Organize and Presented By
247compliance
Sponsored By
247compliance
Organizing/Related Departments
Medical Device Resource
Organization Type
Event Organizing Company
WebinarCategory
Non Technical
WebinarLevel
All (State/Province/Region, National & International)
Related Industries
Medical/Healthcare/Hospital
Location
Newark, Delaware, United States
Almost every paragraph of the Quality System Regulation says that manufacturers shall “establish” procedures. This webinar will help you to write complete, clear, unambiguous, and flexible SOPs that accomplish that objective. You will learn techniques for creating concise and easy to read SOPs that your employees can understand and will follow. Well written the SOPs ensure a result in more consistent process output and quality results.
Standard Operating Procedures (SOPs) are a critical ingredient in an effective and efficient Quality Management System. SOPs are typically one of the first things an investigator asks for in an inspection. Well written SOPs send a message to the FDA and Notified Bodies that your QMS is complete, accurate, and followed. More importantly, well written SOPs ensure that your personnel can consistently and accurately follow your processes, resulting in correct outcomes and quality work.
- LEARNING OBJECTIVES
- Overview of the regulations
- FDA expectations
- Lessons learned and common mistakes
- Best practices
- Preparing for an FDA inspection
“Inadequate SOP” observations still rank among the most frequently cited 483 and Warning Letter observations. SOPs are one of the first things an auditor/ investigator will review during an 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.
- FDA expectations for SOPs
- Lessons learned from 483s and warning letters
- Common problems and mistakes
- How to structure your QMS and SOPs
- How to outline and format your SOPs
- Should, Shall, May, Do Not, Guidance
- Complete and concise
- Using process maps to make procedures clear
- Using diagrams and visuals
- Maintaining and controlling SOPs
- Ensuring adequate training to your SOPs
- Best practices
- Quality Engineers
- Compliance Specialists
- CAPA Managers
- Complaint Handling Managers
- Compliance Managers or Directors
- Quality Managers or Directors
- Process Owners
- Business Leaders wishing to present a professional and compliant organization
Registration Fees
Available
Registration Fees Details
Live session for 1 participant
$199
Live + Recorded Session
$269
Live + Transcript
$249
Live + Training CD
Free shipment within 72 hours from the date of webinar completion.
$450
On Demand Options
Transcript
$179
Downloadable recorded session
$239
Training CD
Free shipment within 72 Hours, from the date of webinar completion
$350
Group Session unlimited participants + Recorded
$799
Registration Ways
Email
Phone
Website
Other
Address/Venue
247compliance
2035 Sunset Lake,
RoadSuite B-2,
Newark,
Delaware - 247compliance
Pin/Zip Code : 247compliance