Канал: FDAQRC

Connect Profile Creation Overview

Cync Client Portal Training

Cync Client Portal Training

SpringAhead Training

SpringAhead Training

Service Execution Process Map Overview

Service Execution Process Map Overview

Important Regulatory Updates from 2019 – ISO Focus

Important Regulatory Updates from 2019 – ISO Focus

Important Regulatory Updates from 2019 – eSystems Focus

Important Regulatory Updates from 2019 – eSystems Focus

Important Regulatory Updates from 2019 – Good Manufacturing Practices

Important Regulatory Updates from 2019 – Good Manufacturing Practices

Important Regulatory Updates from 2019 – Medical Device Focus

Important Regulatory Updates from 2019 – Medical Device Focus

Important Regulatory Updates from 2019 – Good Pharmacovigilance Practices

Important Regulatory Updates from 2019 – Good Pharmacovigilance Practices

Important Regulatory Updates from 2019 – International Focus

Important Regulatory Updates from 2019 – International Focus

Important Regulatory Updates from 2019 – Good Laboratory Practices

Important Regulatory Updates from 2019 – Good Laboratory Practices

Important Regulatory Updates from 2019 – Good Clinical Practices

Important Regulatory Updates from 2019 – Good Clinical Practices

Webinar: Assent and Consent in Clinical Research for Children

Webinar: Assent and Consent in Clinical Research for Children

Consultant Spotlight: Interview with Dennie Grabow

Consultant Spotlight: Interview with Dennie Grabow

Medical Device Product Development from Concept to Reality

Medical Device Product Development from Concept to Reality

Consultant Spotlight: Interview with Mugdha Dixit

Consultant Spotlight: Interview with Mugdha Dixit

Due Diligence in GxP Supplier Selection Webinar

Due Diligence in GxP Supplier Selection Webinar

Consultant Spotlight: Interview with Donna McElcar

Consultant Spotlight: Interview with Donna McElcar

2018 Medical Device Regulation EU 2017/745 Training v1.0

2018 Medical Device Regulation EU 2017/745 Training v1.0

2018 Good Manufacturing Practices Training v1.0

2018 Good Manufacturing Practices Training v1.0

2018 Good Laboratory Practices Training v1.0

2018 Good Laboratory Practices Training v1.0

2018 21 CFR Part 11 e_Records & Mobile Technology Training v1.0

2018 21 CFR Part 11 e_Records & Mobile Technology Training v1.0

2018 ICH GCP E6 R2 Training v1.0

2018 ICH GCP E6 R2 Training v1.0

2018 ISO 13485 2016 Training v1.0

2018 ISO 13485 2016 Training v1.0

483 Responses: Do you Have It What It Takes Webinar

483 Responses: Do you Have It What It Takes Webinar

2018 Good Pharmacovigilance Practices Training v1.0

2018 Good Pharmacovigilance Practices Training v1.0

Important Updates from 2018 – GCP and PV v1 0

Important Updates from 2018 – GCP and PV v1 0

Important Updates from 2018 – CSV and Privacy v1 0

Important Updates from 2018 – CSV and Privacy v1 0

Important Updates from 2018 – GcLP and GLP v1 0

Important Updates from 2018 – GcLP and GLP v1 0

Important Updates from 2018 – Regulatory and Device v1 0

Important Updates from 2018 – Regulatory and Device v1 0

Important Regulatory Updates from 2018 Webinar

Important Regulatory Updates from 2018 Webinar

FDAQRC Live Stream

FDAQRC Live Stream

Consultant Spotlight: Interview with Michelleanne Bradley

Consultant Spotlight: Interview with Michelleanne Bradley

Are You Inspection Ready Webinar

Are You Inspection Ready Webinar