Events (Block Dates)
-
16 Mar
Track and Trace: How to implement Pharma Serialization, Tamper Evidence and the EU-Falsified Medicines Directive
- 16 March - 17 March 2017 13:00 to 20:00 (W. Europe Standard Time (UTC 1))
It is the course’s goal to inform about the latest developments in serialisation & authentication coming from the EU directive 2011/62/EC and the corresponding Delegated Regulation as published in the Official Journal of the European Union. -
3 Apr
Praxis der Pharmazeutischen Gefriertrocknung
- 3 April - 7 April 2017 14:00 to 22:00 (W. Europe Daylight Time (UTC 2))
Please notice that this training course will be held in German!! Aufbau und Funktionsprinzip von Gefriertrocknern werden vorgestellt und das Zusammenspiel der verschiedenen Funktionsgruppen wird erklärt. Sie lernen die regulatorischen Anforderungen an den Gefriertrocknungsprozess kennen. Die Umsetzung dieser Anforderungen sowie die Darstellung des Prozessablaufs wird an Beispielen von Chargendokumentationen vorgestellt. -
6 Apr
Quality Strategy for Biopharmaceuticals
- 6 April - 7 April 2017 12:30 to 20:00 (Pacific Daylight Time (UTC -7))
This course will provide insights and practical guidance for those responsible for determining and assuring the required quality for biopharmaceuticals for human use. -
6 Apr
Quality Metrics and Quality Culture
- 6 April - 7 April 2017 12:30 to 20:00 (Pacific Daylight Time (UTC -7))
With the recent interest of FDA in quality metrics, our industry is recognizing that measuring process performance and subsequently taking action to improve the processes is the way to improve quality and significantly reduce costs at the same time. -
6 Apr
Knowledge Management Applied in Facilities & Engineering to Improve Manufacturing Reliability
- 6 April - 7 April 2017 12:30 to 20:00 (Pacific Daylight Time (UTC -7))
This course will engage participants in a common goal of effecting positive change and improving equipment, facility, and utility reliability through facilities and engineering. -
18 Apr
Regulatory and Compliance Course Series
- 18 April - 21 April 2017 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
-
19 Apr
Environmental Control and Monitoring for Regulatory Compliance
- 19 April 2017 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
This comprehensive class will discuss facility design and validation, including personnel flow, equipment flow, baseline monitoring, media fills and quality control. -
26 Apr
Current Trends in Aseptic Fill & Finish of Pre-filled Syringes
- 26 April - 27 April 2017 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
The conference is held from 26-27 April in Lindau/Bodensee (Lake Constance) in Germany and gives you a broad overview of current best practice in Aseptic Processing with a focus on Fill & Finish of pre-filled syringes, including the current technical and regulator trends. -
3 May
Basics of Successful Auditing
- 3 May - 4 May 2017 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
The course consists of two parts: The participants will be provided with all information around the audit as laid down in the regulations and technical best practices. The other part will extensively cover the communication techniques during an audit, especially how to lead an audit, conflict situations, communication pitfalls. -
22 May
Lyophilization Course Series
- 22 May - 25 May 2017 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
Learn about the development of lyophilized products and the validation of Lyophilization processes by attending PDA Education’s Lyophilization Course Series. -
29 May
Pre-Conference Workshop: The Principles of Viral Safety for Biologics and Vaccines
- 29 May 2017 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
This workshop will provide an overview of two important viral safety barriers – testing and viral clearance approaches for recombinant products and vaccines. Typically applied testing methods and product type specific testing strategies will be presented briefly. The benefits and the downsides will be discussed based on the experiences gained over a period of more than 20 years. -
12 Jun
Cleaning and Disinfection
- 12 June 2017 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
This interactive course deals with all aspects of cleaning and disinfecting a sterile manufacturing facility. The information shared will encompass regulatory aspects, Environmental Monitoring, contamination sources, selection of disinfectants and cleaning agents, the validation and how they should be used properly. -
12 Jun
Business Opportunities in Iran
- 12 June 2017 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
Following the success of the first PDA Conference in Tehran (Iran) in September 2016, PDA Europe is organizing the workshop “Business Opportunities In Iran” previously to the 2nd PDA Europe Annual Meeting. -
12 Jun
Quality by Design for Biopharmaceuticals
- 12 June 2017 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
Gain a firm understanding to apply the principles of QbD to all types of biologic products –recombinant proteins, monoclonal antibodies, biosimilars, gene therapy products and cell-based medicines. -
13 Jun
2nd PDA Europe Annual Meeting
- 13 June - 14 June 2017 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
After the tremendous success of the First PDA Europe Annual Meeting, we look forward to the second edition of this conference in Berlin, Germany, 13 – 14 June. Under the title “Manufacturing 4.0”, a broad range of topics will be covered, from flexible facility design to self-optimizing processes, from Big Data to packaging. -
19 Jun
Biotechnology Course Series
- 19 June - 22 June 2017 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
-
20 Jun
Environmental Monitoring Course Series - June
- 20 June - 22 June 2017 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
Take 10% off when you register for both courses! -
22 Jun
Biopharmaceutical QA/QC Strategy for Senior Management
- 22 June 2017 12:30 to 20:00 (Eastern Daylight Time (UTC -4))
This course will provide insights and practical guidance for senior management in evaluating the effectiveness of their QA/QC strategy for biopharmaceuticals. -
26 Jun
Practical Application of Phase-Appropriate GMP & Quality Principles to Clinical Development of ATMPs
- 26 June 2017 13:00 to 22:00 (W. Europe Daylight Time (UTC 2))
Prior the two-day conference, this training course will look at the practical application of GMP for development of APIs. -
13 Sep
Quality Metrics and Quality Culture for Pharmaceutical Manufacturing - Australia
- 14 September - 15 September 2017 12:30 to 20:00 (AUS Eastern Standard Time (UTC 10))
Participants will examine their quality management system, select the appropriate quality metrics that drive intended behaviors, and determine how best to collect and use the data to improve the quality system using the ICH Q10 guidance as framework for a practical and suitable methodology.