Ensuring a successful clinical trial requires a keen understanding of each step involved. From drug procurement and analytical testing requirements, to batch records and production through the primary and/or secondary packaging requirements, this one-hour on-demand webcast will provide an overview of the criteria you'll need to avoid the pitfalls of outsourcing.

Listen to industry experts review case studies which explain how to ensure clinical trial success for biotech and pharmaceutical companies. Highlights include:

• Recommended manufacturing choices;
• Packaging considerations;
• Specific analytical method development and method validation processes.

An Excellent Learning Experience
If you have an upcoming trial and need to understand the design hurdles of outsourcing clinical drug manufacturing tune in and learn:

What known industry experts think about manufacturing using overencapsulation

How to identify multiple project timelines well in advance to effectively plan and manage your outsourced clinical trial

The analytical requirements used to successfully plan for outsourcing a clinical trial




Presented by:

In Association with:

On-Demand Webcast
Duration: 1 hour

Featured Webcast Speakers

Moderator:
Mike Auerbach
Editor-in-Chief
PHARMACEUTICAL PROCESSING


Panelists:

Mike Auerbach will be joined by a panel of experts including:

Martin L. Jeiven
MS,RPh, President
Jeiven Pharmaceutical Consulting

Robert G. Myers
Director of Clinical Manufacturing
Fisher Clinical Services

Gregory P. Kushla
Director, Clinical Supply Operations
Daiichi Sankyo Pharma Development