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