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Events

Featured Events

Translational Neuroscience

27 Oct 10 - 28 Oct 10

Biorbis

The treatment of neurological disorders has entered a new period of optimism. New insights into the underlying mechanisms of previously untreatab...

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FT Pharmaceutical & Biotechnology Conference 2010

01 Dec 10 - 02 Dec 10

Financial Times

Chaired by Andrew Jack, Pharmaceuticals Correspondent of the Financial Times, the FT Global Pharmaceutical and Biotechnology Conference, now in its...

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Partnerships in Pharma

01 Oct 10 - 01 Oct 10

Economist Conferences

Successful collaborations depend on a multitude of critical factors, all of which will be explored at the Economist Intelligence Unit’s Partn...

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Multi Channel Pharma Marketing Event

13 Oct 10 - 14 Oct 10

The Multi Channel Pharma Marketing Event Team

Brought to you by the producers of the sold out ePharma Summit, the Multi Channel Pharma Marketing Event brings together product managers and marke...

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Effective Clinical Site Management & Patient

02 Sep 10 - 03 Sep 10

Marcus Evans

Owing to her vast practical experience, the courser facilitator has the ability to package and present training material in a manner that gives att...

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BioManufacturing World

18 Oct 10 - 21 Oct 10

Imapac Pte Ltd

BioManufacturing World 2010 is the largest global conference in China that gather international and Chinese biopharmaceutical manufacturers, CMOs, ...

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Global Pharmaceutical Project and Portfolio Management Forum

08 Sep 10 - 09 Sep 10

Event Associates International Ltd

This Global forum will cater for approximately 100 to 150 executives, drawn from leading pharmaceutical companies world wide, who are all looking to n...

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6th Annual Pharma Quality Management

15 Sep 10 - 17 Sep 10

Jacob Fleming

What are the best practices to achieve QC Laboratory Excellence? How successful are you in adopting and sustaining consistent, harmonized & compl...

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To feature your event in this list email editor@pharmiweb.com

All Events

June 2010

Jun 9- Mar 23	3rd DIA Regulatory Affairs Training Course
Jun 16- Jun 18	10th Annual BioDundee International Conference 10th BioDundee International Conference 2010

January 2012

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	Event is based in the UK
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	Event is based world wide

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PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings. The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.

Jul 12- Jul 11	Clinical Pharmaceutical Core Program
Jul 12- Jul 12	GMP Pharmaceutical Core Program
Jul 12- Jul 12	Validation and Part 11 Compliance
Jul 31- Aug 3	BIT’s 1st World Congress of Virus and Infections-2010 Voice of Virologists

Aug 2- Aug 5	International Intellectual Property Law Summer School A 3-day fully residential programme for lawyers and executives working in international business who need to develop their knowledge of all aspects of international intellectual property law
Aug 2- Aug 12	Leadership Experience
Aug 3- Aug 4	Selecting and Managing CRO's
Aug 5- Aug 6	Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
Aug 5- Aug 6	Medical Management in Medicare Advantage: A Payer/Provider Collaborative Care Summit
Aug 5- Aug 6	Medical Management in Medicare Advantage:Payer/Provider Collaborative Care Summit
Aug 7- Aug 8	Pharmaceutical Quality Forum: CMC Compliance
Aug 9- Aug 10	Latin America - Understanding Regulatory Compliance Requirements
Aug 9- Aug 10	How to Develop an Effective Complaint Handling, and Post Market Surveillance Program
Aug 9- Aug 11	Cost Contained Regulatory Compliance for the Drug, Biologics and Medical Device Industries
Aug 9- Aug 11	PHARMACOKINETICS: Essential Theory and Practical Considerations
Aug 9- Aug 13	Regulatory Affairs Part I: The IND Phase and Part II: The NDA Phase
Aug 9- Aug 10	European Regulatory Affairs
Aug 10- Aug 11	Auditing and Qualifying API Suppliers
Aug 11- Aug 12	Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Aug 11- Aug 13	Root Cause Analysis for CAPA
Aug 16- Aug 17	FDA Inspections - What to Expect and How to Prepare
Aug 16- Aug 17	Adverse Drug Events – Reporting & Regulatory Requirements
Aug 16- Aug 17	Writing Effective Standard Operating Procedures and Other Process Documents
Aug 17- Aug 18	Process Validation Workshops for pharmaceutical
Aug 17- Aug 18	The International API GMP Guidance: ICH Q7 Implementation and Application
Aug 18- Aug 19	Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
Aug 18- Aug 20	The Drug Development Process - From Discovery to Commercialization
Aug 19- Aug 20	Writing in the Regulated Environment When English Is Your Second Language
Aug 19- Aug 20	NDDS India 2010: Novel Drug Delivery Systems Leveraging technological advances in novel drug delivery systems
Aug 23- Aug 24	Good Clinical Practice for Medical Device Investigations
Aug 23- Aug 24	Pharmaceutical and Biopharmaceutical Quality Control Laboratories
Aug 23- Aug 24	2nd annual drug discovery: Easing the bottleneck
Aug 23- Aug 24	Drug Discovery: Easing the Bottleneck
Aug 24- Aug 25	Artillery Systems Asia The First and Only Dedicated Artillery Systems Conference in Asia!
Aug 24- Aug 26	Advancing Clinical Trials in Oncology Understanding the Effective Design and Execution of Oncology Clinical Trials
Aug 25- Aug 27	cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
Aug 25- Aug 26	Good Clinical Practice Auditing
Aug 28- Sep 1	Infectious Disease 2010 Board Review Course Infectious Disease 2010 Board Review Course-15th Annual Comprehensive Review for Board Preparation
Aug 28- Aug 29	Balanced Scorecard Certification Workshop Get Balanced Scorecard Certified
Aug 30- Aug 31	Detecting Fraud and Misconduct in Clinical Trials

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

Oct 1- Oct 1	Partnerships in Pharma
Oct 1- Oct 1	Joint DIA/EFGCP Pharmacovigilance Audit and Inspection - Opportunities for Patient Safety
Oct 1- Oct 1	Joint DIA / EFGCP Pharmacovigilance Audit and Inspection Workshop Opportunities for Patient Safety
Oct 1- Oct 1	Non-coding RNAs in development
Oct 3- Oct 4	Project Management for the Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
Oct 3- Oct 5	Optimization of Drug-Like Properties in Drug Discovery
Oct 3- Oct 5	Spectroscopic Method Development for the Pharmaceutical and Biotech Industries
Oct 4- Oct 5	The Pharma Brand Planning Course by Edouard Demeire
Oct 4- Oct 6	Tablets & Capsules - Development, Manufacture and Testing of Solid Oral Dosage Forms
Oct 4- Oct 5	Validation of Computer Systems
Oct 4- Oct 5	Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
Oct 4- Oct 5	Practical Methods for Project Management
Oct 4- Oct 5	Patent and Other Intellectual Property Law for the Life Sciences Industry
Oct 4- Oct 5	Managing Partnerships with CROs
Oct 4- Oct 6	Regulatory Affairs Part II: The NDA Phase
Oct 4- Oct 5	4th Annual Pain Therapeutics Summit
Oct 4- Oct 8	Practical Strategies for Developing Preclinical and Phase 1 Oral Drug Formulations
Oct 4- Oct 4	AN ESSENTIAL GUIDE TO PHARMACOVIGILANCE
Oct 5- Oct 6	International Diabetes Summit
Oct 5- Oct 5	THE CLINICAL OVERVIEW AND CLINICAL SUMMARY Creating an Effective Marketing Authorisation Application
Oct 5- Oct 6	Development of Type 2 Diabetes Mellitus Drugs: State of the Art Cardiovascular Safety Assessments
Oct 5- Oct 6	Haematological Malignancies Haematological Malignancies
Oct 5- Oct 6	Effective Quality Assurance Auditing for FDA Regulated Industries
Oct 5- Oct 6	The EU Clinical Trial Directive
Oct 6- Oct 8	Practical GCP Compliance Auditing of Trials & Systems
Oct 6- Oct 8	Practical GCP Compliance Auditing of Trials & Systems
Oct 6- Oct 6	International Diabetes ?Summit
Oct 7- Oct 8	Utilizing Chemistry, Manufacturing & Control (CMC) in Drug Development
Oct 7- Oct 7	Induced pluripotent stem cells: production and utility in regenerative medicine
Oct 7- Oct 8	Quality System Regulation for the Medical Device & Biotech Industries
Oct 7- Oct 8	Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
Oct 7- Oct 8	European Filing & Registration Procedures
Oct 7- Oct 8	How to Implement Risk Management Principles and Activities within a Quality Management System
Oct 7- Oct 8	The Pharma Forecasting Course by Gary Johnson
Oct 7- Oct 8	3rd Pharma Marketing and Sales Force Strategies Reformulating marketing and sales to optimise ROI and drive future growth
Oct 8- Oct 8	Discussion Workshop: Improving immunohistochemistry 2010
Oct 11- Oct 12	FDA Inspections - What to Expect and How to Prepare
Oct 11- Oct 12	How to Monitor Clinical Trials for GCP Compliance
Oct 11- Oct 12	Medical Devices - EU Directives, Guidance, CE Marking and ISO Standard Certifications
Oct 11- Oct 13	4th Annual Clinical Forum 2010
Oct 11- Oct 11	REGULATORY AFFAIRS FOR SUPPORT STAFF ~ PART 1 An Overview of Pharmaceutical Regulatory Affairs For Support Staff
Oct 11- Oct 11	TECHNICAL FILE DOCUMENTATION AND REVIEW - Part of the Medical Device Training Academy Series
Oct 12- Oct 12	REGULATORY AFFAIRS FOR SUPPORT STAFF ~ PART 2 A Continuation Course
Oct 12- Oct 12	RISK MANAGEMENT FOR MEDICAL DEVICES - Part of the Medical Device Training Academy Series
Oct 12- Oct 13	DISTRIBUTION OF MEDICINES - FROM GOOD PRACTICE TO BEST PRACTICE: The New European Guidelines
Oct 12- Oct 15	The 4-day Mini-Masters for Pharma, Biotech & Life Sciences A 4-day ‘Mini-Masters’ programme developing the skills of key executives and managers in the pharma/bio-tech/life sciences sector.
Oct 12- Oct 13	Marketing, Advertising and Promotion of Pharmaceuticals and Medical Devices
Oct 13- Oct 14	Maternal and Pediatric Drug Safety Symposium
Oct 13- Oct 14	Detecting Fraud & Misconduct in Clinical Trials
Oct 13- Oct 15	Process Validation for Medical Devices
Oct 13- Oct 15	QA/QC Strategy for Biopharmaceuticals and Biologics
Oct 13- Oct 14	Making the Right Investments in Biomedical Informatics for Drug Development and Healthcare
Oct 13- Oct 14	Early Drug Development: Navigating the Treacherous Rapids
Oct 13- Oct 13	SUPPLIER MANAGEMENT AND PURCHASING CONTROLS FOR MEDICAL DEVICES AND IVDs Part of the Medical Device Training Academy Series
Oct 13- Oct 14	Investing in Biomedical Informatics for Drug Development and Health Care
Oct 13- Oct 14	Multi Channel Pharma Marketing Event
Oct 14- Oct 15	Partnerships to Advance Patient Recruitment and Retention in Clinical Research DIA and FDA Office of Women’s Health OWH
Oct 14- Oct 14	MANAGING MEDICAL DEVICE SOFTWARE PROJECTS Part of the Medical Device Training Academy Series
Oct 14- Oct 14	THE ROLE OF THE RESPONSIBLE PERSON
Oct 14- Oct 14	INTRODUCTION TO PUBLICATION PLANNING AND STRATEGY
Oct 14- Oct 14	THE ROLE OF THE RESPONSIBLE PERSON
Oct 14- Oct 15	Pharmaceutical Production Batch Record Review
Oct 15- Oct 15	ADVANCED PUBLICATIONS PLANNING
Oct 18- Oct 21	Leadership Experience
Oct 18- Oct 20	Essentials of Project Management
Oct 18- Oct 21	BioManufacturing World
Oct 18- Oct 19	SBS Biomolecular Screening Symposium Advanced Applications Across Academia, Government & Industry
Oct 18- Oct 19	BIOLOGICAL EVALUATION OF MEDICAL DEVICES Understand The New Approach To Biological Evaluation And Its Practical Application
Oct 18- Oct 19	PHARMACOKINETICS - Workshop for Beginners
Oct 18- Oct 21	Vaccine Manufacturing World
Oct 18- Oct 19	Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
Oct 18- Oct 20	Biostatistics for Non-Statisticians
Oct 18- Oct 19	BRIDGING THE REGULATORY GAP BETWEEN AUSTRALIA, NEW ZEALAND AND EUROPE
Oct 18- Oct 20	Joint DIA-ACT Study Director Workshop
Oct 19- Oct 19	The changing role of NICE
Oct 19- Oct 20	The Pharma Market Access Course by Lloyd Morgan and Konrad Wallerstein
Oct 19- Oct 22	Exploratory Clinical Development World USA 2010
Oct 19- Oct 20	New Drug Product Development & Lifecycle Management
Oct 19- Oct 21	Global Discovery Outsourcing and Collaborations Forum Pharma IQ is proud to announce Global Discovery Outsourcing and Collaborations Forum, held in London on the 20th – 21st October 2010
Oct 20- Oct 21	Infection: An Overview Infection: An Overview
Oct 20- Oct 20	PHARMACODYNAMICS
Oct 20- Oct 21	DRUG / DEVICE & DEVICE / DRUG COMBINATIONS IN THE EU
Oct 20- Oct 22	CMC Regulatory Compliance for Biopharmaceuticals and Biologics
Oct 21- Oct 22	Essentials of Program, Project & Portfolio Management in Bio/Pharmaceutical Discovery
Oct 21- Oct 22	The Pharma Pricing Course for Pricing & Marketing Executives by Gary Johnson
Oct 21- Oct 22	Auditing and Qualifying Suppliers and Vendors
Oct 21- Oct 22	Introduction to Statistical Analysis of Laboratory Data
Oct 21- Oct 21	SCIENTIFIC ADVICE Optimising Regulatory Input Into Drug Development
Oct 21- Oct 21	Role of RNA structures in post-transcriptional control of gene expression
Oct 21- Oct 22	Executing and Controlling Projects
Oct 21- Oct 22	Enterprise Resource Planning
Oct 22- Oct 23	MENA Oncology Conference
Oct 23- Oct 26	BIT’s 8th Annual Congress of International Drug Discovery Science and Technology (IDDST) Supporting Systems for Major Innovative Drug
Oct 23- Oct 26	5th Annual Conference on Drug Discovery and Clinical Development
Oct 25- Oct 26	Best Practices for an Effective Cleaning Validation Program
Oct 25- Oct 26	Design Control for Medical Device Professionals
Oct 25- Oct 26	Effective Document Management for the Pharmaceutical, Biotech & Medical Device Industries
Oct 25- Oct 26	The Pharma Business Development Course by Martin Austin
Oct 25- Oct 26	REGULATORY AFFAIRS IN AFRICA including SOUTH AFRICA
Oct 25- Oct 26	4th DIA European Cardiac Safety Conference 4th DIA European Cardiac Safety Conference
Oct 25- Oct 26	4th European Cardiac Safety Conference
Oct 25- Oct 29	Excellence in Pharmacovigilance: Clinical Trials and Post Marketing
Oct 25- Oct 26	Nutraceuticals and Functional Foods
Oct 25- Oct 26	Point of Care Diagnostics Market Adoption and Technology Trends
Oct 25- Oct 26	Point of Care Diagnostics Market Adoption and Technology Trends
Oct 25- Oct 26	2nd annual medicare advantage strategic business symposium
Oct 25- Oct 26	5th Annual Generics Asia The Only Event in Asia to have truly substantial and relevant discussions on the hottest issues such as leveraging on brands, biosimilars, regulatory updates and collaboration opportunities between in
Oct 26- Oct 29	World Stem Cells and Regenerative Medicines Congress Asia 2010
Oct 26- Oct 27	STATISTICAL, CLINICAL, REGULATORY, AND ETHICAL FACTORS ENSURING QUALITY AND BALANCING RISKS FOR MULTIREGIONAL CLINICAL TRIALS
Oct 26- Oct 27	9th World Drug Discovery & Development Summit 2010
Oct 26- Oct 27	Pediatric Clinical Trial Design - Ethics, Management and Regulatory Requirements
Oct 26- Oct 27	Tomorrow's Project Manager: Evolving Competencies for Biopharmaceutical Professionals
Oct 27- Oct 28	Design Validation, Verification, and Risk Analysis for Medical Device Professionals
Oct 27- Oct 28	Process Validation for Drugs and Biologics
Oct 27- Oct 27	Optimizing Brand Lifecycle Management Strategies by Neal Hansen
Oct 27- Oct 28	Translational Neuroscience Providing the Bedrock for Clinical Progression
Oct 27- Oct 29	2010 Mid-Atlantic Bio Conference The Epicenter of Bioscience, Capital, and Policy
Oct 27- Oct 28	Introduction to Oncology and Chemotherapy
Oct 27- Oct 28	Medicaid business in focus: CFO Forum
Oct 27- Oct 28	European Pharmaceutical Pricing & Reimbursement
Oct 28- Oct 29	2nd annual drug discovery partnerships: filling the pipeline
Oct 28- Oct 29	he 9th Annual Electronic Submissions Conference: Working Together Towards a Global Strategy
Oct 28- Oct 29	7th DIA Japan Annual Meeting
Oct 28- Oct 29	An Introduction to Product Information Management (PIM)
Oct 28- Oct 28	Pharma-Biotech Product & Company Valuation by Patrik Frei and Johan Ohlsson
Oct 28- Oct 29	FDA Inspections of Clinical Data Systems
Oct 28- Oct 29	Introduction to Effective Medical Writing

Nov 1- Nov 2	Project Management for Phase 1 & 2 Clinical Trials
Nov 1- Nov 2	Medicare Advantage Strategic Business Symposium
Nov 1- Nov 2	Medicare advantages strategic Business symposium: Puerto Rico
Nov 2- Nov 3	Cold Chain & Logistics Management
Nov 2- Nov 2	MicroRNAs and their targets: promises and pitfalls A Biochemical Society Workshop
Nov 2- Nov 3	Cold Chain & Logistics Management
Nov 2- Nov 3	Preparation of FDA Submissions and Communicating with the FDA
Nov 2- Nov 3	Selecting and Managing CROs
Nov 2- Nov 3	Hospital Efficiency 2010 Reducing congestion and improving patient safety by streamlining work flow processes
Nov 3- Nov 3	Future Direction for Orphan Drugs in Europe Future Direction for Orphan Drugs in Europe
Nov 3- Nov 3	Future Direction for Orphan Drugs in Europe
Nov 3- Nov 5	“Keeping Canada on the Map: Fostering Innovation and Access to Drugs in Canada” DIA’s 8th Annual Canadian Meeting
Nov 3- Nov 4	Parkinson’s Disease Parkinson’s Disease
Nov 4- Nov 5	Second Health Technology Assessment (HTA) Conference
Nov 4- Nov 5	Second Health Technology Assessment (HTA) Conference Building a new System to get Effective Treatment to European Patients
Nov 4- Nov 5	Quality by Design: A Hands-on Short Course for Pharma
Nov 4- Nov 5	DIA/FDA Orphan Drug Designation Workshop
Nov 4- Nov 5	Understanding the Statistical Thinking in Clinical Research for Drug Development
Nov 4- Nov 5	Effective Laboratory Safety Management
Nov 4- Nov 5	Stability Programs for Product Shelf Life - From Development to Approval
Nov 5- Nov 5	Veterinary Allergy: Current Research and Diagnosis
Nov 8- Nov 10	Phacilitate CNS Leaders’ Forum 2010
Nov 8- Nov 10	Introduction to Good Clinical Practices and Auditing
Nov 8- Nov 8	DEVELOPING DPIs - Pre-Conference Workshop for N11-8010
Nov 8- Nov 10	PHARMACEUTICAL REGULATORY AFFAIRS IN LATIN AMERICA Regulatory Requirements for the Pharmaceutical
Nov 8- Nov 9	Cleanroom Microbiology for the Non-Microbiologist
Nov 9- Nov 9	Conference on Combination Products Finding the Right Regulatory Strategy
Nov 9- Nov 10	INHALED DRUG DELIVERY (IDD) - The Challenges and Opportunities of Bioequivalence
Nov 9- Nov 9	Pfizer Excellence in Oncology Awards 2010 Pfizer Excellence in Oncology Awards 2010
Nov 9- Nov 9	DRAFTING AND NEGOTIATING CLINICAL TRIALS AGREEMENTS
Nov 9- Nov 12	Oncology Clinical Experience Programme Oncology Clinical Experience Programme
Nov 10- Nov 11	GMP Auditor Training
Nov 10- Nov 11	Technology Transfer
Nov 10- Nov 12	Clinical Research Harmonization and the Future of Drug Development in Latin America 7th Latin American Congress
Nov 10- Nov 12	Good Management of Medical Devices
Nov 10- Nov 12	THE PHARMA MINI MBA ~ MANAGEMENT FORUM'S AUTUMN SCHOOL A 3 Day Accelerated Management Programme, with Residential Option
Nov 10- Nov 12	The Drug Development Process – From Discovery to Commercialization
Nov 10- Nov 11	Sterilization Procedures: Technology, Equipment & Validation
Nov 10- Nov 12	The CTD/eCTD: Building the Marketing Application throughout Clinical Development
Nov 11- Nov 12	Preparing the CMC Section for NDAs/CTDs/INDs
Nov 11- Nov 12	Pharmaceutical Serialisation and Traceability Effectively Tracing from Manufacture to Pharmacy
Nov 11- Nov 12	Regulatory Affairs in Biologics
Nov 11- Nov 12	Allosteric Modulator Congress
Nov 12- Nov 12	How to Audit API Manufacturers
Nov 12- Nov 12	Understanding dendritic cells and their ability to regulate immune responses
Nov 15- Nov 17	Clinical Project Management
Nov 15- Nov 16	Pre-marketing Clinical Safety & Pharmacovigilance
Nov 15- Nov 18	Regulatory Affairs Part I: The IND Phase and Part II: The NDA Phase
Nov 15- Nov 16	Pharmaceutical Packaging leadership summit
Nov 15- Nov 17	Good Clinical Practices (GCP)
Nov 15- Nov 16	Latin America - Understanding Regulatory Compliance Requirements
Nov 15- Nov 17	Preparing Compliant eCTD Submissions Workshop Master the eCTD for Europe and the US with this interactive workshop offered by the Regulatory Affairs Professionals Society (RAPS)
Nov 15- Nov 17	Preparing Compliant eCTD Submissions Workshop Master the eCTD for Europe and the US with this interactive workshop offered by the Regulatory Affairs Professionals Society (RAPS)
Nov 15- Nov 16	Clinical Trials in CNS
Nov 16- Nov 16	Multiple Sclerosis: An Overview
Nov 16- Nov 17	AN INTRODUCTION TO THE MEDICAL DEVICE DIRECTIVES
Nov 16- Nov 17	Health Economics for Non-Health-Economists by Lieven Annemans
Nov 16- Nov 17	Pharmaceutical Water Systems: Contemporary Technology & Compliance
Nov 16- Nov 18	World Generic Medicines Congress Americas 2010
Nov 16- Nov 17	The Science of BioBanking
Nov 17- Nov 18	Cardiovascular Medicine: An Overview Cardiovascular Medicine: An Overview
Nov 17- Nov 18	Post-marketing Drug Safety & Pharmacovigilance
Nov 17- Nov 18	COPD: Novel Therapeutics and Management Strategies
Nov 18- Nov 19	Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
Nov 18- Nov 19	Effective Risk-Based Applications of Drug cGMPs and Validation Req. for Cosmetics and OTC
Nov 18- Nov 19	Medical Devices Directives: Lessons Learned and the Way Forward Ensure that you and your company are compliant in response to the revised MDD
Nov 19- Nov 19	AN OVERVIEW OF THE eCTD - Are you up to date?
Nov 19- Nov 19	Introduction to Signal Detection and Data Mining
Nov 19- Nov 19	Flow Cytometry Instrumentation and techniques; keeping up with the Changes
Nov 22- Nov 24	Tabletting technology for the pharmaceutical industry
Nov 22- Nov 23	Cell Based Assays
Nov 22- Nov 22	PHARMACOKINETICS & DYNAMICS IN EARLY CLINICAL DEVELOPMENT 3 New training days to deliver high quality training for restricted budgets
Nov 23- Nov 23	DRUG SWITCHABILITY & POPULATION PK/PD PART OF THE PHARMACOKINETICS & PHARMACODYNAMICS TRAINING DAYS 2010 - 3 New training days to deliver high quality training for restricted budgets
Nov 23- Nov 24	The Pharma Forecasting Course by Gary Johnson
Nov 23- Nov 23	Joint DIA/EMA Variations Conference
Nov 24- Nov 24	TOXICOLOGY PART OF THE PHARMACOKINETICS & PHARMACODYNAMICS TRAINING DAYS 2010 - 3 New training days to deliver high quality training for restricted budgets
Nov 24- Nov 25	Introduction to Oncology and Chemotherapy
Nov 25- Nov 26	The Pharmaceutical Out-licencing Course by David Scott
Nov 29- Nov 30	2nd Joint DIA/ European Medicines Agency Innovation Forum: Is the EU Regulatory Framework Ready?
Nov 29- Nov 30	Pharmaceutical License Event PharmaVenue Unparalleled opportunities for establishing new business relationships with companies through one-to-one meetings.
Nov 29- Nov 30	MEDDRA & PHARMACOVIGILANCE
Nov 30- Dec 1	Health Economics for Pharmaceutical Personnel
Nov 30- Dec 2	World Drug Manufacturing Increasing innovation and reducing costs across global operations.
Nov 30- Dec 1	The Pharma Business Development Course by Martin Austin
Nov 30- Dec 1	Selecting and Managing CROs

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Translational Neuroscience

FT Pharmaceutical & Biotechnology Conference 2010

Partnerships in Pharma

Multi Channel Pharma Marketing Event

Effective Clinical Site Management & Patient

BioManufacturing World

Global Pharmaceutical Project and Portfolio Management Forum

6th Annual Pharma Quality Management

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January 2012

Dec 1- Dec 3	Technical Writing for Pharmaceutical, Medical Device and Biotech Industries
Dec 1- Dec 3	Good Manufacturing Practices
Dec 1- Dec 2	FT Pharmaceutical and Biotechnology conference 2010 Catching the Next Wave
Dec 1- Dec 3	11th Conference on European Electronic Document Management
Dec 1- Dec 2	LogiPharma Asia 2010 LogiPharma Asia examines the top SCM/logistics issues and challenges of the pharmaceutical industry in Asia.
Dec 1- Dec 2	FT Pharmaceutical & Biotechnology Conference 2010 Catching the Next Wave
Dec 1- Dec 3	Practical Guide for Pharmacovigilance: Clinical Trials and Post Marketing
Dec 2- Dec 3	SUCCESSFUL PHARMA PROJECT MANAGEMENT
Dec 2- Dec 2	Breast Cancer: Treatment and Management Breast Cancer: Treatment and Management
Dec 2- Dec 5	14th Asia-Oceania Congress of Endocrinology
Dec 2- Dec 3	The Digital Pharma Marketing Course by Fonny Schenck
Dec 2- Dec 3	Clinical Trial Design for Medical Devices
Dec 2- Dec 3	Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
Dec 2- Dec 3	Preparation of FDA Submissions and Communicating with the FDA
Dec 5- Dec 7	CTD Dossier Requirements: Focus on EU Module 1 and Quality Module 3
Dec 6- Dec 7	ESSENTIAL GUIDE TO CLINICAL TRIAL REGULATIONS
Dec 6- Dec 7	MEDICAL DEVICE REGULATIONS IN ASIA / PACIFIC MARKETS
Dec 6- Dec 8	cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
Dec 6- Dec 7	Stability Programs for Product Shelf Life - From Development to Approval
Dec 6- Dec 8	BioPharma India Convention 2010
Dec 7- Dec 9	BIT’s 2nd Annual International Congress of Cardiology Translational Medicine to Healthcare
Dec 8- Dec 10	Root Cause Analysis for CAPA
Dec 8- Dec 9	Software Development for Medical Device Professionals
Dec 8- Dec 10	The CTD/eCTD: Building the Marketing Application throughout Clinical Development
Dec 8- Dec 8	Overview of Drug Development
Dec 9- Dec 9	eCTD Submissions in Switzerland
Dec 9- Dec 10	FDA INSPECTIONS FOR MEDICAL DEVICES Is Your Company Prepared?
Dec 13- Dec 15	PHARMACOVIGILANCE A Basic Training Course For Those Working On Drug Safety Monitoring In The EU, USA And Japan
Dec 13- Dec 14	Good Clinical Practice for Medical Device Investigations
Dec 13- Dec 14	Overview of FDA Regulatory Compliance for Medical Devices
Dec 15- Dec 16	Good Clinical Practice Auditing
Dec 21- Dec 22	Diabetes and Diabetic Retinopathy Conference Diabetes and Diabetic Retinopathy

Feb 11- Feb 11	Bioethanol in the UK: Challenges & Opportunities
Feb 11- Feb 12	Conference On Indian Medical Devices & Plastics Disposables Industry 2011 Conference On Indian Medical Devices & Plastics Disposables Industry 2011
Feb 24- Feb 24	The Global Public Health implications of Tropical Diseases Research

Mar 10- Mar 10	Identifying T Cell Subset Phenotype and Function in Infections
Mar 11- Mar 11	Identifying T cell subsets in Autoimmunity
Mar 30- Apr 1	16th Congress of the European Association of Hospital Pharmacists Congress Focus: Hospital Pharmacists in a changing world - opportunities and challenges.