PDA 306 Technical Report No. 65: Technology Transfer
Registration Options
Individual Registration
Group Registration
This highly interactive training course, based on PDA Technical Report No. 65: Technology Transfer, will cover the business process and technical considerations for technology transfer of large and small molecules with principles that can be used for both drug substance and drug products.
Participants will learn about and have hands-on practice on the structure of a technology transfer, functional role requirements throughout a technology transfer, success factors, risk management, and documentation knowledge management. Participants will also receive a free copy of PDA Technical Report No. 65: Technology Transfer.
Upon completion of this training course, the attendee will be able to:
- Explain how the structure of a technology transfer enables success
- Know the functional role requirements throughout a technology transfer
- Understand success factors and their impact on risk assessment and risk management
- Differentiate between technology transfer types and approaches, such as internal versus external and clinical versus commercial
For more options and/or related training courses, please visit the following page(s):
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Early Bird Pricing
Register before 26 August 2024
Early Bird Member Price
$899GovernmentMember Only
$699
Health AuthorityMember Only
$699
AcademicMember Only
$699
Non-Member
$1,079
Standard Pricing
Register after 26 August 2024
Standard 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 [email protected].
Featured Trainers
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Beth J. Haas, MChE
Owner/Consultant, Haas Pharma Consulting
Read Bio
Beth J. Haas, MChE
Haas Pharma Consulting
With over 30 years in the industry, Beth has versatile experience across product lifecycle phases covering product development, CMC requirements, cGMP manufacturing, and CDMO management focusing on new product introductions and technology transfers for both APIs and drug products. She enjoys partnering with CDMOs across all platforms, working closely with procurement and supply chain to ensure compliance, and establishing strong relationships between the key functional areas to achieve regulatory approval. Beth is highly skilled in global team leadership, process development and engineering, quality risk management, GMP quality systems, and CMC regulatory filings. Currently, Beth is a member of the RAQAB, co-leads the Technology Transfer interest group for PDA, was a co-leader for the recently released PDA Technology Transfer technical report (TR-65), and was an author on the ISPE Technology Transfer guide, 3rd edition.
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