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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.

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Name

Area of Work

Area of Expertise

  • ADAMAS Consulting Ltd
    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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  • AF International Consultancy
    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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  • Aurelia Quality Assurance Pty Ltd
    Australasia, Europe, United Kingdom, Worldwide
    Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP)
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  • Buckingham QA Consultancy
    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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  • CMC International
    Europe, United Kingdom, Worldwide
    Good Clinical Practice (GCP), Good Laboratory Practice (GLP)
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  • Chapman QA
    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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  • ClinPark QA Ltd
    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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  • Clinical Quality Assurance Company
    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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  • Digital Quality Associates
    Europe, United Kingdom, Worldwide
    Auditing, Audits - CRO, Audits - Company, Audits - For Cause , Audits - Investigator Site , Audits - Phase I-IV , Audits - Process, Audits - 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, Vendor
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  • Dove Quality Solutions
    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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  • Emas Pharma
    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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  • Empowerment Quality Engineering Ltd
    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
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  • FDA Quality and Regulatory Consultants, LLC (FDAQRC)
    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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  • Formpipe Life Science
    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
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  • GXP Engaged Auditing Services
    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
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  • Greatspur Clinical Development Ltd
    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
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  • Handy Consulting Ltd
    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), Good Research Practice (GRP), Pharmacovigilance (PV)
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  • Hazel McMeekin SciVal Ltd
    Europe, United Kingdom, Worldwide
    21 CFR Part11, Business Analysis, Computer System Validation (CSV), Computing, Data Integrity, Electronic Data, Electronic Data, Good Clinical Laboratory Practice (GCLP), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), ISO:13485, Regulated IT Project Management/Delivery
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  • Headway Quality Evolution
    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
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  • IntuVigilance Ltd
    Europe, United Kingdom, Worldwide
    Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GPVP), ISO: 14001, ISO: 18001, ISO: 27001, ISO: 9001 Implementation
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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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