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This workshop will bring together industry professionals to network and benefit from updates on recent regulatory guidance’s regarding developing and validating analytical methods. It will provide participants with a comprehensive review of laboratory and documentation standards expected during the development, qualification, validation, and transfer of analytical methods. All attendees will receive a free electronic copy of PDA Technical Report No. 57, Analytical Method Validation and Transfer for Biotechnology Products.

Contact the event managers listed below for more information about how you can participate at the 2013 PDA Analytical Methods Development & Validation Workshop.

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Conference/Event Dates: 10/07/2013 - 10/08/2013
Classification: B2B
Primary Industry: Pharmaceutical
Other Industries: Pharmaceutical
Estimated Attendance: 200
Audience: Departments: QA/QC, CMC Project Managers and Technical Experts, CMC Regulatory Reviewers, Regulatory Affairs, Pharmaceutical, Chemical, Biotechnological and Analytical Development, Bio Pharmaceutical Development, Validation, Compliance, Engineering, Manufacturing, Research and Development, Manufacturing Outsourcing Managers, CMO Managers and Scientists

Level of Expertise: Executives, Management, Supervisors, Scientists/Technicians
Venue: Renaissance Baltimore Harborplace Hotel
Venue Phone: (410) 547-1200
Venue Type: Indoor - Hotel
Conference Hotel URL:official hotel URL
Sponsorship: Yes

Booth Size Booth Cost   Available Amenities
Call for information.   Electricity: n/a
  Water: n/a
  Generator: n/a
  Marketing Vehicles Allowed: n/a
Other Booth Sizes Available: n/a

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2013 PDA Analytical Methods Development & Validation Workshop

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