Sep 2- Sep 3 | Effective Clinical Site Management & Patient Making an impact to your bottomline by improving processes and achieving greater efficiencies in clinical trials through effective site management & patient recruitment |  |
Sep 5- Sep 6 | The RPS conference 2010: Supporting patient and professional decision making Brand new conference |  | Sep 6- Sep 8 | LogiPharma China China’s Leading Pharmaceutical Supply Chain & Logistics Conference |  | Sep 8- Sep 9 | Pharmaceutical Distribution 2010 Pharmaceutical Distribution |  | Sep 8- Sep 9 | Global Pharmaceutical Project and Portfolio Management Forum
|  | Sep 8- Sep 10 | Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
|  | Sep 8- Sep 10 | Introduction to Molecular Biology Techniques
|  | Sep 9- Sep 10 | Preparing the CMC Section for NDAs/CTDs/INDs
|  | Sep 13- Sep 14 | Medical Approach in Diagnosis and Management of ADRs
|  | Sep 13- Sep 14 | Clinical Statistics for Nonstatisticians
|  | Sep 13- Sep 15 | Regulatory Affairs Part I: The IND Phase
|  | Sep 13- Sep 16 | World Pharma Trials Asia 2010 World Pharma Trials Asia 2010 |  | Sep 13- Sep 17 | Thirteenth Annual Land O’Lakes Conference on Drug Metabolism/Applied Pharmacokinetics
|  | Sep 13- Sep 14 | Clinical Statistics for Nonstatisticians
|  | Sep 13- Sep 16 | World Pharma Trials Asia 2010
|  | Sep 14- Sep 15 | 2nd Successful eCTD Lifecycle Management Pharma IQ is delighted to announce the 2nd Successful eCTD Lifecycle Management conference, being held in Prague on the 14th and 15th of September 2010 |  | Sep 14- Sep 17 | Health Network Communications Addressing the key challenges for safety professionals |  | Sep 14- Sep 17 | Antibody Development & Manufacturing Discover radical new approaches and technologies to transform your antibody production |  | Sep 14- Sep 15 | MEDICAL DEVICE CLINICAL STUDIES Understand How to Conduct Clinical Investigations and Post Market Clinical Follow-up for Medical Devices |  | Sep 14- Sep 14 | The role of Analytical Program to Support Drug Development Process 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 |  | Sep 15- Sep 16 | PHARMACEUTICAL PACKAGING AND LABELLING
|  | Sep 15- Sep 16 | Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
|  | Sep 15- Sep 16 | Financial Fundamentals for Non-Financial Personnel - How Financial Issues Impact Business
|  | Sep 15- Sep 17 | ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
|  | Sep 15- Sep 16 | Pharmaceutical Stability Testing Conference Pressure to ensure that the regulatory requirements for stability testing are fulfilled, first time has never been higher with the pharmaceutical industry as a whole focusing on cutting margins and av |  | Sep 15- Sep 16 | 8th Annual Pharmaceutical Technology IT Congress Spaces available - Don't miss out on this year's Pharma IT event |  | Sep 15- Sep 17 | 6th Annual Pharma Quality Management How to Achieve Quality and Process Excellence in Pharma? |  | Sep 15- Sep 16 | 8th Annual Pharmaceutical Technology IT Congress
|  | Sep 16- Sep 17 | Clinical Trials in Oncology
|  | Sep 16- Sep 17 | Clinical Trials in Oncology
|  | Sep 16- Sep 17 | Pharmaceutical Production Batch Record Review
|  | Sep 16- Sep 17 | Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
|  | Sep 16- Sep 17 | CNS Clinical trial CNS Clinical trial |  | Sep 17- Sep 19 | Quality of Active Pharmaceutical Ingredients
|  | Sep 19- Sep 22 | Asia Pacific Digestive Week 2010
|  | Sep 20- Sep 22 | Drug Safety Surveillance and Epidemiology
|  | Sep 20- Sep 22 | IIR's 2nd Annual Business of Biosimilars
|  | Sep 20- Sep 21 | Clinical Document Management – A Trial by Trial Approach to Compliance
|  | Sep 20- Sep 22 | CMC Regulatory Compliance for Biopharmaceuticals and Biologics
|  | Sep 20- Sep 21 | Labeling and Labeling Controls for Medical Devices
|  | Sep 20- Sep 21 | Validation of Computer Systems
|  | Sep 20- Sep 21 | ENVIRONMENTAL RISK ASSESSMENT OF HUMAN PHARMACEUTICALS
|  | Sep 20- Sep 22 | Innovation in Phase I Clinical Development Practical approaches to phase I trial development in order to enable faster go / no-go decisions, reduce cost and speed time to market |  | Sep 20- Sep 23 | 8th Annual Cold Chain Distribution for Pharmaceuticals Distributing Safe Medicines internationally in Collaboration with Temperature Control Partners and Stakeholders |  | Sep 21- Sep 22 | The International API GMP Guidance: ICH Q7 Implementation and Application
|  | Sep 21- Sep 22 | PHARMACOKINETICS In Drug Discovery and Development - INTERMEDIATE COURSE
|  | Sep 21- Sep 22 | Introduction to Medical Device Submissions – 510ks, PMAs, and Exemptions
|  | Sep 21- Sep 22 | Preparation of FDA Submissions and Communicating with the FDA
|  | Sep 21- Sep 22 | 2010 Pharma CI Conference The Best and Largest Gathering of Pharmaceutical Competitive Intelligence Professionals |  | Sep 21- Sep 23 | Influenza 2010: Zoonotic Influenza and Human Health |  | Sep 22- Sep 24 | Clinical Project Management in Europe - Part I
|  | Sep 22- Sep 23 | PHARMACEUTICAL ORIGINATION AND ARTWORK 2010
|  | Sep 22- Sep 23 | Biosimilars & Biobetters Aligning Business and Science for success |  | Sep 22- Sep 24 | Clinical Project Management in Europe - Part I
|  | Sep 22- Sep 22 | PHARMACEUTICALS AND LIFE SCIENCES STRENGTHS WORKSHOP DRIVING HIGH PERFORMANCE, ENGAGEMENT AND WELLBEING USING STRENGTHS-BASED HR IN PHARMACEUTICALS AND LIFE SCIENCES |  | Sep 22- Sep 24 | ADVANCED PHARMACOVIGILANCE
|  | Sep 22- Sep 24 | SUCCESSFUL MEDICAL WRITING
|  | Sep 22- Sep 23 | Software Development for Medical Device Professionals
|  | Sep 22- Sep 23 | Purchasing Controls in the Medical Device Industry
|  | Sep 22- Sep 24 | Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
|  | Sep 22- Sep 24 | BIOTECHNOLOGY FOR THE NON-BIOTECHNOLOGIST
|  | Sep 23- Sep 24 | Introduction to Medical Combination Products
|  | Sep 23- Sep 24 | Stability Programs for Product Shelf Life - From Development to Approval
|  | Sep 23- Sep 24 | Best Practices for Facilities and Utilities Design, Qualification and Monitoring
|  | Sep 23- Sep 24 | ABRIDGED LICENCE APPLICATIONS - Generics, Well Established Use & Mixed Product Licences
|  | Sep 23- Sep 24 | Building the eCTD: Practical Solutions to Compile Electronic Submissions
|  | Sep 23- Sep 24 | Building the eCTD
|  | Sep 24- Sep 24 | Miniaturisation - Micro Scale Bioprocess Development
|  | Sep 27- Sep 30 | Predictive In Vitro Models in Drug Development Accelerate preclinical drug development by accurately predicting in vivo safety and pharmacokinetics |  | Sep 27- Sep 28 | Amorphous Pharmaceutical Materials 2010 Achieving Commercial Success through the Implementation of Amorphous Techniques |  | Sep 27- Sep 29 | ELNs & Advanced Laboratory Solutions Increase your research efficiency, accelerate workflow and enhance geo-separate collaboration by establishing a clear e-laboratory environment in your company |  | Sep 27- Sep 27 | THE BORDERLINE BETWEEN MEDICINES AND FOODS
|  | Sep 27- Sep 29 | ELNs & Advanced Laboratory Solutions Increase your research efficiency, accelerate workflow and enhance geo-separate collaboration by establishing a clear e-laboratory environment in your company |  | Sep 27- Sep 28 | Good Laboratory Practices (GLP) for Pre-Clinical Testing
|  | Sep 27- Sep 28 | Best Practices for an Effective Cleaning Validation Program
|  | Sep 27- Sep 28 | Writing Effective Standard Operating Procedures and Other Process Documents
|  | Sep 27- Sep 28 | Adverse Drug Events – Reporting & Regulatory Requirements
|  | Sep 27- Sep 28 | Design Control for Medical Device Professionals
|  | Sep 27- Sep 28 | Pharmaceutical Co-Crystals 2010 Realising the Commercial Potential of Implementing Pharmaceutical Co-Crystals into Your R&D Strategy |  | Sep 27- Sep 28 | Clinical Statistics for Nonstatisticians
|  | Sep 27- Sep 29 | Workshop on Statistical Methodology in Clinical R&D
|  | Sep 27- Sep 28 | FDA APPROVAL PROCESS FOR MEDICAL DEVICES
|  | Sep 28- Sep 29 | e-Patient Connections 2010 Health Communications, Marketing, Education |  | Sep 28- Oct 1 | Digipharm Europe 2010 Meeting the world's most exclusive pharmaceutical brands |  | Sep 28- Sep 29 | The EU Clinical Trial Directive
|  | Sep 28- Sep 29 | Executing Global Clinical Trial Operations Conference How to Globalize your Study for Clinical Success |  | Sep 28- Sep 29 | Global Clinical Trials Best practices to globalize your study for clinical success |  | Sep 28- Sep 30 | Computational Drug Research and Development Do IT and R&D work together as well as they should in your organization? |  | Sep 28- Sep 29 | Joint EFGCP Children's Medicine Working Party 6th Annual Conference and DIA 4th Paediatric Forum
|  | Sep 29- Sep 30 | KOL: Knowledge Leader Partnerships Recruitment, Management, Transparency & Future |  | Sep 29- Oct 1 | Good Manufacturing Practices
|  | Sep 29- Oct 1 | The Drug Development Process - From Discovery to Commercialization
|  | Sep 29- Sep 30 | Process Validation for Drugs and Biologics
|  | Sep 29- Sep 30 | Design Validation, Verification, and Risk Analysis for Medical Device Professionals
|  | Sep 29- Sep 30 | QUALITY BY DESIGN: ON A SMALL BUDGET - A Cost Effective Approach to Practical Implementation
|  | Sep 29- Sep 30 | Advanced Clinical Statistics for Non-Statisticians
|  | Sep 29- Sep 29 | FDA REQUIREMENTS FOR COMBINATION PRODUCTS
|  | Sep 30- Oct 1 | Global Approach to the Risk Management of Medicines
|  | Sep 30- Oct 1 | European Filing & Registration Procedures
|  | Sep 30- Oct 1 | Effective Document Management for Pharmaceutical, Biotech, & Medical Device Industries
|  |