Identification and Classification of Nonconformities in Glass Containers Training Course (PDA 283)
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This training course will provide manufacturers and users of glass containers with valuable knowledge related to the quality of glass containers including the types of defects associated with glass manufacture, the development of standardized quality criteria, and sampling plans for use in the quality decision-making process.
The development of PDA Technical Report, No. 43 (Revised 2013), Identification and Classification of Nonconformities in Molded and Tubular Glass Containers for Pharmaceutical Manufacturing and associated lexicons of glass nonconformities will be described to provide participants with a solid understanding of what is and isn’t in the report and why. Through a series of presentations accompanied by visual depictions of glass nonconformities, participants will be provided with a review of current best practices for identification and classification of visual nonconformities in glass containers. The training course will also present criteria such as the development and use of appropriate sampling plans for incoming inspection of glass containers and the appropriate application of acceptable quality limits for accept/reject decisions. The importance of the partnership between glass manufacturers and the pharmaceutical company using the glass containers in establishing glass container quality specifications will be emphasized.
Upon completion of this training course, the attendee will be able to:
- Summarize current best practices for identification and classification of visual nonconformities in glass containers
- Discuss the development and use of appropriate sampling plans for incoming inspection of glass containers and the appropriate application of acceptable quality limits for accept/reject decisions
- Describe the appropriate documentation and training for personnel involved in glass in section and disposition decisions
- Explain the importance of a partnership between glass manufacturers and the pharmaceutical company using the glass containers in establishing glass container quality specifications
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Marriott Crabtree Valley
4500 Marriott DrRaleigh, NC 27612 USA
Registration
Pricing Options
Early Registration
Register by 15 January 2025
Member Price
$899GovernmentMember Only
$699
Health AuthorityMember Only
$699
AcademicMember Only
$699
Non-Member
$1,079
Standard Registration
Register after 15 January 2025
Member Price
$999GovernmentMember Only
$699
Health AuthorityMember Only
$699
AcademicMember Only
$699
Non-Member
$1,199
GROUP REGISTRATION DISCOUNT: Register 3 people from the same organization as a group (at the same time) for the event and receive the 4th registration free. Other discounts cannot be applied.
GENERAL TERMS AND CONDITIONS: PDA will send you a confirmation letter within one week of payment being received. You must have this confirmation letter to be considered enrolled in a PDA event. If you have submitted a purchase order or requested an invoice, please be advised that a credit card guarantee is needed. PDA reserves the right to modify the material or speakers/trainers without notice or to cancel an event. If an event is cancelled, registrants will be notified by PDA immediately and will receive a credit (registration fee paid). PDA will not be responsible for any costs incurred by registrants due to cancellation. Please note that the attendee list is shared with attendees, trainers, and exhibitors and may be used to follow up on specific areas of interest after the event. Video, photo, and audio recordings are prohibited at all PDA events.
CANCELLATION: If a cancellation request is received 30 days before the event, a credit (registration fee paid minus a 200.00 USD/EUR processing fee) will be given. No credits will be given for cancellation requests received less than 30 days before the event. Cancellation requests must be emailed to registration@pda.org.
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