Events (Block Dates)
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14 May
2018 PDA Sterile Medicinal Products Manufacturing Conference
- 14 May - 15 May 2018 12:00 to 21:00 (Eastern Daylight Time (UTC -4))
The 2018 PDA Sterile Medicinal Products Manufacturing Conference will bring together sterile product experts and the sterile products community to highlight contemporary approaches for sterile product manufacturing. -
7 Jun
PDA Quality Culture Program - June
- 7 June - 8 June 2018 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
This program will provide you with the tools and knowledge to ensure that you collect verifiable data to create new processes that facilitate positive culture changes. -
13 Jun
2018 PDA Container Closure Performance and Integrity Conference
- 13 June - 14 June 2018 12:00 to 21:00 (Eastern Daylight Time (UTC -4))
The 2018 PDA Container Closure Performance and Integrity Conference will address the complexities and challenges to container closure performance and integrity. -
28 Jun
Best Compliance Practices at the GMP Testing Laboratory
- 28 June - 29 June 2018 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
This course provides detailed understanding regarding the implementation of respective cGMP requirements in a state-of the- art quality control laboratory in a pharmaceutical company. -
23 Aug
Quality by Design (QbD) for Biopharmaceuticals - A Practical Approach
- 23 August 2018 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
This course will discuss the importance and underlying principles of an effective QbD approach for biopharmaceuticals. -
27 Sep
Raw Material Requirements (FDA/Health Canada/ICH/USP/EP) in a CGMP Environment: Issues and Solutions - New Course
- 27 September - 28 September 2018 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
The objective of this two-day highly interactive course is to explore raw materials and their requirements – issues and solutions. -
10 Oct
2018 PDA Combination Products Workshop
- 10 October 2018 12:00 to 21:00 (Eastern Daylight Time (UTC -4))
Listen to the real life experiences of guidance from experienced pharmaceutical and Medical Device professionals detailing the challenges they have, or are currently facing -
11 Oct
Understanding Product Options, User Needs and Fill-Finish Requirements for Nested Format Syringes, Cartridge Containers and Drug Delivery Systems
- 11 October - 12 October 2018 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
This course will focus on providing a detailed understanding of the newest packaging technologies that support evolving drug and patient needs, considerations that must take into account, quality expectations to fulfill regulatory requirements, and how new manufacturing strategies are being applied to provide flexibility and decreased investments. -
11 Oct
Technical and Regulatory Challenges of Drug Delivery Combination Products - Prefilled Syringes, Autoinjectors and Injection Pens - October
- 11 October 2018 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
The course will examine the technical and regulatory challenges companies will face in the development and registration of drug delivery combination products. -
14 Oct
Prozesschromatographie
- 14 October - 17 October 2018 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
This course will be held in German. Dieser Kurs wird eine praxisorientierte Mischung aus Vorträgen, praktischen Experimenten und Simulationsübungen vermittelt, in allen Fällen mit der Möglichkeit zur Diskussion. Zuerst wird als Grundlage notwendiges, theoretisches Hintergrundwissen vermittelt, welches durch interaktive Tutorials an Hand von Beispielen vertieft wird. Sowohl achirale wie auch chirale Trennungen werden betrachtet. -
15 Oct
PDA Europe Pharmaceutical Microbiology
- 15 October - 16 October 2018 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
In 2018, this conference will be a truly global event! Taking place simultaneously in two different regions of the world, it will bring together industry, academic and regulatory experts to discuss Microbiology and its vast spectrum of possibilities. -
15 Oct
13th Annual PDA Global Conference on Pharmaceutical Microbiology
- 15 October - 17 October 2018 12:00 to 16:00 (Eastern Daylight Time (UTC -4))
The 13th Annual PDA Global Conference on Pharmaceutical Microbiology is designed to meet the unique needs of pharmaceutical microbiologists and interdisciplinary scientists involved in manufacturing and regulating the pharmaceutical industry. -
17 Oct
Rapid Microbiological Methods
- 17 October - 18 October 2018 13:00 to 21:00 (W. Europe Daylight Time (UTC 2))
This comprehensive course is designed to provide an intensive review of currently available rapid microbiological method (RMM) technologies, validation strategies, applications, regulatory expectations, financial justification models and implementation plans. -
17 Oct
2018 PDA Endotoxins Workshop
- 17 October - 18 October 2018 12:00 to 21:00 (Eastern Daylight Time (UTC -4))
The 2018 PDA Endotoxins Workshop will provide scientific understanding and real-world practices for endotoxin testing in bio/pharmaceutical production processes. -
18 Oct
Investigating Microbial Data Deviations
- 18 October 2018 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
This course will provide practical insights into both the regulatory and scientific considerations which must be taken when investigating microbiological data deviations. -
23 Oct
2018 PDA Cell and Gene Therapy Conference
- 23 October - 24 October 2018 12:00 to 21:00 (Eastern Daylight Time (UTC -4))
As part of PDA’s ongoing commitment to advanced therapies, the 2018 PDA Cell and Gene Therapy Conference will provide a broad overview of current innovations with a focus on what it takes to successfully steward these therapies toward approval and beyond. -
29 Oct
Process Validation: A Lifecycle Approach — Oral Solid Dosage/ Semisolid Dosage Forms Annex - New Course
- 29 October 2018 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
The participant will learn how to employ process understanding and quality risk management principles to the following three Process Validation concepts: Process Design, Process Qualification, and Continued (Ongoing) Process Verification (CPV). -
30 Oct
Development and Implementation of Qualification and Validation Protocols - A Risk and Science Based Approach
- 30 October - 31 October 2018 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
The objective of this course is to provide a basis by which the participant can develop and implement risk and science based approaches, as well as integrate and maintain programs, to qualify and validate biopharmaceutical and pharmaceutical systems and processes. -
1 Nov
2018 PDA Introduction to Artificial Intelligence (AI) in Biotechnology Operations Workshop
- 1 November 2018 13:00 to 16:25 (Malay Peninsula Standard Time (UTC 8))
This Workshop will give participants an introduction into the world of AI, including a review of its history and a framework for application. -
1 Nov
Analytical Method Qualification Validation, Verification, and Transfer for Biotechnological Products
- 1 November - 2 November 2018 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
This interactive course will provide a practical and detailed overview how to consistently perform risk-based analytical method qualification and validation for all method and product lifecycle steps.