globalcomplianceseminar.com
Developing and Implementing an Effective SOP in Healthcare Industry |
https://www.globalcomplianceseminar.com/event/developing-and-implementing-an-effective-sop-in-healthcare-industry
Helping Industry Think and Execute Easier and Better. Developing and Implementing an Effective SOP in Healthcare Industry. Add to Timely Calendar. Add to Apple Calendar. Add to other calendar. January 22, 2016 @ 2:00 PM 3:00 PM. Writing an Effective SOP. Developing and Implementing an Effective SOP in Healthcare Industry. Date: January 22, 2016. This seminar recurrs tri-monthly (every three month). Your payment will apply for the next upcoming LIVE. Time: 11:00 AM PST 02:00 PM EST. Ccurate, and C. In thi...
globalcomplianceseminar.com
Complaint Handing and Medical Device Reporting |
https://www.globalcomplianceseminar.com/event/complaint-handing-and-medical-device-reporting-mdr
Helping Industry Think and Execute Easier and Better. Complaint Handing and Medical Device Reporting. Add to Timely Calendar. Add to Apple Calendar. Add to other calendar. January 14, 2016 @ 4:00 PM 5:00 PM. Global Compliance Seminar (GCS). LIVE Online Seminar LIVE Webinar. Medical Devices and IVDs. Title: Complaint Handling and Medical Device Reporting (MDR). January 14, 2016. This seminar recurs bi-monthly. 01:00 PM PST 04:00 PM EST. About the Areas to Be Discussed. Applicable Laws and Regulations.
regulatorydoctor.us
510k Information | FDA Regulatory Consulting Services
http://regulatorydoctor.us/510k-information
Was successfully added to your cart. 21 CFR Food Drugs. Medical Device Certificate Application. FDA GLP Inspection Guidance-21 CFR Part 58. EMA Quality Pharmaceutical Development. 21 CFR 820.198 Complaint Files. 21 CFR Part 211 Current Good Manufacturing Practice. 21 CFR Sec. 820.30 Design Controls. 510k EU CE Marking Consultants. 21 USC Controlled Substances Act. Drug Approval: Stivarga, regorafenib. EU Guide: Clinical Trials Clinical Trials Applications. EU Marketing Authorization Application. Premarke...
globalcomplianceseminar.com
Implementing Global Medical Device Adverse Event Reporting Systems |
https://www.globalcomplianceseminar.com/event/implementing-global-medical-device-adverse-event-reporting-aer-systems-eu-canada-us
Helping Industry Think and Execute Easier and Better. Implementing Global Medical Device Adverse Event Reporting Systems. Add to Timely Calendar. Add to Apple Calendar. Add to other calendar. September 5, 2016 @ 2:00 PM 3:00 PM. LIVE Online Seminar (LIVE Webinar). Adverse Event Reporting Systems. Implementing Global Medical Device Adverse Event Reporting (AER) Systems in EU, Canada and US. Date: September 5, 2016. This seminar recurrs tri-monthly (every three month). Time: 11:00 AM PST 02:00 PM EST.
globalcomplianceseminar.com
Fundamentals of Regulatory Affairs for Drugs and Medical Devices
https://www.globalcomplianceseminar.com/fundamentals-regulatory-affairs-drugs-medical-devices
Helping Industry Think and Execute Easier and Better. Fundamentals of Regulatory Affairs for Drugs and Medical Devices. Online Programs in Regulatory Affairs. The Fundamentals of Regulatory Affairs for Drugs (“ Drug Program. Medical Devices (“ Device Program. Each class consists of 60-minutes of online seminar (LIVE or recorded). There are four classes for each program. Begins on the First Mondays. Of January, March, May, July, September, November. 10:00 AM PST 01:00 PM Flexible Scheduling 60 Minutes.
globalcomplianceseminar.com
Overview of the EMA Marketing Authorization Applications for Medicinal Products |
https://www.globalcomplianceseminar.com/event/overview-of-the-ema-marketing-authorization-applications-maas-for-medicinal-products
Helping Industry Think and Execute Easier and Better. Overview of the EMA Marketing Authorization Applications for Medicinal Products. Add to Timely Calendar. Add to Apple Calendar. Add to other calendar. June 13, 2016 @ 11:00 AM 12:00 PM. 731-Go to GCS (468-6427). EU Marketing Authorization Application (MAA). EU Marketing Authorization Application (MAA). Overview of the EMA Marketing Authorization Applications (MAAs) for Medicinal Products for Human Use in EU. Date: June 13, 2016. Marketing authorizatio...
passfda.com
[CDC] Salt Matters
http://passfda.com/video/cdc-salt-matters
Quest for Regulatory Compliance. Providing Healthcare and Medical Information. FDA Approved Drugs for Insulin. Nuclear Plant Radiation and Risk. Learn About Deep Vein Thrombosis and Pulmonary Embolism. Educational Video] Robotic Prostatectomy. Face Transplant Surgery Story. Medical Video] Attention Deficit Hyperactivity Disorder (ADHD). What Is Vascular Dementia? On the Go with Diabetes. Medical Video for Parkinson’s Disease. Hereditary Breast and Ovarian Cancers: Genetic Testing. Source: National Center...
regulatorydoctor.us
Services | FDA Regulatory Consulting Services
http://regulatorydoctor.us/services
21 CFR Food Drugs. Medical Device Certificate Application. FDA GLP Inspection Guidance-21 CFR Part 58. EMA Quality Pharmaceutical Development. 21 CFR 820.198 Complaint Files. 21 CFR Part 211 Current Good Manufacturing Practice. 21 CFR Sec. 820.30 Design Controls. 510k EU CE Marking Consultants. 21 USC Controlled Substances Act. Drug Approval: Stivarga, regorafenib. EU Guide: Clinical Trials Clinical Trials Applications. EU Marketing Authorization Application. 21 CFR Food Drugs. EU ( European Commission.
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