Requirements for pharmaceutical QC laboratories MasterClass - EU edition
02-03 November, 2023
This masterclass will provide a comprehensive overview on any of the topics relevant in this context
It is not uncommon for marketing authorisation holders to use external testing facilities within the framework of quality control and stability testing of active substances and medicinal products, possibly also including batch release.
02-03 November, 2023, Virtual
Time Zone: UTC/GMT+1 /CET
It is not uncommon for marketing authorisation holders to use external testing facilities within the framework of quality control and stability testing of active substances and medicinal products, possibly also including batch release. These may be laboratories of contract manufacturers or independent laboratories that perform such tests in toto or in part. In the light of a number of recent developments, updates and revisions of guidelines and new requirements, it seems appropriate to consider in detail the resulting consequences for the qualification, auditing and monitoring of contract laboratories. In this masterclass we provide a comprehensive overview on any of the topics relevant in this context.
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Who should attend?
• Persons involved in the subcontracting of quality control activities and respective supplier qualification and audits
• QA managers responsible for external partners
• Qualified persons certifying appropriate processes and contracts in place in the course of batch release
• Any QC personnel involved in quality control and stability testing
"High attention to detail in course content and very well delivered"
Product Development Manager
"Very good training led by two knowledgeable and open experts. Excellent insight given on many complex topics. Interactive and highly useful"
USP PD Team Manager
"Great course, impressed with the knowledge of the trainers and ability to answer wide variety of questions!"
Manager, Senior Investigator
MT Sword Laboratories (BMS)
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