|
HOW TO PREPARE A RISK ASSESSMENT FOR CROSS CONTAMINATION
August 19 , 2010 - View Details
QbD: HOW TO FIT THE BUILDING BLOCKS TOGETHER
August 17 , 2010 - View Details
Evaluating Contamination Concerns forAseptic Manufacturing and Sterility Testing Isolators
June 29 , 2010 - View Details
Validation of Water Systems in the Biopharmaceutical Industry
June 27 , 2010 - View Details
FLEXIBLE CONTAINMENT OF POTENT COMPOUNDS
June 22 , 2010 - View Details
Validation and Change Control: The Validation Life Cycle
June 20 , 2010 - View Details
Filter Dryers In Technology Transfer and Scale-up
June 14 , 2010 - View Details
PROCESS VALIDATION
June 13 , 2010 - View Details
Troubleshooting Microbial Excursions
June 28 , 2010 - View Details
Investigating Deviations and Failures in The Pharmaceutical Industry
June 24 , 2010 - View Details
Hydrogen Peroxide Vapor Decontamination for the Highest Level of Microbial Control in a Pharmaceutical Facility
June 17 , 2010 - View Details
Cleaning Validation
June 15 , 2010 - View Details
VALIDATION AND PERFORMANCE TESTING OF ANTIMICROBIAL TECHNOLOGIES
June 8 , 2010 - View Details
21 CFR Part 11 Compliance How to Save Money with Electronic Signatures and Records Compliance
June 3 , 2010 - View Details
RELATIVE HUMIDITY MEASUREMENT IN REGULATED AND CRITICAL ENVIRONMENTS
May 26, 2010 - View Details
Designing and Implementing an Effective Cleaning and Disinfection Program
May 21, 2010 - View Details
Risk-Based Approach to Computer & Software Validation
May 19, 2010 - View Details
Validation of Heating Ventilation and Air Conditioning Systems
May 18, 2010 - View Details
CONTAINMENT OF PHARMACEUTICAL POWDERS
May 12, 2010 - View Details
HEALTH-BASED RISK ASSESSMENTS FOR POTENT COMPOUNDS
May 11, 2010 - View Details
Designing and Implementing an Effective Cleaning and Disinfection Program
May 7, 2010 - View Details
HOW TO PREPARE A RISK ASSESSMENT FOR CROSS CONTAMINATION
May 5, 20100 - View Details
Designing and Implementing an Effective Cleaning and Disinfection Program
May 4, 2010 - View Details
FLEXIBLE CONTAINMENT OF POTENT COMPOUNDS
April 16, 2010 - View Details
PROCESS VALIDATION
April 13, 2010 - View Details
RETROFIT FOR CONTAINMENT OF POTENT COMPOUNDS
April 8, 2010 - View Details
Thermal Validation
March 31, 2010 - View Details
Cleaning Validation
March 30, 2010 - View Details
Troubleshooting Microbial Excursions
March 26, 2010 - View Details
UNDERSTANDING Human Machine Interface: High-Performance HMI
March 24, 2010 - View Details
Disinfectant Validation
March 18, 2010 - View Details
FDA Inspections: What to expect And How to prepare (Part I and II)
March 2nd and 3rd, 2010 - View Details
Investigating Deviations and Failures in The Pharmaceutical Industry
February 23 , 2010 - View Details
Contamination Control in Pharmaceutical, Biotech, and Medical Device Clean rooms
February 22 , 2010 - View Details
Designing and Implementing an Effective Cleaning and Disinfection Program
February 19 , 2010 - View Details
High Containment Applications for Large Scale Formulation Production
February 18 , 2010 - View Details
ALARM MANAGEMENT It's a Process, Not a Product
February 17 , 2010 - View Details
Outsourcing in the Healthcare Industry How to Avoid the Perils and Pitfalls
February 16 , 2010 - View Details
Validation and Change Control: The Validation Life Cycle
February 9 , 2010 - View Details
Troubleshooting Microbial Excursions
January 26 , 2010 - View Details
Risk Assessment Strategies to Lower Cost of Goods
January 25 , 2010 - View Details
RETROFIT FOR CONTAINMENT OF POTENT COMPOUNDS
January 22 , 2010 - View Details
HOW TO PREPARE A RISK ASSESSMENT FOR CROSS CONTAMINATION
January 21 , 2010 - View Details
FLEXIBLE CONTAINMENT OF POTENT COMPOUNDS
January 20 , 2010 - View Details
PROCESS VALIDATION Process Design, Process Qualification, Continuous Process Verification
January 19 , 2010 - View Details
FDA Inspections: What to expect And How to prepare (PARTS 1 and 2)
December 21 and 22 , 2009 - View Details
21 CFR Part 11 Compliance and Validation for Databases and Spreadsheets
December 17 , 2009 - View Details
CLEANING EXTERNAL SURFACES FOR COMPLIANCE IN SHARED FACILITIES
December 16 , 2009 - View Details
DEVELOPING, IMPLEMENTING or UPGRADING FOR AN EFFECTIVE PROCESS MANAGEMENT SYSTEM
December 15 , 2009 - View Details
RETROFIT FOR CONTAINMENT OF POTENT COMPOUNDS
December 9 , 2009 - View Details
VALIDATION AND PERFORMANCE TESTING OF ANTIMICROBIAL TECHNOLOGIES
December 8 , 2009 - View Details
CONTAINMENT OF PHARMACEUTICAL POWDERS
November 23 , 2009 - View Details
HOW TO AVOID 483’s AND SAVE MONEY IN MULTIPRODUCT FACILITIES
November 20 , 2009 - View Details
Designing and Implementing an Effective Cleaning and Disinfection Program
November 19 , 2009 - View Details
ALARM MANAGEMENT
It's a Process, Not a Product
November 17 , 2009 - View Details
Validation and Change Control: The Validation Life Cycle
November 16 , 2009 - View Details
FLEXIBLE CONTAINMENT OF POTENT COMPOUNDS
October 28 , 2009 - View Details
HOW TO PREPARE A RISK ASSESSMENT FOR CROSS CONTAMINATION
October 27 , 2009 - View Details
Environmental Monitoring
October 20 , 2009 - View Details
STRATEGIES FOR REDUCING PROCESS RISK
October 19 , 2009 - View Details
ASTM E2500 CONSENSUS STANDARD
October 6 , 2009 - View Details
PROCESS VALIDATION
Process Design, Process Qualification, Continuous Process Verification
September 29 , 2009 -
View Details
RETROFIT FOR CONTAINMENT OF POTENT COMPOUNDS
September 24 , 2009 -
View Details
QbD: HOW TO FIT THE BUILDING BLOCKS TOGETHER
September 23 , 2009 -
View Details
RISK-BASED APPROACH TO GMP COMPLIANCE
Understanding FDA and ICH Guidances and the ASTM Standard approach to Risk based GMP compliance.
September 22 , 2009 -
View Details
VALIDATION AND PERFORMANCE TESTING OF ANTIMICROBIAL TECHNOLOGIES
September 18 , 2009 -
View Details
HOW PROCESS AND PROCESS EQUIPMENT CAN IMPROVE REGULATORY AND SAFETY CONSIDERATIONS
September 17 , 2009 -
View Details
HOW TO PREPARE A RISK ASSESSMENT FOR CROSS CONTAMINATION
September 16 , 2009 -
View Details
Understanding FDA and ICH Guidance, and ASTM Standard approach to Risk based GMP compliance
August 25, 2009 -
View Details
Designing and Implementing an Effective Cleaning and Disinfection Program
August 27, 2009 -
View Details
RETROFIT FOR CONTAINMENT OF POTENT COMPOUNDS
August 26, 2009 -
View Details
HOW PROCESS AND PROCESS EQUIPMENT CAN IMPROVE REGULATORY AND SAFETY CONSIDERATIONS
August 19, 2009 -
View Details
Designing and Implementing an Effective Cleaning and Disinfection Program
August 18, 2009 -
View Details
QbD: HOW TO FIT THE BUILDING BLOCKS TOGETHER
August 17, 2009 -
View Details
HOW TO CONTROL CROSS CONTAMINATION AND SAVE MONEY THROUGH ROOM AND AIRLOCK DESIGN
July 27, 2009 -
View Details
RETROFIT FOR CONTAINMENT OF POTENT COMPOUNDS
July 28, 2009 -
View Details
HOW TO PREPARE A RISK ASSESSMENT FOR CROSS CONTAMINATION
July 21, 2009 -
View Details
HOW TO MAXIMIZE PROCESSING SPACE WHILE PROTECTING AGAINST CROSS CONTAMINATION IN MULTI-PRODUCT FACILITIES
July 1, 2009 -
View Details
UNDERSTANDING REGULATORY AND MATERIAL REQUIREMENTS WHEN PROCESSING WITH FLEXIBLE CONTAINMENT
June 30, 2009 -
View Details
HOW TO SAVE MONEY AND INCREASE SAFETY WITH FLEXIBLE CONTAINMENT
June 25, 2009 -
View Details
VALIDATION AND PERFORMANCE TESTING OF ANTIMICROBIAL TECHNOLOGIES
June 19, 2009 -
View Details
FLEXIBLE VERSUS RIGID CONTAINMENT OF POTENT COMPOUNDS
May 27, 2009 -
View Details
OEL IMPLEMENTATION
May 28, 2009 -
View Details
HOW TO PREPARE A RISK ASSESSMENT FOR CROSS CONTAMINATION
May 28, 2009 -
View Details
UNDERSTANDING REGULATORY AND MATERIAL REQUIREMENTS WHEN PROCESSING WITH FLEXIBLE CONTAINMENT
May 21, 2009 - View Details
Designing and Implementing an Effective Cleaning and Disinfection Program
May 20, 2009 - View Details
HOW TO IMPLEMENT CONTAINMENT UPGRADES (IBCs AND IN-LINE PROCESSING) TO A PHARMACEUTICAL R&D SOLIDS DEVELOPMENT SUITE
April 29, 2009 - View Details
HOW TO PREPARE A RISK ASSESSMENT FOR CROSS CONTAMINATION
April 28, 2009 - View Details
RETROFIT FOR CONTAINMENT OF POTENT COMPOUNDS
April 22, 2009 - View Details
FLEXIBLE ENCLOSURES FOR HANDLING POTENT COMPOUNDS
April 21, 2009 - View Details
HOW TO BEST PREPARE, PROTECT AND CLEAN EXTERNAL SURFACES
April 2, 2009 - View Details
HOW TO CLEAN EXTERNAL SURFACES
February 29 , 2009 - View Details
|
