Webcasts - Pharmaceutical Technology

Latest Issue
PharmTech

Latest Issue
PharmTech Europe
   Printer friendly page
Webcasts

WEBCASTS

LIVE WEBCASTS

 

Trends in Safe Handling of Potent Compounds in Pharmaceutical Manufacturing Processes
May 15, 2013 at 11:00 AM EDT

What does “highly potent” mean and what is required to manufacture these drugs from an equipment containment perspective? This 60-minute webcast will focus on the safe handling of high potent drugs and meeting the GMP requirements for minimizing cross-contamination to other drugs manufactured in the same facility. The use of control banding will also be discussed.

Register Free at http://www.pharmtech.com/trends

Sponsor:
Patheon

 

Minimizing Out-of-Specification (OOS) Errors Using a Risk-based Gravimetric Approach
Wednesday, May 22, 2013 at 11:00 AM EDT

Experts, including Dr. Charles Ray, former Associate Director of Analytical R&D at Bristol-Myers Squibb, describe why out-of-specification (OOS) results are a problem in analytical workflows and demonstrate how to improve the efficiency and variability of sample preparation. Find out how to identify and address the potential sources of error in weighing and sample-preparation processes that cause OOS results.

Register Free at http://www.pharmtech.com/minimizingOOS

Sponsor:
Mettler Toledo

 

Risk Mitigation for Alcohol-Dose Dumping in Controlled Release Forms
Thursday, May 23, 2013 at 10:00 AM EDT

Learn more from industry and regulatory experts about the regulatory and technical considerations in implementing QbD in controlled release formulations. Learn how to design controlled release formulations solutions that remain robust in the presence of alcohol and of the critical material, formulation and performance attributes of alcohol-resistant coatings

Register Free at http://www.pharmtech.com/alcohol

Sponsor:
FMC

 

Cleaning Validation: Science, Risk, and Novel Approaches to Testing
Tuesday, June 4, 2013 at 11:00 AM EDT

Pharmaceutical cleaning validation programs can consume tremendous resources unless a structured approach is considered.  This webcast will convey the current science-driven risk-based approach to cleaning validation as well as the use of LC/MS methods for rapid development and testing of cleaning samples.

Register Free at http://www.pharmtech.com/testing

Sponsor:
Patheon


ARCHIVED WEBCASTS

New Strategies for Evaluating BioPharmaceutical Stability
Sponsored by: ABC Labs
Sign Up Now>>

Available through May 9, 2014

A Pragmatic Application of QbD: Turning Theory into Tangible Success
Sponsored by: Patheon
Sign Up Now>>

Available through May 2, 2014

USP Outlook: Key Program Activity for 2013
Sponsored by:USP
Sign Up Now>>

Available through April 16, 2014

Optimizing Validation/Mapping Studies for GMP Compliance
Sponsored by: Vaisala
Sign Up Now>>

Available through April 10, 2014

A Quality by Design Approach for Stability Testing
Sponsored by: Decagon
Sign Up Now>>

Available through March 26, 2014

Optimizing Quality by Design in Bulk Powders and Solid Dosage
Sponsored by: Hovione
Sign Up Now>>

Available through March 21, 2014

Accelerate Sterile and Non-Sterile Clinical Trial Manufacturing with Single-Use Technologies
Sponsored by: Patheon
Sign Up Now>>

Available through March 6, 2014

Improving Cell Culture Productivity: Best Practices for Automation and Control
Sponsored by Parker Hannifin
Sign Up Now>>

Available through January 29, 2014

Overcoming Formulation Challenges of Parenteral Drugs
Sponsored by Croda
Sign Up Now>>

Available through December 11, 2013

Best Practices for Achieving Product Quality in Sterile Manufacturing
Sponsored by Baxter
Sign Up Now>>

Available through December 10, 2013

Accelerate the Development of Challenging Drug Candidates via Crystal Engineering
Sponsored by Catalent
Sign Up Now>>

Available through December 6, 2013

Application of QWBA and Short Lived Isotopes in the Drug Development Paradigm
Sponsored by MPI Research
Sign Up Now>>

Available through November 11, 2013

API Development: Risk and Control of Genotoxic Impurities
Sponsored by Neuland
Sign Up Now>>

Available through November 8, 2013

Achieving Sensory Benefits and Mildness in Dermatology Products
Sponsored by BASF
Sign Up Now>>

Available through October 4, 2013

Overcoming Challenges with Pediatric Oral Solid Dose Development
Sponsored by Colorcon
Sign Up Now>>

Available through October 3, 2013

Increasing Your Chances for Success in First-Man Studies
Sponsored by Patheon
Sign Up Now>>

Available through October 3, 2013

Risk Management in Sterile Manufacturing
Sponsored by DPT
Sign Up Now>>

Available through September 27, 2013

Osmotic Controlled Release Oral Delivery System
Sponsored by Patheon
Sign Up Now>>

Available through September 19, 2013

Recent USP Changes - Regulatory and Quality Aspects of Sample Preparation
Sponsored by Mettler Toledo
Sign Up Now>>

Available through September 18, 2013

Omega-3 Innovations in Pharmaceutical and Diagnostic Markets
Sponsored by Catalent
Sign Up Now>>

Available through September 10, 2013

Atypical Visible Particles (Black Specks): Approaches for Manufacturers and Users
Sponsored by IPEC
Sign Up Now>>
Available through September 10, 2013

Path to Zero Landfill: Learn how One Company is Leading the Way
Sponsored by Kimberly Clark
Sign Up Now>>
Available through August 21, 2013

Unlocking the Power of New Softgel Technology for Multiple API Formulations
Sponsored by Patheon
Sign Up Now>>
Available through July 26, 2013

Bioavailability Enhancement Using Lipid-Based Drug Delivery
Sponsored by Catalent
Sign Up Now>>
Available through June 20, 2013

Screening Methods for Elemental Impurities: Proposed Compendial Requirements
Sponsored by SGS Life Science Services
Sign Up Now>>
Available through June 14, 2013

Applying Quality by Design in Tablet Coatings
Sponsored by ColorCon
Sign Up Now>>
Available through June 13, 2013

When Softgels Are a Good First Option: Overcoming Bioavailability Challenges
Sponsored by Patheon
Sign Up Now>>
Available through June 12, 2013

For questions contact Sara Barschdorf

ADVERTISEMENT

LCGC E-mail Newsletters

Subscribe: Click to learn more about the newsletter
| Weekly
| Monthly
|Monthly
| Weekly

Survey
How does your company apply quality-by-design (QbD) principles to manufacturing processes?
To all processes for both new and legacy products
To all process for new products only
To select process for new products only
To select processes for both new and legacy products
Do not use QbD
To all processes for both new and legacy products
21%
To all process for new products only
13%
To select process for new products only
26%
To select processes for both new and legacy products
21%
Do not use QbD
21%
View Results
Eric Langer Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
Patricia Van Arnum Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
Nathan Jessop Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
Lynn Torbeck Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality
 More
FindPharma Custom Search
Featured Jobs

More Jobs
Click here