Release of ISO9001:2015

trainingGood discussion on LinkedIn from Robert Packard

 https://www.linkedin.com/groupItem?view=&gid=2070960&type=member&item=5966251719061970949&trk=Skyline_click_NGDR&sl=NGDR%3B38756144%3A1423032125425%3B0%3B%3B

Making change happen

Making change happen

The 2015 version of ISO 9001 is expected to be released in October of this year (http://bit.ly/ISO9001-revision). We also expect the ISO 13485 Standard to be revised shortly after the release of the 2015 version of 9001. Manufacturers will need to update their quality system to comply with the new version of either Standard. There are two big questions related to the 9001 change: …..

 

Clean rooms for medical devices

The requirements for production of medical devices is going to get more stringent and comprehensive due to imminent regulations; as is the case in Europe, Australia and the USA. The cleanliness requirement of the environment and facility will be dependent on the type, stucture and format of the medical device, it’s packaging and manufacturing process. This is where clean room design, layout and validation is becoming more applicable. To quote WHO “– clean area – An area with defined environmental control of particulate and microbial contamination, constructed and used in such a way as to reduce the introduction, generation, and retention of contaminants within the area.”

 

Contact Simone on

082 871 5740
simone@isohealthsa.co.za


Removing RISK by linking business to ISO standards, legal compliance and GBP(Good Business Practice)

Contact Rudolph-Shortt Consultancy



Joint venture for project management GMP renovations and new facilities

Compliance Projects


R-SC Training

CLICK FOR TRAINING NEEDS AND APPLICATION