Compliance4All, Online Event
2016-05-05
Overview:
As long as increase in the regulatory requirements and market needs which causes conflicts between inspectional parties and manufacturers along with limited resources for each party, there must be a harmonized baseline between two parties that both must agree on. Upon achieving this harmonization, this will minimize the efforts that will in turn increase the quality of the product. Areas Covered in the Session: - Introduction to Qualification & Validation and discussion the Validation Lifecycl: This part includes introduction for the Validation including (but not limited to) what, why and when to Validate? As well as addressing the responsibilities for the validation. Also, this part will discuss the ideal LifecycSle for the systems undergoing the Q&V process so that audience will take good idea where exactly the Risk-Based can play essential role in this cycle.
- Introduction to the Risk based Q&V: During this part, there will be discussion about the risk based methodology to be used when qualification/validation new or existing systems, so that audience will take good idea about the keys of brainstorming to start implementing acceptable risk based approach prior starting the Qualification and Validation activities, upon implementing this successful and logic Risk-Based approach, this will reflect advantageous outcomes on both compliance and business wises as well.
- Case Study Discussion: Case Study will address the actual and live example that could be discussed to show how risk assessment is applied for a specific system , case study may include equipment or utilities.
Who Will Benefit:- Validation scientists manufacturing supervisors
- Equipment Engineers
- Engineering quality assurance specialists
- Professionals from service organizations and vendors who serve pharmaceutical clients
- Regulatory personnel involved in pharmaceutical industries.
- Pharmaceutical Project Manager
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