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3rd Edition  Conference

Designing and Sustaining New and Existing Product Stability Testing Program


"Regulatory guidance associated with the requirements of a product’s stability testing program."
New or existing modified drug Stability Testing Program's regulations/requirements stipulated by the FDA, 21 CFR or other regulations may sometimes creating an overwhelming situation based on the type of product that is being manufactured. Hence, some manufacturers of new drug products have made inadvertent mistakes in the design of their new drug stability testing program.

Highlights

  • Regulatory guidance associated with the requirements of a product’s stability testing program.
  • Using the Laboratory Information Management Systems (LIMS) in a Stability Study Program
  • Data Documentation, Entry and Management (Types of Documentation Methods)
  • The Criticality of the Choice of a Stability Test Data Management System used for Data Management.
  • Considerations when choosing a Stability Test Data Management System

Timings

8:00 AM - 5:00 PM (Feb 13) (General)
8:00 AM - 5:00 PM (Feb 14) (General)

Entry Fees

Paid Ticket Starts from 2099 USD View Details

Participants

20
Delegates

5 Exhibitors Estimated Count

Category & Type

Conference
Medical & Pharma

Editions

13 - 14 Feb 2020 Interested
15 - 16 Feb 2018 2nd Edition
23 - 24 Jun 2016 1st Edition
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Frequency Bi-annual

Official Links

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ComplianceOnline USA

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Visitor Ticket Price Buy Now

2099 USDAttendee Seminar One Registration
37.775000 -122.419000

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San Francisco, USA

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