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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, download a booking form here.

Filter Consultants

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
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  • Europe, United Kingdom, Worldwide
    Audit - GCLP, Auditing, Audits - CRO, Audits - CSR, Audits - Clinical Study, Audits - For Cause , Audits - Investigator Site , Audits - Phase I , Audits - Phase I-IV , Audits - Process, Audits - Report, Audits - Report & Data, Audits - Site , Audits - Sponsor , Audits - Systems, Audits - Vendor , Bioequivalence/Bioavailability Studies, CAPA Management Systems, CRO/Vendor Qualification and Evaluation, Clinical Site and Phase I Unit Good Manufacturing Practice (GMP), GCP Auditing, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), IMP Qualified Person, ISO:15189, ISO:17025, ISO:9001, Phase 1 facilities, Quality Management Systems (QMS), Regulatory Inspection Support, Standard Operating Procedures (SOPs), Vendor, cGMP
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  • Europe, United Kingdom, Worldwide
    Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP)
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  • Europe, United Kingdom, Worldwide
    Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Distribution Practice (GDP), Good Manufacturing Practice (GMP), Good control Laboratory Practice (GcLP), HFEA Code of Practice, ISO:17025, ISO:9001, cGMP
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  • Europe, United Kingdom, Worldwide
    Advice on all aspects, Audit - Pharmacovigilance (PV), Audit - Protocols, Auditing, Auditing, Audits - CMO, Audits - CRO, Audits - CRO, Audits - CSR, Audits - CSR, Audits - Clinical Study, Audits - Clinical Study, Audits - For Cause , Audits - For Cause , Audits - Investigator Site , Audits - Investigator Site , Audits - Phase I-IV , Audits - Phase I-IV , Audits - Process, Audits - Process, Audits - Sponsor , Audits - Sponsor , Audits - Systems, Audits - Systems, Audits - Vendor , Audits - Vendor , CRO/Vendor Qualification and Evaluation, CRO/Vendor Qualification and Evaluation, GCP Auditing, GCP Auditing, Good Clinical Practice (GCP), Good Clinical Practice (GCP), Inspection Preparation and Training, Inspection Support, Inspection Support, Quality Management Systems (QMS), Quality Management Systems (QMS), Quality Risk Management (QRM), Standard Operating Procedures (SOPs), Training, Training
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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
    Audits - GCP: Investigator Site Audit, Audits - Vendor , Compliance Advice, Computing, Due Diligence, Good Clinical Practice (GCP), Marketing Partners, Mentoring, Pharmacovigilance (PV), Pharmacovigilance: systems/internal process audits, Quality Management Systems (QMS), Regulatory Mock Inspections, Risk Management, Standard Operating Procedures (SOPs), Systems/Internal Process Audits, Training, Vendor
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  • Europe, United Kingdom, Worldwide
    Good Clinical Practice (GCP), Good Laboratory Practice (GLP)
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  • United Kingdom, Worldwide
    Audit - Clinical Study Reports, Clinical Overviews, Protocols, Risk Management Plans, Summary of Clinical Safety Reports
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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
    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
    Archiving, Audit - Clinical Study Reports, Audits - First in Man, Audits - CRO, Audits - CSR, Audits - Central Laboratories and Due Diligence, Audits - Company, Audits - For Cause , Audits - IT, Audits - Investigator Site , 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, ISO: 23640, ISO: 31000, ISO: 9001 Implementation, ISO: 9004, ISO:13485, ISO:14155, ISO:15189, ISO:17025, ISO:19011, ISO:9000, ISO:9001, In-vitro diagnostic (IVD) devices, Information Security, Inspection Preparation, 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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  • Asia PAC, Europe, United Kingdom, Worldwide
    Auditing, Audits - CRO, Audits - Company, Audits - For Cause , Audits - Investigator Site , Audits - Phase I-IV , Audits - Process, Audits - Systems, Audits - Vendor , CAPA Management Systems, CRO, CRO/Vendor Qualification and Evaluation, Clinical trial audit plans, Coaching, Compliance Remediation, 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 Management Systems (QMS), Quality Risk Management (QRM), Quality by Design (QbD), 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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  • 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
    Computer System Validation (CSV), Computerised System/Supplier Audits, Computerised Systems (Process and Technical), Computerised Systems Consultation, Computerised Systems/Supplier Selection, Data Centre Audits, Good Clinical Practice (GCP), Good Manufacturing Practice (GMP), GxP Assessments, ISO: 27001, ISO: 90003, ISO: 9004, ISO:19011, ISO:9000, ISO:9001, Quality Management Systems (QMS), Quality, Process and Technical Training, Standard Operating Procedures (SOPs)
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  • Worldwide
    Computing, Ex-FDA Inspector Consulting and Response Support, Field Studies, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Non-Regulated Research, Pharmacovigilance (PV)
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  • Europe, United Kingdom, Worldwide
    Auditing, Compliance Remediation, Computer System Validation (CSV), Good Clinical Practice (GCP), Good Distribution Practice (GDP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Inspection Preparation, Quality Management Systems (QMS), Regulatory, Standard Operating Procedures (SOPs), Training
    show more +
  • Worldwide
    Computing, Field Studies, Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), Good Pharmacovigilance Practice (GPVP), Good control Laboratory Practice (GcLP), Non-Regulated Research
    show more +
  • Europe, United Kingdom
    Auditing, Audits - CRO, Audits - CSR, Audits - Clinical Study, Audits - Company, Audits - For Cause , Audits - Investigator Site , Audits - Phase I , Audits - Phase I-IV , Audits - Process, Audits - Report, Audits - Site , Audits - Sponsor , Audits - Systems, Audits - Vendor , Clinical Safety, Clinical Site and Phase I Unit Good Manufacturing Practice (GMP), Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GPVP), ISO:14155, Implementation, Improvement, Inspection Preparation, Inspection Support, Pharmacovigilance (GVP), Quality Management Systems (QMS), Regulatory Inspection Support, Regulatory Mock Inspections, Standard Operating Procedures (SOPs), Training
    show more +
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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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