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Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Apr 8 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Jun 10 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Aug 12 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Oct 14 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Dec 9 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Feb 10 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Apr 13 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Jun 8 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Aug 10 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Oct 12 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Dec 14 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Feb 8 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Apr 12 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Jun 14 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Aug 9 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Oct 11 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Dec 13 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online
Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 @ Online or Your Office
LIVE Online Seminar Implementing an Internal Audit Program Compliant with ISO 13485 and 21 CFR Part 820 Date: June 15, 2017 NOTE: This seminar recurrs tri-monthly (every three month) on 3rd Thursdays. Your payment will apply for the next upcoming LIVE online
Feb 14 @ 2:00 PM – 3:00 PM
FDA Inspection Preparation and Readiness
LIVE Online Seminar FDA Inspection Preparation and Readiness: the Top 20 Most Common GMP Deficiencies for Device Manufacturers Date: June 12, 2017 NOTE: This seminar recurrs bi-monthly (every other month) on 2nd Mondays. Your payment will apply for the next upcoming LIVE online