Secrets to Writing Effective SOPs for Medical Device QMS

Overview:You will learn techniques for creating easy to read, clear, and concise SOPs that your employees can easily follow. Well written SOPs ensure that your employees understand and consistently follow processes. Well written SOPs send a message that your QMS is complete, accurate, and followed.
Why should you Attend:SOPs are one of the first things an auditor/ investigator will review during and inspection. Most importantly, poorly written procedures make it difficult for your employees to understand and consistently follow procedures. This can lead to disastrous consequences including quality problems and even recalls. Poorly written SOPs can and do impact your business.
Areas Covered in the Session:FDA Expectations for SOPsLessons Learned from 483s and Warning LettersCommon Problems and MistakesHow to Structure your QMS and SOPsHow to Outline and Format your SOPsUsing Process Maps to Make Procedures Clear
Who Will Benefit:Quality Systems SpecialistsDocument Control SpecialistsQuality and Compliance SpecialistsInternal Auditors and ManagersTraining SpecialistsCAPA Specialists
Speaker Profile:Susanne Manz MBA, MBB, RAC, CQA is an accomplished leader in the medical device industry with emphasis on quality, compliance, and six sigma. She has an extensive background in quality and compliance for medical devices from new product development, to operations, to post-market activities.
Event Fee: One Dial-in One Attendee Price: US $150.00
Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: support@compliance4All.com