Webcasts - Pharmaceutical Technology

Webcasts

WEBCASTS

LIVE WEBCASTS

Regulatory, Biosafety, and Clinical Considerations for Vaccine Development
Tuesday, June 11, 2013 at 11:00 AM EDT for the US and Tuesday, June 18, 2013 at 3:00 PM CET for Europe

The development and approval processes for a vaccine requires understanding of regulatory, biosafety, and clinical issues. This webcast provides a global perspective of these key issues, plus a detailed a case study examining viral challenge testing for vaccine development in a phase I clinical pharmacology unit.

Sponsor:
SGS Life Science Services

Ensuring Global Regulatory Compliance for Product Registrations: Strategies for Risk Reduction and Operational Efficiency
Tuesday, June 11, 2013 at 2:00 PM EDT

Learn from industry and regulatory experts on how to create a robust quality management system for complying with country-based and regional-based regulatory requirements for product registration, product changes, and labeling changes. Gain insight into how to use automation for effectively tracking product registration and related correspondence to ensure global regulatory compliance.

Sponsor:
Sparta Systems

Achieving Raw-Material Transparency in the Pharmaceutical/ Biopharmaceutical Supply Chain
Tuesday, June 18, 2013 at 11:00 AM EDT

Understand how to apply quality risk management in the biopharmaceutical/ pharmaceutical supply chain. Learn how to resolve operational challenges and the steps required to balance cost and availability while minimizing risk to secure a quality supply chain for raw materials for use in biopharmaceuticals.

Sponsor:
SAFC

Risk-Mitigation Strategies for API Manufacturing in Emerging Markets
Wednesday, June 19, 2013 at 11:00 AM EDT

Understand how to align your company’s strategy with external manufacturing partners to facilitate access to local markets, manage complex supply chains, meet global and national regulatory standards and secure production of APIs and Intermediates. Learn from pharmaceutical companies and industry experts on risk-mitigation strategies in supplier selection and qualification in emerging markets.

Sponsor:
Neuland

Overcoming Challenges in Development of Oral Enteric and Controlled-Release Dosage Forms
Thursday, July 18, 2013 at 11:00 AM EDT

Developing the right release profile - Three industry experts discuss challenges of developing enteric and controlled-release properties in a variety of solid dosage forms such as multi-particulate, tablets, capsules and softgels.

Sponsor:
Patheon

ARCHIVED WEBCASTS

Cleaning Validation: Science, Risk, and Novel Approaches to Testing
Sponsored by: Patheon
Sign Up Now>>

Available through June 4, 2014

Risk Mitigation for Alcohol-Dose Dumping in Controlled Release Forms
Sponsored by: FMC
Sign Up Now>>

Available through May 23, 2014

Minimizing Out-of-Specification (OOS) Errors Using a Risk-based Gravimetric Approach
Sponsored by: Mettler Toledo
Sign Up Now>>

Available through May 22, 2014

Trends in Safe Handling of Potent Compounds in Pharmaceutical Manufacturing Processes
Sponsored by: Patheon
Sign Up Now>>

Available through May 15, 2014

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

For questions contact Sara Barschdorf

Email Newsletters from Pharmaceutical Technology and Pharmaceutical Technology Europe
Providing the latest business, scientific, and regulatory news for the pharmaceutical and biotech industries. WEEKLY Archives Subscribe	Covers small and large- molecule pharmaceutical manufacturing, ingredients sourcing, and the pharmaceutical supply chain. MONTHLY Archives Subscribe	Focuses on pharmaceutical manufacturing processes and technology, featuring a showcase of processing equipment and reviews. MONTHLY Archives Subscribe	News from Europe's pharmaceutical manufacturing industry coupled with upcoming events, and exclusive articles and interviews from industry experts. WEEKLY Subscribe

Columnists
	sponsored by Outsourcing Outlook Eric LangerOutsourcing's Modest Role as a Cost-Containment Strategy
	sponsored by Ingredients Insider Patricia Van ArnumIntellectual Property Battles in Solid-State Chemistry
	sponsored by Industry Insider Nathan Jessop Campaign Against Counterfeit Drugs Continues
	Statistical Solutions Lynn D. TorbeckCompositing Samples and the Risk to Product Quality

Featured Jobs