Horst Koller, Member of Ph. Eur. Plastic Packaging Expert Groups at the EDQM (EP CGE 16), HK Packaging Consulting, Switzerland
The quality of plastic materials has an impact on the quality of plastic containers for pharmaceutical use and thus on the medicinal product. Of particular relevance are the widely used plastic materials COP (cycloolefin polymer) and COC (cyclo-olefin copolymer). In the recent issue of Pharmeuropa drafts for three new Ph. Eur. chapters on plastic materials have been published for comment (public deadline: 30 June 2020):
- 3.1.16. Cycloolefin-Polymere (COP)
- 3.1.17. Cycloolefin-Copolymere (COC)
- 2.4.35. Extractable elements in plostic materialsfor pharmaceuticol use
The new Ph. Eur. chapters give specifications for COC / COP materials, used, for example, in the manufacture of prefillable syringes. According to Pharmeuropa, they “follow the same structure as other general chapters on plastic materials in Ph. Eur. Subsection 3.1.”. However, there are two major changes in relation to the existing chapters:
- Additives.It is clarified that “The supplier of the material must be able to demonstrate that the qualitative and quantitative composition of each production batch complies with that of the type sample.”
- Extractable Elements: The proposed monographs include the testing for
- Specific elemental impurities,
- Elemental impurities that are common to various plastic materials currently on the market. They are to be controlled according to the new general Ph. Eur. chapter 2.4.35. Extractable elements in plastic materials.
In comparison, the new USP Chapter <661.1> Plastic Materials of Construction states: “it is being left up to the material user to evaluate the need for extractable elements testing and, if such testing is necessary, to establish and justify the means by which testing is accomplished”.
This webinar will provide a detailed update on the recent developments in the area of these plastic packaging materials.
Members of staff and executives from the pharmaceutical industry working in the field of research and development, regulatory affairs, quality control, incoming goods control of packaging materials, quality assurance, production and packaging. Employees of suppliers and/or manufacturers of plastic packaging materials for the pharmaceutical industry.
To participate in an on demand training course or webinar, you do not need any software. The recordings are made available via a streaming server. In general, the recording is provided in MP4 format, which any PC (Microsoft Windows, Apple IOS) or tablet can easily display.
Timing and Duration:
When you register for the on demand Training course or webinar you can decide at what date you want to follow the training course online. For a 1-day training course you will have 2 days in which the stream is available (for 2-day training course 3 days and for a 3-day training course 4 days). Within in this timeframe you can start & stop the stream according to your needs.
In time before the scheduled date (your desired date) you will receive an e-mail from us with a link for direct participation as well as your log-in data.
Training Course Documentation and Certificate:
The presentations will be made available as PDF files via download shortly before the online training course. After the event, you will automatically receive your certificate of participation.
- COP and COC Plastic Materials in the Pharmaceutical Industry
- Chemical and Physical Properties
- Application examples
- Pharmacopoeial Compliance Testing (USP / Ph. Eur.)
- Extractable Elements
- Question and Answers
Recording from 8 June 2020
Duration of recording: about 1,5 h.