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Register of Consultants

The Register of Consultants is an area of the RQA website where Quality Assurance Consultants advertise their services.

Consultants can be searched by their geographical availability for work and their area of expertise below.

Consultants are also listed alphabetically below, simply click the Consultancy name to view further details.

To join the Register please email advertising@therqa.com 

Disclaimer

Please note that the consultants listed are not endorsed by the RQA. This is an ADVERTISING FEATURE and does not constitute a comprehensive list of QA consultants.

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Name

Area of Work

Area of Expertise

  • Europe, United Kingdom, Worldwide
    Audits - Clinical Study, Audits - Systems, Audits - Vendor , Due Diligence, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Computerised Systems Practice (GCSP), Good Distribution Practice (GDP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Mentoring, Pharmacovigilance (GVP), Quality Management Systems (QMS), Regulatory Mock Inspections, Risk Management, Standard Operating Procedures (SOPs), Training
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  • Europe, United Kingdom, Worldwide
    Audits - For Cause , Audits - Report & Data, Audits - Vendor , Facility inspections, Good Clinical Laboratory Practice (GCLP), Good Laboratory Practice (GLP), Regulatory Inspection - Preparation & Hosting
    show more +
  • Worldwide
    Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), ISO:15189, ISO:17025
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  • United Kingdom, Worldwide
    Computing, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GPVP)
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  • Europe, United Kingdom, Worldwide
    Audits - CRO, Audits - Facility Inspection, Field Studies, Audits - For Cause , Audits - Report & Data, Audits - Sponsor , Audits - Systems, Good Clinical Practice (Veterinary), Good Laboratory Practice (Field Studies), Good Laboratory Practice (GLP), Good Research Practice (GRP), Non-Regulated Research, Regulatory Inspection - Preparation & Hosting, Regulatory Mock Inspections, Research, Training
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  • Europe, United Kingdom, Worldwide
    Advice on all aspects, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Laboratory Practice (Field Studies), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Quality Management Systems (QMS), Risk-based audit programmes, Training
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  • Europe, United Kingdom, Worldwide
    Archiving, Audit - Clinical Study Reports, Audits - First in Man, Audits - Central Laboratories and Due Diligence, Audits - Company, Audits - CRO, Audits - CSR, Audits - For Cause , Audits - Investigator Site , Audits - IT, Audits - Phase I-IV , Audits - Site Management Organisations, Audits - Sponsor Oversight, Audits - Systems, Audits - Vendor , Clinical Safety, Clinical Site, Computer System Validation (CSV), Computing, Contracts, Gap Analysis and Process Mapping, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Distribution Practice (GDP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GPVP), Healthy volunteers, In-vitro diagnostic (IVD) devices, Information Security, Inspection Preparation, ISO: 23640, ISO: 31000, ISO: 9001 Implementation, ISO: 9004, ISO:13485, ISO:14155, ISO:15189, ISO:17025, ISO:19011, ISO:9000, ISO:9001, Medical Devices, Paediatrics, Quality Improvement, Quality Management Systems (QMS), Quality Risk Management (QRM), Regulatory Affairs, Regulatory Inspection - Preparation & Hosting, Standard Operating Procedures (SOPs), Technical Agreement, Training
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  • Europe, United Kingdom, Worldwide
    Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Distribution Practice (GDP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), ISO: 14000, ISO:17025, ISO:9000
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  • Europe, United Kingdom, Worldwide
    Auditing, Audits - Company, Audits - CRO, Audits - For Cause , Audits - Investigator Site , Audits - Process, Audits - Systems, Audits - Vendor , CAPA Management Systems, Clinical trial audit plans, Coaching, CRO, Data Integrity, Due Diligence, GCP Auditing, Mock Inspections, Quality Agreements, Quality Management Systems (QMS), Quality Risk Management (QRM), Regulatory Inspection - Preparation & Hosting, Support & Management
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  • Europe, United Kingdom, Worldwide
    Auditing, Audits - Company, Audits - CRO, Audits - For Cause , Audits - Investigator Site , Audits - Phase I-IV , Audits - Process, Audits - Systems, Clinical trial audit plans, Coaching, Compliance Remediation, CRO, CRO/Vendor Qualification and Evaluation, Data Integrity, Due Diligence, GCP Auditing, Good Clinical Practice (GCP), Implementation, Improvement, Inspection Preparation, Support and Management, Mock Inspections, Phase 1 facilities, Process, QA Management, QA Systems, Quality Agreements, Quality by Design (QbD), Quality Management Systems (QMS), Quality Risk Management (QRM), Quality, Process and Technical Training, Regulatory Inspection - Preparation & Hosting, Regulatory Mock Inspections, Risk Management, Risk-based audit programmes, Training and Development, Vendor
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  • Asia PAC, Europe, United Kingdom, Worldwide
    Auditing, Audits - Company, Audits - CRO, Audits - For Cause , Audits - Investigator Site , Audits - Phase I-IV , Audits - Process, Audits - Systems, Audits - Vendor , CAPA Management Systems, Clinical trial audit plans, Coaching, Compliance Remediation, CRO, CRO/Vendor Qualification and Evaluation, Data Integrity, Due Diligence, GCP Auditing, Good Clinical Practice (GCP), Implementation, Improvement, Inspection Preparation, Support and Management, Mock Inspections, Phase 1 facilities, Process, QA Management, QA Systems, Quality Agreements, Quality by Design (QbD), Quality Management Systems (QMS), Quality Risk Management (QRM), Quality, Process and Technical Training, Regulatory Inspection - Preparation & Hosting, Regulatory Mock Inspections, Risk Management, Risk-based audit programmes, Training and Development
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  • Europe, United Kingdom, Worldwide
    21 CFR Part11, Audits - IT, Audits - Systems, Audits - Vendor , Bespoke CSV Training, Computer System Validation (CSV), Computer System Validation Audits, Computerised System/Supplier Audits, Computerised Systems (Process and Technical), Computerised Systems Consultation, Computerised Systems/Supplier Selection, Data Centre Audits, Data Integrity, Good Clinical Practice (GCP), Good Computerised Systems Practice (GCSP), Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GPVP), GxP Assessments, ISO: 27001, ISO: 31000, ISO: 90003, ISO: 9004, ISO:13485, ISO:19011, ISO:9000, ISO:9001, IT Audit Training, IT Supplier Contracts, IT Systems Coaching, IT Systems Integrations Verification and Validation, Medical Devices, QA Management, QA Staff, Quality Improvement, Quality Management Systems (QMS), Quality Management Systems (QMS), Quality Risk Management (QRM), Quality, Process and Technical Training, Quality, Process and Technical Training, Risk Management, SDLC Training, Standard Operating Procedures (SOPs), Technical Contracts and Agreements
    show more +
  • Worldwide
    21 CFR Part11, Advice on all aspects, Audit - Clinical Study Reports, Audit - GCLP, Audit - Pharmacovigilance (PV), Audit - post marketing PV, Audit - Protocols, Auditing, Auditing Good Pharmacovigilance Practice (GVP), Audits - First in Man, Audits - Central Laboratories and Due Diligence, Audits - Clinical Study, Audits - CMO, Audits - Company, Audits - CRO, Audits - CSR, Audits - Data Management and Statistics, Audits - Facility Inspection, Field Studies, Audits - For Cause , Audits - GCP: Investigator Site Audit, Audits - Investigator Site , Audits - IT, Audits - Phase I , Audits - Phase I-IV , Audits - Process, Audits - Report, Audits - Report & Data, Audits - Site , Audits - Site Management, Audits - Site Management Organisations, Audits - Sponsor , Audits - Sponsor Oversight, Audits - Study and Process Based, Audits - Systems, Audits - Vendor , Bespoke CSV Training, Clinical trial audit plans, Compliance Advice, Compliance Remediation, Computer System Validation (CSV), Computer System Validation Audits, Computerised System/Supplier Audits, Computerised Systems (Process and Technical), Computerised Systems Audits, Computerised Systems Consultation, Computerised Systems/Supplier Selection, CRO/Vendor Qualification and Evaluation, Data Centre Audits, Data Integrity, Due Diligence, Electronic Data, Ex-FDA Inspector Consulting and Response Support, Facility inspections, Gap Analysis, GCP Auditing, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Clinical Practice (Veterinary), Good Computerised Systems Practice (GCSP), Good control Laboratory Practice (GcLP), Good Distribution Practice (GDP), Good Laboratory Practice (Field Studies), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GPVP), Good Research Practice (GRP), GxP Assessments, Inspection Hosting, Inspection Hosting and Preparation, Inspection Preparation, Inspection Preparation and Training, Inspection Preparation, Support and Management, Inspection Support, Inspection Support and Mentoring, ISO, IT Audit Training, IT Supplier Contracts, IT Systems Integrations Verification and Validation, Medical Devices, Mock Inspections, Pharmacovigilance (GVP), Pharmacovigilance (PV), Pharmacovigilance: systems/internal process audits, Preparation for agency inspections, QA Management, QA Staff, QA Systems, QP Services, Qualification and Evaluation, Quality Agreements, Quality Improvement, Quality Management Systems (QMS), Quality Risk Management (QRM), Quality, Process and Technical Training, Regulated IT Project Management/Delivery, Regulatory Affairs, Regulatory Inspection - Preparation & Hosting, Regulatory Inspection Support, Regulatory Mock Inspections, Regulatory Responses, Risk Management, Risk Management Plans, Risk Planning, Risk-based audit programmes, SDLC Training, SOP Writing, Standard Operating Procedures (SOPs), Support & Management, Systems/Internal Process Audits, Training, Training and Development, Vendor
    show more +
  • Asia, Europe, United Kingdom, Worldwide
    Auditing, Audits - Clinical Study, GAMP 5 (CSV), Good Clinical Practice (GCP), Good control Laboratory Practice (GcLP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), ISO:13485, ISO:14155, ISO:9001, Vendor
    show more +
  • Europe, United Kingdom, Worldwide
    Audit - GCLP, Audit - Pharmacovigilance (PV), Auditing, Auditing Good Pharmacovigilance Practice (GVP), Audits - Systems, Audits - Vendor , Gap Analysis, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Distribution Practice (GDP), Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GPVP), Good Pharmacovigilance Practice (GPVP), Good Research Practice (GRP), Inspection Preparation, Inspection Preparation and Training, Pharmacovigilance (PV), Training
    show more +
  • Europe, United Kingdom, Worldwide
    21 CFR Part11, Business Analysis, Computer System Validation (CSV), Data Integrity, Electronic Data, Good Clinical Laboratory Practice (GCLP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), ISO:13485, ISO:17025, LIMS, Regulated IT Project Management/Delivery
    show more +
  • Europe, United Kingdom, Worldwide
    Field Studies, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), ISO:17025, ISO:9001, Non-Regulated Research
    show more +
  • Asia, Asia PAC, Australasia
    Audit - GCLP, Audits - CRO, Audits - For Cause , Audits - Investigator Site , Audits - Phase I-IV , Audits - Vendor , Clinical Process Review & Gap Analysis, Clinical QA Auditor Training, GCP & Audit Preparation Training, GCP & Gap Analysis, GCP Pharmacy Audits, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Quality Focused Site Visits
    show more +
  • Worldwide
    Audits - Report & Data, Audits - Study and Process Based, Audits - Vendor , Facility inspections, Good Clinical Laboratory Practice (GCLP), Good Laboratory Practice (GLP), Inspection Hosting and Preparation, Non-Regulated Research
    show more +
  • Europe, United Kingdom, Worldwide
    Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GPVP), ISO: 14001, ISO: 18001, ISO: 27001, ISO: 9001 Implementation
    show more +
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