Drugs (Humans and Animals) | Biologics | Food | Cosmetics | Dietary Supplements | Tobacco Products | Pharmacy Compounding | Medical Devices and IVDs

Social Media, Sales & Marketing | Big Data

LIVE | Good Social Media Practices to Avoid FDA Actions | Bi-Monthly, 2nd Fridays | 11:30 AM PST | 02:30 PM EST | 60 Minutes | Register Here
LIVE Big Data in FDA-Regulated Healthcare Industry: Best Practices for Systematic Use | Tri-Monthly, 2nd Thursdays | 10:00 AM PST | 01:00 PM EST | 60 Minutes | Register Here

Healthcare Business Practices

Developing and Implementing an Effective SOP in Healthcare Industry | Read More Here

FDA 510(k) Templates

FDA 510(k) Templates Ready for Use Compliant with eCopy and RTA Policy | Read More Here

LIVE Online Seminar Series

LIVE Online Seminar Series | Good Clinical Practice (GCP) | Register Here
LIVE Online Seminar Series | US FDA 510(k) Drafting | Register Here
LIVE Online Seminar Series | US FDA Premarket Approval (PMA) Drafting | Register Here
LIVE Online Seminar Series | Fundamentals of Regulatory Affairs for Drugs and Medical Devices |Register Here

Drugs

LIVE | Developing and Implementing a Global Regulatory Plan and Strategy | Monthly, 2nd Fridays | 01: 00 PM PST | 04:00 PM EST | 60 Minutes | Register Here
LIVE | Overview of the EMA Marketing Authorization Applications (MAAs) for Medicinal Products for Human Use in EU | Monthly, 2nd Mondays | 01: 00 PM PST | 04:00 PM EST | 60 Minutes | Register Here
LIVE | Quality Risk Management for Drugs and Biologics: Systematic and Holistic Approaches | Monthly, 2nd Mondays | 10:00 AM PST | 01:00 PM EST | 60 Minutes | Register Here
LIVE Online Seminar Series | Good Clinical Practice (GCP) | Read More Here

FDA Inspection Products

LIVEFDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers | Monthly, 2nd Mondays | 11:30 AM PST | 02:30 PM PST | 60 Minutes | Register Here
FDA Inspection Checklist to Avoid 483s for Drug Manufacturers | Learn More Here
FDA Inspection Checklist to Avoid 483s for Medical Device and IVD manufacturers | Read More Here

Recorded Online Seminars

Recorded | US Laws and Regulations for Medical Devices including In Vitro Diagnostic Devices (IVDs) | 78 Minutes | Read More Here
Recorded Complaint Handling and Medical Device Reporting (MDR) | 62 Minutes | Read More Here.  
RecordedRisk Management for Medical Devices and IVDs: Systematic and Holistic Approaches | 74 Minutes | Read More Here.