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May 13 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Jun 20 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Jul 8 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Sep 9 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Sep 19 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Nov 11 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Dec 19 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Jan 13 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Mar 9 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Mar 19 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
May 11 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Jun 18 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Jul 13 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Sep 14 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Sep 17 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Nov 9 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Dec 17 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Jan 11 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Mar 8 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Mar 18 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
May 10 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Jun 17 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Jul 12 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Sep 13 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Sep 16 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Nov 8 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Dec 16 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Jan 10 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Mar 14 @ 2:00 PM – 3:00 PM
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: May 13, 2019 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online seminar
Mar 17 @ 3:00 PM – 4:00 PM Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 20, 2019 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online