Falls Church, VA (PRWEB) March 03, 2022 FDA Medical Device Inspections in the Postpandemic World:Are You Ready for New Approaches and Methods?An FDAnews
FDAnews Announces On-Site Inspections: They’re Back But When, Where and How Webinar August 12, 2021
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How will the clinical trial industry merge on-site audit and virtual inspection best practices? Find out how by registering today.
WCG FDAnews On-Site Inspections:
An FDAnews Webinar
The development and distribution of COVID-19 vaccines have helped the global health crisis take a positive turn in some parts of the world. This change has many manufacturers pushing to shift some practices back to pre-pandemic norms including a return to on-site inspections and audits.
How can drug and devicemakers effectively merge the best practices for conducting on-site and virtual inspections?
FDAnews Announces Effective Auditing for Manufacturing Quality Webinar Feb. 17, 2021
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WCG FDAnews Effective Auditing for Manufacturing Quality
An FDAnews Webinar
Learn to identify and correct issues before they impact operations. Run processes and business smoothly.
Gain confidence that the product meets the necessary quality standards and ensure compliance. Susan Schniepp has 40 years of high-level quality assurance experience in the pharmaceutical industry. Susan will lead a 90-minute panel discussion with Seyed Khorashahi and Steve Lynn from Regulatory Compliance Associates® Inc. The panel will help attendees prepare, organize and streamline the audit approach so one can identify quality issues or work with clients on solutions to establish a more robust operation that stands up to regulatory scrutiny.