2015 - Webinar On Good Documentation Practices

Description :
The webinar will discuss basic/key requirements for writing SOPs, recording data, completing forms and other basic documentation requirements for the GMP compliant company. Furthermore, the current industry requirements for recordkeeping will be discussed.
In this webinar,
You will be shown the benefits of good documentation practices in the GMP environment
You will gain a knowledge base for controlling and handling documents in a GMP compliant environment
You will have a better understand the basic requirements that FDA seeks for all records, documents, forms and procedures to meet GMP requirements
You will be guided on how to ensure the quality and consistency of processes/activities/manufacturing
Areas Covered in the Session :
Good Documentation Practices Do’s and Don’ts
cGMP requirements for changing and controlling entries into documents
Archiving of records
Current industry practices for GDP
Interactive Q&A Session
Who Will Benefit:
Quality Assurance Professionals
Quality Control Professionals
Regulatory Professionals
Pharma/Medical Devices/OTC Cosmetic Manufacturing Teams
Pharma/Medical Devices/OTC Cosmetic Packaging Teams
Pharma/Medical Devices/OTC Cosmetic Subcontractors
Contract Testing Laboratories
Owners/Presidents of GMP regulated companies
For more information about this event please visit
https://compliancetrainings.com/SiteEngine/Product...