Pharmaceutical Events. (Posted: July 2010)| PharmiWeb.com
Pharmaceutical Events - PharmiWeb.com
Upcoming events in the Pharmaceutical Industry.
Health-Related Quality Of Life Research – FDA and Pros: What to Do In 2010 and Beyond?
From 23 July 2010 to 23 July 2010
Learn about HRQOL, the concept, strategies, process and how to interpret HRQOL results accurately.
Venue: Online Event
the 2nd International Forum on Pandemic Influenza
From 24 July 2010 to 25 July 2010
Venue: Qingdao, China
Workshop on Managing Pharmaceutical Water Systems
From 26 July 2010 to 27 July 2010
Workshop on Managing Pharmaceutical Water Systems
Venue: Holiday Inn Atrium, Singapore
BioProcess Asia Pacific
From 26 July 2010 to 28 July 2010
Understand the strategies to create flexible facility & forecast future requirements
Venue: Singapore
Cleanroom Microbiology for the Non-Microbiologist
From 27 July 2010 to 28 July 2010
Venue: Costa Mesa, CA
Product Risk Management - ISO 14971 and ICH Q9
From 27 July 2010 to 27 July 2010
In this Product Risk Management webinar learn how to develop and implement product risk management planning. Understand the Key requirements of ISO 14971 and ICH Q9.
Venue: Online Event
Antibody Engineering & Design
From 27 July 2010 to 29 July 2010
Venue: Boston
Sterilization Procedures: Technology, Equipment & Validation
From 29 July 2010 to 30 July 2010
Venue: Costa Mesa, CA
Project Management and Change Control - Get It Right The First Time
From 29 July 2010 to 30 July 2010
Project Management and Change Control
Venue: Harris Hotel Tebet, Jakarta, Indonesia
Drug Master Files (DMF's)
From 29 July 2010 to 29 July 2010
In this Drug Master Files (DMF's) training learn how and why the DMF's is submitted to FDA and how it intended to be used.
Venue: Online Event
Troubleshooting ethylene oxide (EO) processes
From 29 July 2010 to 29 July 2010
This EO sterilization training Webinar will discuss the important parameters to measure for the sterility assurance level and actions to take if they are not compliant to the process specification.
Venue: Online Event
WORKING THROUGH DRUG DEVELOPMENT
From 29 July 2010 to 30 July 2010
MANAGEMENT FORUM'S SUMMER SCHOOL
Venue: The Rembrandt Hotel, London
BIT's 1st World Congress of Virus and Infections-2010
From 31 July 2010 to 03 August 2010
Voice of Virologists
Venue: BEXCO, Busan, South Korea
Leadership Experience
From 02 August 2010 to 12 August 2010
Venue: Boston, MA USA
International Intellectual Property Law Summer School
From 02 August 2010 to 05 August 2010
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
Venue: Cambridge
Selecting and Managing CRO's
From 03 August 2010 to 04 August 2010
Venue: Costa Mesa, CA
Drug Master Files (DMFs) - Understanding and Meeting Your Regulatory and Processing Responsibilities
From 05 August 2010 to 06 August 2010
Venue: Costa Mesa, CA
Medical Management in Medicare Advantage: A Payer/Provider Collaborative Care Summit
From 05 August 2010 to 06 August 2010
Venue: Loews Coronado Bay
Medical Management in Medicare Advantage:Payer/Provider Collaborative Care Summit
From 05 August 2010 to 06 August 2010
Venue: Loews Coronado Bay Resort
Pharmaceutical Quality Forum: CMC Compliance
From 07 August 2010 to 08 August 2010
Venue: Ahmedabad, India
Latin America - Understanding Regulatory Compliance Requirements
From 09 August 2010 to 10 August 2010
Venue: Costa Mesa, CA
How to Develop an Effective Complaint Handling, and Post Market Surveillance Program
From 09 August 2010 to 10 August 2010
Venue: Costa Mesa, CA
Cost Contained Regulatory Compliance for the Drug, Biologics and Medical Device Industries
From 09 August 2010 to 11 August 2010
Venue: Costa Mesa, CA
Regulatory Affairs Part I: The IND Phase and Part II: The NDA Phase
From 09 August 2010 to 13 August 2010
Venue: Boston, MA USA
European Regulatory Affairs
From 09 August 2010 to 10 August 2010
Venue: Horsham, PA USA
PHARMACOKINETICS: Essential Theory and Practical Considerations
From 09 August 2010 to 11 August 2010
Venue: Acadia University, Wolfville, Nova Scotia, Canada
Auditing and Qualifying API Suppliers
From 10 August 2010 to 11 August 2010
Venue: Washington
Root Cause Analysis for CAPA
From 11 August 2010 to 13 August 2010
Venue: Costa Mesa, CA
Streamline Documentation System in Pharmaceutical Laboratory
From 11 August 2010 to 11 August 2010
This laboratory documentation training Webinar will discuss the GMP requirements on laboratory records and how to streamline documentation system.
Venue: Online Event
Japan - Regulatory Filing Requirements and Compliance Processes for Life Sciences
From 11 August 2010 to 12 August 2010
Venue: Costa Mesa, CA
FDA Inspections - What to Expect and How to Prepare
From 16 August 2010 to 17 August 2010
Venue: Costa Mesa, CA
Adverse Drug Events – Reporting & Regulatory Requirements
From 16 August 2010 to 17 August 2010
Venue: Costa Mesa, CA
Writing Effective Standard Operating Procedures and Other Process Documents
From 16 August 2010 to 17 August 2010
Venue: King of Prussia, PA, USA
The International API GMP Guidance: ICH Q7 Implementation and Application
From 17 August 2010 to 18 August 2010
Venue: Montreal Airport
Process Validation Workshops for pharmaceutical
From 17 August 2010 to 18 August 2010
Venue: Montreal Airport
The Drug Development Process - From Discovery to Commercialization
From 18 August 2010 to 20 August 2010
Venue: Costa Mesa, CA
Comprehensive Overview of FDA Regulatory Compliance for Drugs and Biotech Products
From 18 August 2010 to 19 August 2010
Venue: Costa Mesa, CA
NDDS India 2010: Novel Drug Delivery Systems
From 19 August 2010 to 20 August 2010
Leveraging technological advances in novel drug delivery systems
Venue: The Westin Mumbai Garden City, Mumbai, India
Writing in the Regulated Environment When English Is Your Second Language
From 19 August 2010 to 20 August 2010
Venue: King of Prussia, PA, USA