands End, Mumbai, India)
The aim of this seminar is to shed some light on the legal background to the European generic industry and to provide an understanding of how it affects all parts of the business.
Mon, Nov 16, 2009
Good Clinical Practices (GCPs) - Course / Training / Workshop (Malvern, PA)

Mon, Nov 16, 2009
SCIENTIFIC ADVICE - Optimising Regulatory Input Into Drug Development - Course / Training / Workshop (Hotel to be advised, London)
This seminar will examine the routes available for obtaining scientific advice in Europe (including covering the recent changes to the CPMP and MHRA procedures), as well as in the US and Japan, and will explore the means of securing the best possible input and integrating advice from several different sources into a single global development programme.
Mon, Nov 16, 2009
9:00am
Generic Medicine: IP / Legal and Regulatory Issues - Seminar (TAJ Hotels)
To be held in 3 Indian cities: Mumbai, Delhi and Hyderabad. The aim of this seminar is to shed some light on the legal background to the European generic industry and to provide an understanding of how it affects all parts of the business. Topics to be covered include:  Understand the European Generic marketplace  Patents and how they affect generics  Data Exclusivity  DCP and European Regulatory System  Key aspects of European legislation
Tue, Nov 17, 2009
3rd Annual Contract Manufacturing in Pharma and Biotech Conference - Conference (BSG House, London, UK)
The recent surge in contract manufacturing landscape is influencing huge challenges and opportunities in the global pharmaceutical market. The highly competitive nature of the industry has been driving pharma and biotech companies to set up off-shoring alliances with emerging markets to minimise costs and maximise profits.
Tue, Nov 17, 2009
Chromatin: Structure & Function Conference 2009 - Conference (Hilton Papagayo Resort, Costa Rica)

Tue, Nov 17, 2009
Good Clinical Practices (GCPs) - Course / Training / Workshop (Malvern, PA)

Tue, Nov 17, 2009
Pharmaceutical Water Systems - Contem