Events Calendar
Welcome to the Pharmaceutical Online Events Calendar!
Use this page to view Upcoming Events, jump to Advanced Search, or begin to Post Events.
Events By Name
Enter the event name in the form below and click on the search button to obtain event information. For a more powerful search with additional filters, try our Advanced Search.
Upcoming Events
- May 24, 2012 - An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials
- May 24, 2012 - Advances in Pharmaceutical Processing
- May 24, 2012 - Pre-Approval Statements and Representations by Pharmaceutical Manufacturers
- May 24 - 25, 2012 - Non-Antibody Protein Production
- May 24 - 25, 2012 - Statistics for the Non-Statistician - US Seminar 2012 at Washington DC
Events By Month
Click on a month below to view its associated events.
May 2012 [+] (70 total)
-
Best Practices For An Effective Cleaning Validation Program
May 1 - 2, 2012
Los Angeles CA US
Read more... -
Root Cause Analysis of Failures & Deviations - Developing an Effective CAPA Strategy
May 2 - 4, 2012
King of Prussia PA US
Read more... -
Raw Materials Risk Management in GMP Facilities: Avoiding GMP non-Compliance Due to Raw Material Issues
May 3, 2012
Palo Alto CA US
Read more... -
Validation and 21 CFR Part 11 Compliance of Computer Systems - US Seminar 2012 at San Francisco
May 3 - 4, 2012
San Francisco, Marriott Marquis Downtown ,8 AM PDT CA US
Read more... -
Medical Device Quality Systems, CAPA and European Medical Device regulations
May 3 - 4, 2012
Tampa FL US
Read more... -
Process Validation for Drugs and Biologics
May 3 - 4, 2012
Los Angeles CA US
Read more... -
Validation of Computer Systems
May 7 - 8, 2012
Berlin DE
Read more... -
Calibration and Qualification in Analytical Laboratories,
May 8, 2012
Palo Alto CA US
Read more... -
FDA Software Validation Self-Check – plan an effective Internal Audit program
May 9, 2012
Palo Alto CA US
Read more... -
Filing Variations
May 9 - 10, 2012
Brussels BE
Read more... -
Licensing for Pharmaceuticals and Biopharmaceuticals
May 9 - 10, 2012
Brussels BE
Read more... -
Process Analytical Technology (PAT) is more than it Seems - US Seminar 2012 at San Francisco
May 10 - 11, 2012
San Francisco, Marriott Marquis Downtown 8 AM PDT CA US
Read more... -
Decoding CLIA (Clinical Laboratory Improvement Amendments) Regulations: Calibration, Calibration Verification and Method Validation
May 10, 2012
Palo Alto CA US
Read more... -
Key GMP Systems in Pharmaceutical and Biotech Labs
May 10 - 11, 2012
Boston MA US
Read more... -
Six Sigma Green Belt Certification Training
May 11 - 13, 2012
Bangalore IN
Read more... -
Equipment Calibration in FDA QSR – Regulations and Warning Letters
May 11, 2012
Palo Alto CA US
Read more... -
Logical Water System Validation
May 11, 2012
Palo Alto CA US
Read more... -
Pharmacokinetic - Pharmacodynamic data analysis
May 13 - 17, 2012
Cambridge BC UK
Read more... -
Pharmaceutical Networking Meeting PharmaVenue
May 14 - 15, 2012
Madrid ES
Read more... -
International Conference and Exhibition on Biosensors & Bioelectronics
May 14 - 16, 2012
Las Vegas NV US
Read more... -
The Drug Development Process - From Discovery to Commercialization
May 14 - 16, 2012
Los Angeles CA US
Read more... -
GMP Auditor Training (2 day)
May 14 - 15, 2012
Islington, London UK
Read more... -
PDA Chemistry Manufacturing & Controls (CMC) Workshop
May 14, 2012
Bethesda MD US
Read more... -
Medical Devices – EU Directives Guidance CE Marking and ISO Standard Certifications
May 14 - 15, 2012
Dublin IE
Read more... -
Auditing Clinical Trials for GCP Compliance
May 15 - 16, 2012
REGUS Boston Independence Wharf MA US
Read more... -
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
May 15 - 16, 2012
Los Angeles CA US
Read more... -
How to Survive the FDA Design Control Inspection: Common Problems and Risk mitigation
May 15, 2012
Palo Alto CA US
Read more... -
PDA/FDA Virus and TSE Safety Conference
May 15 - 17, 2012
Bethesda MD US
Read more... -
FDA Concerns on Alarm Standards and Safety
May 16, 2012
Palo Alto CA US
Read more... -
Practical Methods for Project Management
May 16 - 17, 2012
Dublin IE
Read more... -
Introduction to Good Manufacturing Practices
May 16 - 17, 2012
Regus Boston Independence Wharf, Boston, USA MA US
Read more... -
Best Practices for Maintaining an IND and IDE Application with FDA
May 16, 2012
Palo Alto CA US
Read more... -
ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
May 16 - 18, 2012
Los Angeles CA US
Read more... -
How to Audit API Manufacturers
May 16, 2012
Islington, London UK
Read more... -
Auditing and Qualifying Suppliers and Vendors - An Effective Risk Based Approach
May 17 - 18, 2012
Los Angeles CA US
Read more... -
Medical Devices – Developing Effective Post Market Surveillance and Complaint Handling Systems
May 17 - 18, 2012
Dublin IE
Read more... -
Analytical Test Methods Validation: FDA, ICH and USP Requirements
May 17, 2012
Palo Alto CA US
Read more... -
Advances in Raman spectroscopy in pharmaceutical analysis
May 17, 2012
London UK
Read more... -
An Introduction to Immunogenicity
May 17 - 18, 2012
REGUS Forrestal Village Princeton, NJ NJ US
Read more... -
HIPAA Privacy, Security and Breach Notification Compliance: Understanding the Requirements, Preventing Incidents, Surviving Audits, and Avoiding
May 17 - 18, 2012
Boston Marriott Long Wharf 8 AM to 5 PM EDT MA US
Read more... -
Oligonucleotide Therapeutics Discovery & Peptide Discovery and Development
May 20 - 23, 2012
Las Vegas MA US
Read more... -
TIDES: Oligonucleotides and Peptide Technology & Product Development & Applications of Nucleic Acids Technologies in Molecular Diagnostics
May 20 - 23, 2012
Las Vegas NV US
Read more... -
Writing Effective Standard Operating Procedures and Other Process Documents
May 21 - 22, 2012
Los Angeles CA US
Read more... -
Medical Devices – Field Actions and Their Management - Recalls, Product Recovery, Safety Alert
May 21 - 22, 2012
Dublin IE
Read more... -
FDA Inspections -What Regulators Expect and How to Prepare
May 21 - 22, 2012
Dublin IE
Read more... -
The EU Clinical Trial Directive
May 21 - 22, 2012
King of Prussia PA US
Read more... -
Pharma Outsourcing and Procurement Summit 2012
May 21 - 22, 2012
Berlin DE
Read more... -
Advances in Pharmaceutical Processing" (Complimentary Technical Seminar)
May 22, 2012
MONTREAL PQ CA
Read more... -
Comparability for Biologics
May 22 - 23, 2012
Prague CZ
Read more... -
EU Pharmaceutical Law Forum
May 22 - 23, 2012
Brussels BE
Read more... -
Supplier Controls to Meet Tougher U.S. FDA Requirements
May 22, 2012
Palo Alto CA US
Read more... -
Stability Testing in Pharmaceutical Development and Manufacturing (2 day)
May 22 - 23, 2012
London UK
Read more... -
Supplier Controls to Meet Tougher U.S. FDA Requirements
May 22, 2012
Palo Alto CA US
Read more... -
Biosimilars
May 22 - 23, 2012
Prague CZ
Read more... -
Effective Document Management for the Pharmaceutical, Biotech and Medical Device Industries
May 23 - 24, 2012
Los Angeles CA US
Read more... -
Bioavailability, Bioequivalence and Biowavers
May 23 - 24, 2012
Budapest HU
Read more... -
FDA Warning Letter - Consent Decree Software Validation
May 23, 2012
Palo Alto CA US
Read more... -
Outsourcing Pharmaceutical Manufacturing and Analytics
May 23 - 24, 2012
Hamburg DE
Read more... -
ADC Summit
May 23, 2012
London UK
Read more... -
Validation of Existing/ Legacy Computer Systems for FDA/EU Compliance
May 23, 2012
Palo Alto CA US
Read more... -
Pre-Approval Statements and Representations by Pharmaceutical Manufacturers
May 24, 2012
Palo Alto CA US
Read more... -
Advances in Pharmaceutical Processing
May 24, 2012
Research Triangle Park NC US
Read more... -
An Overview of Risk Management and Risk Analysis Techniques in Clinical Trials
May 24, 2012
Palo Alto CA US
Read more... -
Statistics for the Non-Statistician - US Seminar 2012 at Washington DC
May 24 - 25, 2012
Courtyard by Marriott Washington, DC ,8 AM to 5 P WA US
Read more... -
Non-Antibody Protein Production
May 24 - 25, 2012
Prague CZ
Read more... -
European Filing and Registration Procedures
May 28 - 29, 2012
Dublin IE
Read more... -
5th Annual Bio/Pharmaceutical Cold Chain Management Asia 2012
May 29 - 30, 2012
Singapore SG
Read more... -
European Lab Automation Congress and Exhibition
May 30 - 31, 2012
Hamburg DE
Read more... -
How do I Keep FDA Happy with my Contract Manufacturer
May 31, 2012
Palo Alto CA US
Read more... -
Risk-Based Validation Equipment Validation
May 31, 2012
Palo Alto CA US
Read more...
June 2012 [+] (48 total)
-
Device Corrections and Removals
June 1, 2012
Palo Alto CA US
Read more... -
Single Use Applications for Biopharmaceutical Manufacturing
June 4 - 6, 2012
San Francisco CA US
Read more... -
Good Clinical Practices (GCPs)
June 4 - 6, 2012
Los Angeles CA US
Read more... -
Practical Methods for Project Management
June 4 - 5, 2012
King of Prussia PA US
Read more... -
Comprehensive Overview of FDA Regulatory Compliance for Drug Products
June 4 - 5, 2012
Los Angeles PA US
Read more... -
Comprehensive Overview of FDA Regulatory Compliance for Drug Products
June 4 - 5, 2012
Los Angeles PA US
Read more... -
PDA/FDA Glass Quality Conference
June 4 - 5, 2012
Bethesda MD US
Read more... -
Vaccine Production Summit
June 4 - 6, 2012
San Francisco MA US
Read more... -
ICH Q10; moving from GMPs to a Pharmaceutical Quality System
June 5, 2012
Palo Alto CA US
Read more... -
Cell Line Development and Engineering
June 6 - 8, 2012
San Francisco MA US
Read more... -
Effective Internal and External Quality Assurance Auditing for FDA Regulated Industries
June 6 - 7, 2012
Los Angeles CA US
Read more... -
Latin America - Understanding Regulatory Compliance Requirements
June 6 - 8, 2012
Los Angeles CA US
Read more... -
Bio-IT World Asia 2012
June 6 - 8, 2012
Singapore SG
Read more... -
CLIA (Clinical Laboratory Improvement Amendments) Guidelines on Quality Control and Quality Assessment
June 7, 2012
Palo Alto CA US
Read more... -
Adverse Drug Events – Understanding and Reporting Requirements
June 7 - 8, 2012
Los Angeles CA US
Read more... -
The Electronic Common Technical Document (eCTD) - Building Comprehensive Functionality for Effective Implementation
June 11 - 12, 2012
King of Prussia PA US
Read more... -
Analytical Method Validation for Biologics, Biopharmaceuticals and Other Therapeutic Products
June 11 - 12, 2012
Los Angeles CA US
Read more... -
Pharmacokinetics in Drug Development - an Integrated Approach ( 2 day)
June 11 - 12, 2012
London UK
Read more... -
13th Drug Discovery Summit 2012
June 11 - 12, 2012
Zurich CH
Read more... -
Validation of Computer Systems
June 11 - 12, 2012
Los Angeles CA US
Read more... -
4th Annual Drug Development Summit 2012
June 11 - 12, 2012
Zurich UK
Read more... -
Global Pharma Manufacturing Summit 2012
June 11 - 12, 2012
New Jersey NJ US
Read more... -
FDA Inspections -What Regulators Expect and How to Prepare
June 12 - 13, 2012
Los Angeles CA US
Read more... -
FDA Warning Letter Closeout Program
June 12, 2012
Palo Alto CA US
Read more... -
QA/QC Strategy for Biopharmaceuticals and Biologics
June 13 - 15, 2012
Los Angeles CA US
Read more... -
How to Easily Copy, Migrate, and Archive Oracle Clinical Studies and Global Libraries
June 13, 2012
Virtual/Webinar/Webcast CA US
Read more... -
ADMET PK/TK and Drug Metabolism
June 14 - 15, 2012
Barcelona ES
Read more... -
2012 PDA Innovation and Best Practices on Sterile Technology Conference
June 18 - 19, 2012
Chicago IL US
Read more... -
Preparation of FDA Submissions (INDs, NDAs, BLAs, ANDAs, Post-Approval Supplements)and Communicating with the FDA
June 18 - 19, 2012
Los Angeles CA US
Read more... -
Reduce COTS Software Validation using the risk-based approach
June 19, 2012
Palo Alto CA US
Read more... -
Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
June 19 - 20, 2012
King of Prussia PA US
Read more... -
Cell-Based Assays
June 19 - 20, 2012
Berlin DE
Read more... -
Introduction to European Regulatory Affairs
June 19 - 21, 2012
REGUS Forrestal Village Princeton, NJ NJ US
Read more... -
CMC Regulatory Compliance for Biopharmaceuticals and Biologics
June 20 - 22, 2012
Los Angeles CA US
Read more... -
Genotoxic Impurities
June 20 - 21, 2012
Berlin DE
Read more... -
Process Validation
June 20 - 21, 2012
Berlin DE
Read more... -
Understanding and Implementing ISO 17025
June 20, 2012
Palo Alto CA US
Read more... -
Dissolution testing for the pharmaceutical industry
June 20 - 22, 2012
London UK
Read more... -
A basic introduction to the use and understanding of statistics in health and research
June 20 - 22, 2012
London UK
Read more... -
Acceptance Sampling by Variables Using Z1.9
June 22, 2012
Palo Alto CA US
Read more... -
Preparing the CMC Section for NDAs-CTDs-INDs
June 25 - 26, 2012
King of Prussia PA US
Read more... -
Lyophilization Technology - Practical Application of the Scientific Principles
June 25 - 27, 2012
Los Angeles CA US
Read more... -
Biosimilars – Understanding the Regulatory Challenges
June 25 - 26, 2012
Los Angeles CA US
Read more... -
Project Management for Phase 1 & 2 Clinical Trials
June 25 - 26, 2012
Los Angeles CA US
Read more... -
Next Generation Protein Therapeutics Summit
June 25 - 27, 2012
San Francisco CA US
Read more... -
CMC Analytical, Comparability and Stability Studies for Biotechnology Products
June 26 - 27, 2012
REGUS Forrestal Village Princeton, NJ NJ US
Read more... -
FDA's new enforcement initiative – Strategic Software Validation Planning for Executives and Managers
June 27, 2012
Palo Alto CA US
Read more... -
Project Management for Phase 3 and LCM (Life Cycle Management) of the Drug Development Process
June 27 - 28, 2012
Los Angeles CA US
Read more...
July 2012 [+] (20 total)
-
Social Mediai in the Pharmaceutical Industry
July 9 - 10, 2012
London UK
Read more... -
Biostatistics for Non-Statisticians
July 9 - 11, 2012
Los Angeles CA US
Read more... -
The European Chemicals Policy - REACH
July 9 - 10, 2012
REGUS Forrestal Village Princeton, NJ NJ US
Read more... -
Introduction to Effective Medical Writing
July 9 - 10, 2012
Los Angeles CA US
Read more... -
Verification of Compendial Methods According to the Revised USP Chapter <1226>
July 11, 2012
Palo Alto CA US
Read more... -
GAMP® 5 as applied to FDA software validation - strategies to avoid warning letters
July 11, 2012
Palo Alto CA US
Read more... -
Biobanking
July 11 - 12, 2012
London UK
Read more... -
Technical Writing for the Pharmaceutical, Medical Device, and Biotech Industries
July 11 - 13, 2012
Los Angeles CA US
Read more... -
Medical Devices – EU Directives Guidance CE Marking and ISO Standard Certifications
July 16 - 17, 2012
King of Prussia PA US
Read more... -
Pharmaceutical Production Batch Record Review
July 16 - 17, 2012
King of Prussia PA US
Read more... -
Aseptic Processing in the Manufacture of Biotech and Pharmaceutical Products
July 16 - 17, 2012
King of Prussia PA US
Read more... -
Project Management for Clinical Trials
July 18 - 19, 2012
Regus Boston Independence Wharf, Boston, USA MA US
Read more... -
Medical Devices – Developing Effective Post Market Surveillance and Complaint Handling Systems
July 19 - 20, 2012
King of Prussia PA US
Read more... -
Medical Devices – Field Actions and Their Management - Recalls, Product Recovery and Safety Alerts
July 23 - 24, 2012
King of Prussia PA US
Read more... -
European Filing and Registration Procedures
July 23 - 24, 2012
King of Prussia PA US
Read more... -
How to Monitor Pharmaceutical, Biologic and Medical Device Clinical Trials for GCP Compliance
July 23 - 24, 2012
Los Angeles CA US
Read more... -
Protein Expression Technologies from E. colit to Mammalian
July 23 - 25, 2012
King of Prussia PA US
Read more... -
Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
July 24 - 25, 2012
Los Angeles CA US
Read more... -
Comprehensive Overview of FDA Regulatory Compliance for Medical Devices
July 24 - 25, 2012
Los Angeles CA US
Read more... -
GCP Audits - Best Practices for Ensuring Compliance & Detecting Fraud and Misconduct in Clinical Trials
July 30 - 31, 2012
Los Angeles CA US
Read more...
August 2012 [+] (21 total)
-
Development and Validation of Bioanalytical Assays for Biologics: Quantification (PK) and Immunogenicity Assays
August 2 - 3, 2012
King of Prussia PA US
Read more... -
Clinical Biomarkers and Cancer
August 6 - 8, 2012
San Francisco MA US
Read more... -
Translating Biology to the Clinic
August 6 - 8, 2012
San Francisco MA US
Read more... -
Antibody Drug Development
August 6 - 8, 2012
San Francisco CA US
Read more... -
Active Pharmaceutical Ingredient (API) and Drug Product Specifications
August 6 - 8, 2012
Los Angeles CA US
Read more... -
Good Laboratory Practices for Pre-Clinical Testing
August 6 - 7, 2012
Los Angeles CA US
Read more... -
Diagnostic Development
August 6 - 8, 2012
San Francisco CA US
Read more... -
Good Manufacturing Practices
August 8 - 10, 2012
Los Angeles CA US
Read more... -
Spreadsheet Validation: Understanding and satisfying FDA requirements
August 8, 2012
Palo Alto CA US
Read more... -
Stability Programs for Product Shelf Life - From Development to Approval
August 9 - 10, 2012
Los Angeles CA US
Read more... -
The Drug Development Process - From Discovery to Commercialization
August 15 - 17, 2012
King of Prussia PA US
Read more... -
2nd World Congress on Vaccines & Vaccination
August 20 - 22, 2012
Chicago IL US
Read more... -
Vendor Oversight
August 21 - 22, 2012
San Francisco CA US
Read more... -
SUBJECT: THE 12TH INTERNATIONAL MEDICAL, HOSPITAL & PHARMACEUTICAL EXHIBITION IN VIETNAM
August 22 - 25, 2012
Ho Chi Minh VN
Read more... -
Mastering your Performance as a QA Professional
August 22 - 23, 2012
San Francisco CA US
Read more... -
The 6 Most Common Problems in FDA Software Validation & Verification
August 22, 2012
Palo Alto CA US
Read more... -
THE 12TH INTERNATIONAL MEDICAL, HOSPITAL & PHARMACEUTICAL EXHIBITION ON AUGUST 22TH-25TH, 2012
August 22 - 25, 2012
Ho Chi Minh City VN
Read more... -
Writing Standard Operating Procedures
August 23 - 24, 2012
REGUS, SOMA, San Francisco CA US
Read more... -
International Conference on Occupational Health & Safety Summit-2012
August 27 - 29, 2012
Chicago IL US
Read more... -
cGMP Quality Principles for Pharmaceuticals, Biopharmaceuticals, Biologics and Medical Devices
August 27 - 29, 2012
Los Angeles CA US
Read more... -
Pharmaceutical, Biopharmaceutical, and Biologics Quality Control Laboratories: A Regulatory Compliance Primer
August 30 - 31, 2012
Los Angeles CA US
Read more...
September 2012 [+] (34 total)
-
Introduction to Molecular Biology Techniques
September 5 - 7, 2012
King of Prussia PA US
Read more... -
Validation and use of Excel spreadsheets in FDA regulated environments
September 5, 2012
Palo Alto CA US
Read more... -
Validation of Computer Systems
September 6 - 7, 2012
King of Prussia PA US
Read more... -
The Royal Pharmaceutical Society Annual Conference 2012
September 9 - 10, 2012
Birmingham UK
Read more... -
Royal Pharmaceutical Society Awards 2012
September 9, 2012
Birmingham UK
Read more... -
Design Control for Medical Device Professionals
September 10 - 11, 2012
Berlin DE
Read more... -
Biopharma Asia Congress 2012
September 10 - 11, 2012
Singapore SG
Read more... -
Clinical Document Management - A Trial by Trial Approach to Compliance
September 10 - 11, 2012
King of Prussia PA US
Read more... -
Cell Therapy Bioprocessing
September 10 - 11, 2012
National Harbor MD US
Read more... -
How to Implement Risk Management Principles and Activities Within A Quality Management System
September 10 - 11, 2012
King of Prussia PA US
Read more... -
World Congress and Expo on Biowaivers and Biosimilars
September 10 - 12, 2012
San Antonio TX US
Read more... -
2012 PDA/FDA Joint Regulatory Conference
September 10 - 12, 2012
Baltimore MD US
Read more... -
Pharma CI Conference & Exhibition
September 11 - 12, 2012
Parsippany NJ US
Read more... -
ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
September 12 - 14, 2012
King of Prussia PA US
Read more... -
Process Validation for Medical Devices
September 12 - 14, 2012
King of Prussia PA US
Read more... -
2012 PDA ICH Q10 Workshop: Expectations of Operations & Executive Management
September 12 - 13, 2012
Baltimore MD US
Read more... -
Selecting and Managing CROs
September 12 - 13, 2012
King of Prussia PA US
Read more... -
Design Validation, Verification, and Risk Analysis for Medical Device Professionals
September 12 - 13, 2012
Berlin DE
Read more... -
The EU Clinical Trial Directive
September 17 - 18, 2012
Dublin IE
Read more... -
10th Annual Pharmaceutical IT Congress
September 17 - 18, 2012
London UK
Read more... -
ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
September 17 - 19, 2012
Dublin IE
Read more... -
ADME, PK/TK, and Drug Metabolism in Drug Discovery and Development
September 17 - 19, 2012
Dublin IE
Read more... -
International Conference on Obesity and Weight Management
September 17 - 19, 2012
San Antonio TX US
Read more... -
Introduction to Medical Combination Products
September 18 - 19, 2012
King of Prussia PA US
Read more... -
Best Practices For An Effective Cleaning Validation Program
September 18 - 19, 2012
King of Prussia PA US
Read more... -
Risk Assessment-Compliance Using Easy To Fill Out Documentation
September 18, 2012
Palo Alto CA US
Read more... -
3rd Annual Pharmacovigilance Asia 2012
September 19 - 20, 2012
Singapore SG
Read more... -
Auditing Clinical Trials for GCP Compliance
September 19 - 20, 2012
Princeton NJ US
Read more... -
Introduction to Good Manufacturing Practices
September 20 - 21, 2012
Regus Princeton - Forrestal Village, New Jersey, U NJ US
Read more... -
Introduction to Medical Device Submissions - 510ks, PMAs, and Exemptions
September 20 - 21, 2012
King of Prussia PA US
Read more... -
Process Validation for Drugs and Biologics
September 20 - 21, 2012
King of Prussia PA US
Read more... -
International Conference & Exhibition on Food Processing and Technology
September 24 - 26, 2012
Hyderabad IN
Read more... -
AlgeriaPharma 2012
September 25 - 27, 2012
Algiers DZ
Read more... -
CMC Analytical, Comparability and Stability Studies for Biotechnology Products
September 26 - 27, 2012
REGUS Boston Independence Wharf MA US
Read more...
October 2012 [+] (14 total)
-
Rhode Island Convention Center
October 7 - 12, 2012
Providence RI US
Read more... -
PDA Biennial Training Conference
October 8 - 9, 2012
Bethesda MD US
Read more... -
Formulation Strategies for Protein Therapeutics
October 9 - 11, 2012
Providence RI US
Read more... -
2nd Annual Oncology Biomarkers Congress
October 10 - 11, 2012
Manchester UK
Read more... -
Oncology Clinical Development Congress
October 10 - 11, 2012
Manchester UK
Read more... -
The Universe of Pre-filled Syringes & Injection Devices
October 15 - 17, 2012
Las Vegas NV US
Read more... -
Introduction to European Regulatory Affairs
October 17 - 19, 2012
REGUS Boston Prudential Tower MA US
Read more... -
An Introduction to Immunogenicity
October 17 - 18, 2012
REGUS, SOMA, San Francisco CA US
Read more... -
International Conference on Clinical and Cellular Immunology
October 22 - 24, 2012
chicago noth shore IL US
Read more... -
PDA’s 7th Annual Global Conference on Pharmaceutical Microbiology
October 22 - 24, 2012
Bethesda MD US
Read more... -
The European Chemicals Policy - REACH
October 29 - 30, 2012
REGUS Mission Valley, San Diego CA US
Read more... -
Indian Lab Automation Conference and Exhibition
October 30 - 31, 2012
Mumbai IN
Read more... -
Well Characterized Biologicals
October 30, 2012 - November 1, 2012
Washington DC US
Read more... -
Process 2 Product
October 31, 2012 - November 1, 2012
Washington DC US
Read more...
November 2012 [+] (11 total)
-
2nd World Congress on Cell Science & Stem Cell Research
November 12 - 14, 2012
San Antonio TX US
Read more... -
PDA/FDA Pharmaceutical Supply Chain Conference
November 13 - 14, 2012
Bethesda MD US
Read more... -
2012 Pharmaceutical Cold Chain & Good Distribution Practice Conference
November 15 - 16, 2012
Bethesda MD US
Read more... -
Global Biofuels & Bioproducts Summit
November 19 - 21, 2012
Antonio TX US
Read more... -
International Conference and Exhibition on Probiotics-2012
November 19 - 21, 2012
San Antonio TX US
Read more... -
2nd World Congress on Pharmaceutical Regulatory Affairs
November 23 - 24, 2012
HYDERABAD CT IN
Read more... -
International Conference on Hair Transplantation & Trichology 2012
November 26 - 28, 2012
San Antonio TX US
Read more... -
International Conference on Hair Transplantation & Trichology 2012
November 26 - 28, 2012
San Antonio TX US
Read more... -
International Conference and Exhibition on Surgery & Transplantation
November 26 - 28, 2012
San Antonio TX US
Read more... -
HPLC Analytical Method Development and Validation (2 day)
November 27 - 28, 2012
London UK
Read more... -
Project Management for Clinical Trials
November 29 - 30, 2012
REGUS Mission Valley, San Diego CA US
Read more...
December 2012 [+] (4 total)
-
Antibody Engineering & Antibody Therapeutics
December 2 - 6, 2012
San Diego CA US
Read more... -
PDA/FDA Vaccines Conference
December 3 - 4, 2012
Bethesda MD US
Read more... -
Writing Standard Operating Procedures
December 3 - 4, 2012
REGUS, SOMA, San Francisco CA US
Read more... -
Vendor Oversight
December 6 - 7, 2012
San Francisco CA US
Read more...
Post Your Event
FREE Listing
Click here to submit information and post your event on this site for free.