Quality professional training

03/01/2024

19/10/2023

Worth watching 🙂

What is ISO 15378 Certification | Primary Packaging Material for Medical DeviceTopic Cover:1. What is ISO 15378 - Primary Packaging Material for Medical Devi...

23/11/2021

If anybody interested

https://www.facebook.com/102368254933073/posts/396981608805068/

01/01/2020

Our January training session
"Quality Risk Managment"

With the intelligent instructor

Marwa El Mahdy
"Master of Total Quality Managment"

Details for reservation will be soon 😉

Happy New year !

01/01/2020

Happy new year every one
Wait our new programme for 2020 😊😉

09/02/2019

ISO 9001:2015 & cGMP similarities
Both require:
• Written records and procedures appropriate to the processes taking place
• A control process for these records and procedures
• That personnel are properly trained and qualified to perform their jobs
• That work environments are properly maintained
• That customer complaints and nonconformances are addressed, and that appropriate corrective actions are taken to prevent recurrences
• That equipment be maintained and calibrated
• That products be properly identified throughout the manufacturing cycle
• That there be product release procedures , analysis of product, and conformance to specifications prior to release
• Appropriate quarantining and control of nonconforming product to prevent its release to the marketplace
• The application of good scientific principles and statistical techniques
also risk base thinking (differ in implementation but spirit is similar .

join our sessions for ISO 9001 :2015 awareness and implementation
also offer valuable sessions for advanced cGMP.
reserve through our page.

08/02/2019

good morning
DOCUMENTS AND RECORDS
it is important to distinguish between the concepts of documents and records.
Documents ,in GMP environment ,refers to how -to instructions that outline what needs to be done to produce the product or operate in compliance with the regulations.
Records,in GMP environment refers to the body of information (history ) or data related to the manufacturing ,packaging,testing,and holding of each batch of finished product .
once a document has data written on it , it becomes a record.
Do not miss our valuable session for document control.
for reserve :- call our page.

05/02/2019

5S and Red Tag system

05/02/2019

How to implement 5S lean
Don’t miss our session

05/02/2019

non conformity investigation is an important task in QMS ,
Don't miss our sessions for handling of deviations.
contact us for more details.