Expert Profile
Carlos Rodriguez Garcia
Director of Operations Support, ZS Pharma
Carlos A. Rodriguez-Garcia, PhD, ASQ CSSGB, CBA is president of BioMed Pharma Consulting, LLC, an independent consulting firm providing services in quality management systems to the pharmaceutical and medical industries. Mr. Rodriguez-Garcia has over 15 years of experience in the regulated industry, the vast majority in quality management, encompassing a wide scope of products and processes: plastics, parenterals and aseptic processes. His experience includes conducting and approving CAPA investigations as well as training investigators in root cause analysis techniques and proper documentation of CAPA investigations to comply with FDA and EU requirements.
Trainings by Expert
CAPA Investigations - Tools for a Compliant and Effective Investigation Process
Category:
Medical Devices
,
Biotechnology
,
Laboratory Compliance
,
All FDA Regulated Industry
,
Documentation and IT
,
Quality and Safety
,
QMS, ISO 13485, CAPA
,
Supply Chain and Manufacturing
,
Laboratory
,
Quality & Safety
,
Drugs Regulations
,
Biotech Regulations
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Life sciences QA/QC
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
,
QA/QC
Technology Transfer and Validation for Medical Devices and Pharmaceuticals: The Link between Development, Validation and Commercial Production
Category:
Drugs and Chemicals (Pharma)
,
Medical Devices
,
All FDA Regulated Industry
,
GXP Pharmaceutical
,
GXP Medical Devices
,
FDA Validation
,
Testing and Validation
,
Quality and Safety
,
QMS, ISO 13485, CAPA
,
Supply Chain and Manufacturing
,
Drug Development
,
Life sciences QA/QC
,
Research & Development
,
Drug R & D
,
Device R & D
,
Life Sciences
,
QA/QC
