Expert Profile
Todd Graham
Managing Partner, Delevan Street Biosciences
Todd Graham, is a masters-level bench scientist and medical technologist with a host of experience in both the clinical diagnostics and biotechnology fields. He has work for a number of start-up firms in the clinical diagnostics and biotechnology industries, as well as worked for larger firms within both industries. He has a broad level of expertise in assay development for quality control, pharmaceutical development and clinical diagnostics. His particular levels of expertises are molecular diagnostics, PCR, ELISA, quality control and training of bench level personnel in clinical diagnostics and biotechnology. He is also in the process of establishing a consultancy that assists academic labs in transitioning their research to industry by verifying and improving the quality of their work.
Trainings by Expert
Assay Validation for Clinical Diagnostics
Category:
Biotechnology
,
Laboratory Compliance
,
Testing and Validation
,
Quality and Safety
,
Laboratory
,
GLP & Other Best practices
,
Clinical Laboratory
,
Quality & Safety
,
Drugs Regulations
,
Biotech Regulations
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Life sciences QA/QC
,
Research & Development
,
Drug R & D
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
,
QA/QC
Vendor Qualification - How to Design and Implement an Efficient and Compliant Vendor Program
Category:
Drugs and Chemicals (Pharma)
,
Biotechnology
,
Documentation and IT
,
Quality and Safety
,
Supply Chain and Manufacturing
,
Quality & Safety
,
Drugs Regulations
,
Biotech Regulations
,
Audit & Inspection-Role
,
Drugs Inspections
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Life sciences QA/QC
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
,
QA/QC
Automating Assays for Clinical Diagnostics
Category:
Drugs and Chemicals (Pharma)
,
Biotechnology
,
GXP Pharmaceutical
,
Testing and Validation
,
Quality and Safety
,
Laboratory
,
Microbiology Laboratory
,
Clinical Laboratory
,
Drug Development
,
Quality & Safety
,
Technologies and Processes
,
Blood and Blood Products
,
Cellular and Gene Therapy
,
Biologics and Biosimilars
,
Life sciences QA/QC
,
Research & Development
,
Drug R & D
,
Life Sciences
,
QA/QC
How To Translate Academic and Discovery Assays Into GLP Compliant Assays
Category:
Drugs and Chemicals (Pharma)
,
Biotechnology
,
Documentation and IT
,
Quality and Safety
,
Drug Development
,
Quality & Safety
,
Technologies and Processes
,
Blood and Blood Products
,
Cellular and Gene Therapy
,
Biologics and Biosimilars
,
Documentation and Policy Management
,
Lifescience process & Procedures
,
Life sciences QA/QC
,
Research & Development
,
Drug R & D
,
Life Sciences
,
Documentation and Data Management
,
QA/QC
SOP's for Bioanalytical Methods Validation
Category:
Biotechnology
,
Laboratory Compliance
,
Testing and Validation
,
Quality and Safety
,
Laboratory
,
GLP & Other Best practices
,
Microbiology Laboratory
,
Clinical Laboratory
,
Analytical Laboratory
,
Quality & Safety
,
Biotech Regulations
,
Life sciences QA/QC
,
Life Sciences
,
Regulatory Affairs
,
QA/QC
Quality Control for Microbiological Media and Reagents
Category:
Biotechnology
,
Laboratory Compliance
,
All FDA Regulated Industry
,
Testing and Validation
,
Quality and Safety
,
Laboratory
,
Contamination Control
,
Microbiology Laboratory
,
Clinical Laboratory
,
Quality & Safety
,
Biotech Regulations
,
Audit & Inspection-Role
,
Lab Audit
,
Life sciences QA/QC
,
Research & Development
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Common FDA Regulations
,
QA/QC
Sample Quality Control for Molecular Diagnostics
Category:
Biotechnology
,
Quality and Safety
,
Laboratory
,
Clinical Laboratory
,
Quality & Safety
,
Biotech Regulations
,
Life sciences QA/QC
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
QA/QC
Vendor Qualification for Quality Services
Category:
Drugs and Chemicals (Pharma)
,
Biotechnology
,
Laboratory Compliance
,
GXP Pharmaceutical
,
Quality and Safety
,
Supply Chain and Manufacturing
,
Laboratory
,
Clinical Laboratory
,
Quality & Safety
,
Drugs Regulations
,
Biotech Regulations
,
Life sciences QA/QC
,
Research & Development
,
Drug R & D
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
QA/QC
Translating Academic Assays for GLP Use
Category:
Biotechnology
,
Laboratory
Laboratory Developed Tests: Challenges and Opportunities
Category:
Laboratory Compliance
