Daniel Houde Email & Phone Number
Head, Clinical Quality Assurance @ Seriant (formerly MHICC)
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Daniel Houde Location
- Terrebonne, QC, CA
Daniel Houde Work
- 2025 -now Head, Clinical Quality Assurance @
- 2023 -2024 Senior Director, Clinical Quality Assurance @
- 2022 -2023 Director Of Quality Assurance @
- 2019 -2022 Director, Development Quality Assurance @
- 2018 -2019 Senior Director Clinical Studies @ Medicago
- 2017 -2018 Head, Clinical Compliance and Training @
- 2016 -2017 Head of Quality Assurance and Compliance @ Cara Therapeutics
- 2015 -2016 Senior Director, Regulatory Policy and Compliance @
- 2014 -2015 Director, R and D Quality Assurance @ ARIAD Pharmaceuticals, Inc.
- 2013 -2014 Director, Clinical Quality Assurance @
- 2012 -2013 Associate Director, Clinical Quality Assurance @
- 2004 -2012 Associate Director, Quality Assurance @
- 2003 -2004 Manager, Quality Assurance @ Anapharm
- 2002 -2003 Manager, Quality Assurance Production @ BioSignal PerkinElmer
- 2001 -2002 Associate Director, Quality Control and Technical Affairs @
- 2000 -2001 Associate Director, Quality Assurance @ Shire Pharmaceuticals
- now Sr Manager, Technical Operations @
- now Research Assistant @
Daniel Houde Education
- Université de Montréal
Certificat (Rédaction professionnelle)
2024-2028 - University of Florida
Graduate Certificate (Medical Physiology)
2020-2026 - UQAM | Université du Québec à Montréal
LL.B. (Law)
1992-1998 - UQAM | Université du Québec à Montréal
M.B.A. (Management)
1992-1994 - Université du Québec à Trois-Rivières
B.Sc. (Biochemistry)
1976-1980
Daniel Houde Skills
- Regulatory Requirements
- FDA
- 21 CFR Part 11
- GCP
- Sop
- CRO
- Regulatory Submissions
- GxP
- Regulatory Affairs
- GLP
- Computer System Validation
- CAPA
- GMP
- Biopharmaceuticals
- Pharmaceutical Industry
- Clinical Development
- Clinical Trials
- Biotechnology
- Vaccines
- Vaccine
- Infectious Diseases
- Lifesciences
- Drug Discovery
- CTMS
- Quality Assurance
- ICH-GCP
- Validation
- Pharmacovigilance
- Quality Control
- Change Control
- Drug Development
- V&V
- Oncology
- Clinical Research
- R&D
- Life Sciences
- Ich Gcp
- Good Laboratory Practice Glp
- Good Clinical Practice Gcp
- Compliance
- u.s. Food and Drug Administration Fda
- Standard Operating Procedure Sop
- Good Clinical Practice
- u.s. Food and Drug Administration
- Good Laboratory Practice
- Standard Operating Procedure
Daniel Houde Summary
- Daniel Houde, based in Terrebonne, QC, CA, is currently a Head, Clinical Quality Assurance at Seriant (formerly MHICC). Daniel Houde brings experience from previous roles at Biorasi, IQVIA Canada, Novartis and Medicago. Daniel Houde holds a 2024 - 2028 Certificat in Rédaction professionnelle @ Université de Montréal. With a robust skill set that includes Regulatory Requirements, FDA, 21 CFR Part 11, GCP, Sop and more. Daniel Houde has 2 emails on RocketReach.
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