Compliance to ISO 11607, Parts 1 and 2 require that Packaging Sterile Barrier Systems and Packaging Processes be validated. Validation planning is key to success. Inadequate planning will result in delayed time to market and ultimately financially negative impacts. Attend this webinar to obtain tangible and practical strategies and tactics for a successful medical packaging validation that you can put to immediate use.
Compliance to ISO 11607, Parts 1 and 2 require that Packaging Sterile Barrier Systems and Packaging Processes be validated. Validation planning is key to success. Inadequate planning will result in delayed time to market and ultimately financially negative impacts. Attend this webinar to obtain tangible and practical strategies and tactics for a successful medical packaging validation that you can put to immediate use.
Compliance to ISO 11607, Parts 1 and 2 require that Packaging Sterile Barrier Systems and Packaging Processes be validated. Validation planning is key to success. Inadequate planning will result in delayed time to market and ultimately financially negative impacts. Attend this webinar to obtain tangible and practical strategies and tactics for a successful medical packaging validation that you can put to immediate use. will be held in Fremont,United States on date 2015-01-14
Deadline for abstracts/proposals : 13th January 2015