Wednesday, April 07, 2010

Pharmaceutical Events. (Posted: April 2010)| PharmiWeb.com

Pharmaceutical Events - PharmiWeb.com
Upcoming events in the Pharmaceutical Industry.

ISO 14971:2007 and the CE-Mark
From 09 April 2010 to 09 April 2010
This ISO 14971:2007and CE-Mark training will help in understanding the elements of your product risk management file and how to comply with ISO 14971 or ICH Q9.

Venue: Online Event

Requirements of validation and control of EO Sterilization
From 09 April 2010 to 09 April 2010
This EO Sterilization training will help you in understanding how EO sterilization works, the equipment involved, major issues with product sterilization via EO, and the validation requirements. Routi

Venue: Online Event

Cardiovascular Safety in Drug Development: QT, Arrhythmias, Thrombosis, and Bleeding
From 11 April 2010 to 13 April 2010

Venue: Arlington, VA 22204

Collaborations, Deals and Alliances Congress
From 11 April 2010 to 14 April 2010

Venue: .

SBS 16th Annual Conference & Exhibition: Advancing the Science of Drug Discovery
From 11 April 2010 to 15 April 2010
Advancing the Science of Drug Discovery

Venue: Phoenix, AZ, USA

Overview of Drug Development
From 12 April 2010 to 12 April 2010

Venue: Horsham, PA USA

How to Monitor Clinical Trials for GCP Compliance
From 12 April 2010 to 13 April 2010

Venue: King of Prussia, PA, USA

Best Practices for Facilities and Utilities Design, Qualification and Monitoring
From 12 April 2010 to 13 April 2010

Venue: King of Prussia, PA, USA

Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
From 12 April 2010 to 13 April 2010

Venue: Berlin, Germany

An Essential Guide To Pharmacovigilance
From 12 April 2010 to 12 April 2010

Venue: The Rembrandt Hotel, London

Clinical Development of Stem Cell Therapies: Scientific, Regulatory and Ethical Considerations
From 12 April 2010 to 13 April 2010

Venue: North Bethesda, MD 20852

Conference On Pre-Filled Syringes Americas(Conference And Workshop) 
From 12 April 2010 to 14 April 2010
Realising high performance through innovation in injection devices and parental packaging system

Venue: Philadelphia, USA

Conference on Pre-filled Syringes Americas(Workshop Only)  
From 12 April 2010 to 14 April 2010
Pre-filled Syringes Americas Realising high performance through innovation in injection devices and parental packaging system

Venue: Philadelphia, USA

Conference On Pre-Filled Syringes Americas ( Conference Only) 
From 12 April 2010 to 14 April 2010
Pre-filled Syringes Americas Realising high performance through innovation in injection devices and parental packaging system

Venue: Philadelphia, USA

An Essential Guide To Pharmacovigilance
From 12 April 2010 to 12 April 2010

Venue: The Rembrandt Hotel, London

Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
From 12 April 2010 to 13 April 2010

Venue: Dublin, Ireland

Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
From 12 April 2010 to 14 April 2010

Venue: Berlin, Germany

Prescription Drug Labeling Regulation
From 12 April 2010 to 13 April 2010

Venue: Arlington, VA USA

Leadership Essentials
From 13 April 2010 to 14 April 2010

Venue: Beaumont House, Windsor

The 4th Annual Conference in Japan for Asian New Drug Development
From 13 April 2010 to 14 April 2010

Venue: Tokyo 134-0091 Japan

Reducing Ethylene Oxide (EO) Sterilization costs while maintaining regulatory compliance
From 14 April 2010 to 14 April 2010
In this Ethylene Oxide (EO) Sterilization training learn how to evaluate your sterilization process for cost reduction, and will learn how to implement such changes without jeopardizing product safety

Venue: Online Event

NASAL DRUG DELIVERY
From 14 April 2010 to 15 April 2010

Venue: Hotel to be Advised, London

GMP Chapter Effective Quality Assurance Auditing
From 14 April 2010 to 15 April 2010

Venue: Montrel, Canada

Investigating Out-of-Specification (OOS) Results
From 14 April 2010 to 15 April 2010
for Pharmaceutical, Biotechnology, Medical Devices and Allied Industries

Venue: Prague, Czech Republic

Effective Qualification and Monitoring of Processing Equipment and their Control Systems
From 14 April 2010 to 15 April 2010

Venue: King of Prussia, PA, USA

CMC Regulatory Compliance for Biopharmaceuticals and Biologics
From 14 April 2010 to 16 April 2010

Venue: Berlin, Germany

BIOTECHNOLOGY FOR THE NON-BIOTECHNOLOGIST
From 14 April 2010 to 16 April 2010

Venue: Radisson SAS Hotel, Nice, France

Advances in Cell Culture technology
From 15 April 2010 to 15 April 2010

Venue: The BioPark, Hertfordshire , UK

Writing Effective Standard Operating Procedures and Other Process Documents
From 15 April 2010 to 16 April 2010

Venue: Berlin, Germany

Conference on Pricing and Reimbursement for Medical Devices  
From 15 April 2010 to 16 April 2010
Pricing & Reimbursement for Medical Devices Steering towards commercial success through value-based pricing and reimbursement

Venue: BSG Conference Centre

Health Product Liability in the EU
From 15 April 2010 to 15 April 2010
Specialist Life Sciences law firm Bird & Bird present a one day conference with guest speakers on Health Product Liability in the EU

Venue: Hôtel Scribe, 1 rue Scribe, 75009 Paris

Patent and Other Intellectual Property Law for the Life Sciences Industry
From 15 April 2010 to 16 April 2010

Venue: Costa Mesa, CA

FIP Quality International 2009
From 15 April 2010 to 16 April 2010

Venue: Royal Pharmaceutical Society of Great Britain, London

Development of a Clinical Study Report
From 16 April 2010 to 16 April 2010

Venue: Horsham, PA USA

4th Annual FDA/DIA Statistics Forum
From 18 April 2010 to 21 April 2010

Venue: North Bethesda, MD 20852-2785

Essentials of Project Management
From 19 April 2010 to 21 April 2010

Venue: Horsham, PA USA

Effective Quality Assurance Auditing for FDA Regulated Industries
From 19 April 2010 to 20 April 2010

Venue: Costa Mesa, CA

cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
From 19 April 2010 to 21 April 2010

Venue: Dublin, Ireland

Biostatistics for Non - Statisticians
From 19 April 2010 to 21 April 2010

Venue: King of Prussia, PA, USA

QA/QC Strategy for Biopharmaceuticals and Biologics
From 19 April 2010 to 21 April 2010

Venue: Berlin, Germany

Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
From 19 April 2010 to 20 April 2010

Venue: Berlin, Germany

Biology and CMC Strategies in the Nonclinical Development of Pharmaceuticals
From 19 April 2010 to 23 April 2010

Venue: Madison, WI, USA

Advancing Protein Therapeutics
From 20 April 2010 to 22 April 2010
Advancing Protein Therapeutics

Venue: Frankfurt, Germany

Pediatric Clinical Trial Design - Ethics, Management and Regulatory Requirements
From 20 April 2010 to 21 April 2010

Venue: King of Prussia, PA, USA

Understanding International Standards for Medical Devices
From 20 April 2010 to 20 April 2010
This medical device training on International Standards will address various sources of external standards, how they are developed and the differences from region to region.

Venue: Online Event

FDA Clinical Trial Requirements, Regulations, Compliance and GCP
From 20 April 2010 to 20 April 2010
In this FDA clinical trial training get guidance and learn to interpret various clinical trial requirements and regulations. The general scientific principles for the conduct, performance and control

Venue: Online Event

Master Validation Planning and Tougher U.S. FDA & MDD Mod 5
From 20 April 2010 to 20 April 2010
This Master Validation Planning training will evaluate how to do Validation and Verification under the current changes came due to the March 2010 Mod 5 changes to the EU MDD.

Venue: Online Event

GCP violations and Site Mistakes commonly found During a FDA Investigator Site Inspection
From 20 April 2010 to 20 April 2010
This GCP training will guide you through key component identification of a good GCP audit program, Investigator awareness, Protocol adherence, The Informed Consent process, Evaluation of subject selec

Venue: Online Event

Effective Matrix Management
From 20 April 2010 to 20 April 2010

Venue: Beaumont House, Windsor

Introduction to Portfolio Management and Performance Metrics
From 20 April 2010 to 21 April 2010

Venue: Horsham, PA USA

World Drug Safety Congress Americas 2010
From 20 April 2010 to 23 April 2010
2nd annual event

Venue: The Westin Grand, Washington DC

The Pharma Market Access Course
From 20 April 2010 to 21 April 2010
by LLoyd Morgan

Venue: Sheraton Brussels Airport Hotel

4th European Forum for Qualified Person for Pharmacovigilance (QPPV)
From 21 April 2010 to 22 April 2010

Venue: Hilton London Metropole

Process Validation for Medical Devices
From 21 April 2010 to 23 April 2010

Venue: Costa Mesa, CA

The Drug Development Process - From Discovery to Commercialization
From 21 April 2010 to 23 April 2010

Venue: Costa Mesa, CA

Computer Systems Validation in the Pharmaceutical Industry
From 21 April 2010 to 22 April 2010
Stopping the bureaucratic nightmare - Making CSV fit for purpose

Venue: Crowne Plaza Hotel - St James, London, United Kingdom

Developing Successful Partnerships
From 21 April 2010 to 21 April 2010

Venue: Beaumont House, Windsor

4th European Forum for Qualified Person for Pharmacovigilance (QPPV)
From 21 April 2010 to 22 April 2010

Venue: London UK

Asthma & COPD
From 21 April 2010 to 22 April 2010

Venue: London Marriott Hotel Regents Park

GOOD ENGINEERING PRACTICE: (GEP)
From 21 April 2010 to 22 April 2010

Venue: The Rembrandt Hotel, London

What are DHF, DMR and DHR? - The FDA Quality Systems Regulations Records Explained
From 22 April 2010 to 22 April 2010
This Webinar will describe, explain and clarify the differences between DHF, DMR and DHR . It will also detail the requirements and the expected contents of each record.

Venue: Online Event

2nd Annual Drug Development Congress
From 22 April 2010 to 23 April 2010
Registration Closing - over 120 attendees at this year's Drug Development Congress

Venue: Copthorne Tara, Kensington, London

Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
From 22 April 2010 to 23 April 2010

Venue: Dublin, Ireland

Introduction to Statistical Analysis of Laboratory Data
From 22 April 2010 to 23 April 2010

Venue: King of Prussia, PA, USA

2nd Annual Drug Development Congress
From 22 April 2010 to 23 April 2010
Registration Closing - Spaces still available for the 2nd Annual Drug Development COngress, netowkr with over 120 Senior level attendees

Venue: Copthorne Tara, Kensington, London

Process Validation for Drugs and Biologics
From 22 April 2010 to 22 April 2010

Venue: Online Event

Diabetes Clinical Experience Programme
From 22 April 2010 to 23 April 2010
Diabetes Clinical Experience Programme

Venue: Derby

US FDA Inspection Readiness - Preparing For Success
From 22 April 2010 to 23 April 2010

Venue: Harrington Hall Hotel, London

Repairing the Body
From 22 April 2010 to 23 April 2010
Cranfield University's first health conference

Venue: Cranfield, Bedfordshire

High Performance Biopharm Teams
From 22 April 2010 to 23 April 2010

Venue: Horsham, PA USA

Project Information, Communication, and Knowledge Management
From 22 April 2010 to 23 April 2010

Venue: Horsham, PA USA

Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
From 22 April 2010 to 23 April 2010

Venue: Berlin, Germany

Introduction to Effective Medical Writing
From 22 April 2010 to 23 April 2010

Venue: Berlin, Germany

Understanding Acceptance Activities for Medical Devices
From 23 April 2010 to 23 April 2010
This Medical Device Training will help you in understanding clarity about acceptance activities regulatory requirements and how to plan effective and compliant acceptance activities. Discussion on war

Venue: Online Event

The Summary Of Product Characteristics: Construction & Harmonisation
From 23 April 2010 to 23 April 2010

Venue: Harrington Hall Hotel, London

PHARMACOVIGILANCE FOR SUPPORT STAFF
From 23 April 2010 to 23 April 2010

Venue: The Rembrandt Hotel, London

Introduction to Signal Detection and Data Mining in Pharmacovigilance in Europe
From 26 April 2010 to 26 April 2010

Venue: Paris France

Good Management of Medical Devices
From 26 April 2010 to 28 April 2010

Venue: Paris France

An Introduction to Product Information Management (PIM)
From 26 April 2010 to 27 April 2010

Venue: VIenna Austria

CTD Dossier Requirements: Focus on EU Module 1 and Quality Module 3
From 26 April 2010 to 28 April 2010

Venue: Vienna Austria

Standard Pharmaceutical Care Record Stakeholder Day
From 26 April 2010 to 26 April 2010

Venue: The Royal Pharmaceutical Society headquarters, London

Good Management of Medical Devices
From 26 April 2010 to 28 April 2010

Venue: Marriott Rive Gauche

An Introduction to Product Information Management (PIM)
From 26 April 2010 to 27 April 2010

Venue: Hotel Austria Trend Savoyen | Vienna | Austria

CTD Dossier Requirements: Focus on EU Module 1 and Quality Module 3
From 26 April 2010 to 28 April 2010

Venue: Hotel Austria Trend Savoyen | Vienna | Austria

High Throughput Screening
From 26 April 2010 to 27 April 2010
The Route to Intelligent Screening

Venue: Crowne Plaza Hotel – St James, London

Successful eCTD Lifecycle Management
From 26 April 2010 to 28 April 2010

Venue: Canary Wharf - London

Managing The Legal Aspects Of Multi-National Clinical Trials
From 26 April 2010 to 26 April 2010

Venue: The Rembrandt Hotel, London

QUALITY MANAGEMENT SYSTEMS - Part of the Medical Device Training Academy Series
From 26 April 2010 to 26 April 2010

Venue: MWB Business Exchange, Fleet Street, London EC4A

Optimising Clinical Development in Oncology
From 26 April 2010 to 28 April 2010
With the oncology market now valued at $55 billion, pharmaceuticals and biotech manufacturers are under pressure to find innovative ways of speeding development times in order to claim their share of

Venue: Le Meridien Piccadilly, London, UK

Validation of Computer Systems
From 26 April 2010 to 27 April 2010

Venue: Costa Mesa, CA

How to Implement Risk Management Principles and Activities within a Quality Management System
From 26 April 2010 to 27 April 2010

Venue: Costa Mesa, CA

The EU Clinical Trial Directive
From 26 April 2010 to 27 April 2010

Venue: Berlin, Germany

FDA Inspections of Clinical Data Systems
From 26 April 2010 to 27 April 2010

Venue: Dublin, Ireland

Cancer: Pathophysiology, Current Therapies, Clinical Trials and Drug Development
From 26 April 2010 to 28 April 2010

Venue: Washington, DC USA

Clinical Trial Planning and Management
From 26 April 2010 to 27 April 2010

Venue: Arlington, VA USA

CLINICAL AND POST MARKETING SAFETY
From 26 April 2010 to 27 April 2010

Venue: The Rembrandt Hotel, London

SUCCESSFUL IMPLEMENTATION OF MANUFACTURING SITE TRANSFERS
From 27 April 2010 to 28 April 2010
Considerations, Problems and Solutions - How to get it Right - A Practical Guide

Venue: The Rembrandt Hotel, London

Vaccine Innovation
From 27 April 2010 to 29 April 2010
New technological advances in vaccine research and development to revolutionise the industry

Venue: Frankfurt

Optimizing Brand Lifecycle Management Strategies
From 27 April 2010 to 27 April 2010
by Neal Hansen

Venue: Hilton Zurich Airport Hotel

Potency determination of drugs and biologics: design, and development of reliable potency bioassays
From 27 April 2010 to 27 April 2010
This potency bioassays training will helps you in understanding how to design and development of assays to measure potency, key validation parameters, and specifications. Problems due to method variab

Venue: Online Event

LogiPharma 2010
From 27 April 2010 to 29 April 2010
LogiPharma Europe is the Biggest and Most Senior Pharma Supply Chain Conference

Venue: Intercontinental Hoetl, Geneva

Pharmaceutical Marketing for Non-Marketers
From 27 April 2010 to 27 April 2010

Venue: Beaumont House, Windsor

SFE Europe 2010
From 27 April 2010 to 29 April 2010
Change Your Pharma Sales Force

Venue: Barcelona Spain

IN-VITRO DIAGNOSTICS - Part of the Medical Device Training Academy Series
From 27 April 2010 to 27 April 2010

Venue: MWB Business Exchange, Fleet Street, London EC4A

How to Prepare for Pharmacovigilance - Audits and Inspections in Europe
From 27 April 2010 to 27 April 2010

Venue: Paris France

Essentials of Program, Project & Portfolio Management in Bio/Pharmaceutical Discovery
From 28 April 2010 to 29 April 2010

Venue: Malvern, PA, USA

Phase IV Trials now Mandated by the FDAAA: What do they tell us?
From 28 April 2010 to 28 April 2010
This Phase IV Trials training will helps you in understanding FDA's mandate on Phase IV trial and best practices for successful studies that meet the complex requirements.

Venue: Online Event

Understanding Clinical Trials Regulations in Latin America
From 28 April 2010 to 28 April 2010
This Clinical Trials Regulations in Latin America training will review the applicable Regulatory Process in the main Latin American countries where Clinical Research is developed, identifying opportun

Venue: Online Event

Controlled Release
From 28 April 2010 to 29 April 2010

Venue: Crowne Plaza Hotel - St James, London

Understanding & Working with the NHS
From 28 April 2010 to 28 April 2010

Venue: Beaumont House, Windsor

ANCILLARY MEDICINAL SUBSTANCES - Part of the Medical Device Training Academy Series
From 28 April 2010 to 28 April 2010

Venue: MWB Business Exchange, Fleet Street, London EC4A

European Filing & Registration Procedures
From 28 April 2010 to 29 April 2010

Venue: Berlin, Germany

Dermatological Product Development
From 28 April 2010 to 29 April 2010

Venue: Malvern, PA, USA

Evolving Regulatory expectation for Particulates in Biologics
From 29 April 2010 to 29 April 2010
This webinar addresses evolving regulatory requirements for particulates and the techniques suitable for testing and characterizing sub-visible particulates in therapeutic formulations.

Venue: Online Event

The FDA's New Emphasis on Supplier Controls? Is Your Company Ready?
From 29 April 2010 to 29 April 2010
This presentation will detail the expectations and the details of the new GHTF guidance document on "the Controls of Products and Services Obtained from Suppliers" published in December 2008 and also

Venue: Online Event

The Pharma Business Development Course
From 29 April 2010 to 30 April 2010
By Martin Austin

Venue: Hilton Zurich Airport Hotel

Effective Sales Forecasting
From 29 April 2010 to 29 April 2010

Venue: Beaumont House, Windsor

OWN BRAND LABELLING, PROCEDURE PACKS AND SYSTEMS
From 29 April 2010 to 29 April 2010
Part of the Medical Device Training Academy Series

Venue: MWB Business Exchange, Fleet Street, London EC4A

Train The Pharmaceutical Trainer
From 29 April 2010 to 30 April 2010

Venue: The Rembrandt Hotel, London

New Drug Product Development & Lifecycle Management
From 29 April 2010 to 30 April 2010

Venue: Horsham, PA USA

MANAGING MEDICAL DEVICE SOFTWARE PROJECTS - Part of the Medical Device Training Academy Series
From 30 April 2010 to 30 April 2010

Venue: MWB Business Exchange, Fleet Street, London EC4A

Improving Immunohistochemistry - 2010
From 30 April 2010 to 30 April 2010

Venue: UCL Institute of Child Health, Kennedy Lecture Theatre, 30 Guilford Street, London WC1N 1EH, United Kingdom.

Drug Safety Surveillance and Epidemiology
From 03 May 2010 to 05 May 2010

Venue: Horsham, PA USA

cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
From 03 May 2010 to 05 May 2010

Venue: Costa Mesa, CA

Global Pharmacovigilance Training Course
From 03 May 2010 to 05 May 2010

Venue: Arlington, VA USA

Drug Development Decisions: The NDA Simulation Workshops
From 03 May 2010 to 05 May 2010

Venue: Arlington, VA USA

Latin America - Understanding Regulatory Compliance Requirements
From 04 May 2010 to 05 May 2010

Venue: Malvern, PA, USA

Software Development for Medical Device Professionals
From 04 May 2010 to 05 May 2010

Venue: Malvern, PA, USA

Essentials of Clinical Study Management
From 05 May 2010 to 07 May 2010

Venue: Vienna Austria

Introduction to Signal Detection and Data Mining
From 05 May 2010 to 05 May 2010

Venue: Horsham, PA USA

RAPS' Preparing Compliant eCTD Submissions Workshop
From 05 May 2010 to 07 May 2010
RAPS' Preparing Compliant eCTD Submissions Workshop: Master the eCTD for Europe and the US

Venue: Brussels

Essentials of Clinical Study Management
From 05 May 2010 to 07 May 2010

Venue: Hotel Austria Trend Savoyen | Vienna | Austria

Epilepsy: An Overview
From 05 May 2010 to 06 May 2010
Epilepsy: An Overview

Venue: London

Understanding The Competition
From 05 May 2010 to 05 May 2010

Venue: Beaumont House, Windsor

RNA & miRNA Congress
From 05 May 2010 to 07 May 2010

Venue: Boston, MA, USA

First Recruitment and Retention Conference.
From 05 May 2010 to 06 May 2010

Venue: Rockville, MD

Epigenetics World Congress
From 06 May 2010 to 07 May 2010

Venue: Boston, MA, USA

How to Prepare for a Safety Inspection
From 06 May 2010 to 06 May 2010

Venue: Horsham, PA USA

Risk Management and Communication to Optimize Medicinal Product Safety
From 06 May 2010 to 07 May 2010

Venue: Horshm, PA USA

Effective Laboratory Safety Management
From 06 May 2010 to 07 May 2010

Venue: Malvern, PA, USA

Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
From 06 May 2010 to 07 May 2010

Venue: Malvern, PA, USA

Pharmaceutical and Biopharmaceutical Quality Control Laboratories - A Regulatory Compliance Primer
From 06 May 2010 to 07 May 2010

Venue: Costa Mesa, CA

Principles and Practices of Traceability and Calibration
From 06 May 2010 to 06 May 2010
In this Calibration training learn and understand different types of measurements units, measurement constants, calibration and measurement standards as well as principles and practices of traceabilit

Venue: Online Event

7th Scientific & Technical Forum
From 06 May 2010 to 07 May 2010
Challenges and solutions for the formulation of classical and biological drugs

Venue: Hotel Bildungszentrum 21 - Basel/Switzerland

LATEST DEVELOPMENTS IN PHARMACOVIGILANCE
From 06 May 2010 to 07 May 2010

Venue: The Rembrandt Hotel, London

Genomics Automation Congress
From 06 May 2010 to 07 May 2010

Venue: Boston, MA, USA

INTRODUCTION TO THE MEDICAL DEVICE DIRECTIVE
From 06 May 2010 to 07 May 2010

Venue: Hotel to be Advised, London

Experimental Design and Practical Data Analysis in Positron Emission Tomography
From 07 May 2010 to 09 May 2010
Course: Experimental Design and Practical Data Analysis in Positron Emission Tomography

Venue: MRC Clinical Sciences Centre, Hammersmith Hospital Campus, W12 0NN London, UK

3rd Annual Regulatory Conference on "Global Regulatory Challenges: Quest for Optimization
From 07 May 2010 to 09 May 2010

Venue: Mumbia, India

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