Webinar On How to Develop a Master Validation Plan
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| Description: | This webinar on “How to Develop a Master Validation Plan” (also known as Validation Master Plan) will provide a step-by-step procedure for all medical device companies and their suppliers that are in need of developing a plan for product/equipment transfer, facilities, processes or to develop a company standard. Areas Covered in the Session : Master Validation Plan content Revision history Background Objective Purpose Scope Project approach Key activities Project organization Communication plan Quality Assurance Facility approach Validation approach Schedule Budget ...and more Who Will Benefit: OEM Senior management Supplier Senior management Managers and directors Managers setting up new facilities and product lines Plant and facility managers End-users responsible for design control and product development R&D and product development Project managers Facility and clean room designers Process engineers and managers Validation engineers Quality management and engineers Auditors Suppliers to medical OEM’s Consultants |
| URL: | https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=MD1186 |
| Date: | Tuesday, January 27, 2015 |
| Time: | 6:00pm-7:00pm UTC |
| Duration: | 1 hour |
| Access: | Public |
| Category: | Webinar* |
| Created by: | Public Access |
| Updated: | Tuesday, December 16, 2014 12:01pm UTC |
| : | $249 |
| : | 4169154458 |
| : | uttam@compliancetrainings.com |
| : | Uttam Mandal |
| : | 4169154458 |
| Comments: | None |