Medical Device and Healthcare Technology: Quality & Compliance Manuals, Checklists & more - ComplianceOnline.com
Medical Device and Healthcare Technology
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Medical Device Quality Manual - quality control manual for manufacturers of medical devices providing compliance with ISO 13485:2003, ISO 9001:2000, Canadian CMDCAS requirements, Medical Device Directive 93/42/EEC of the European Union and Quality System.
Provider: Quality-Control-Plan Shipping: Available for download - Link will be provided in My ComplianceOnline section
This FDA compliance webinar will evaluate the FDA expectations
in the near term and further out in the future and how it will boil down to new regulatory climate.
This Project Management training for FDA Regulated Companies will show how you can meet key FDA and EU MDD regulatory requirements for the project you manage. It will focus on proven tools and techniques for successful development and implementation of project management planning.
