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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.

Name Area Of Work Areas 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
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
Ardensax QA 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
Aurelia Quality Assurance Pty Ltd Europe, United Kingdom, Worldwide Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP)
Bateman Quality Associates Ltd 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
Broadhurst-Brown QA Ltd Europe, United Kingdom, Worldwide Advice on all aspects, Auditing, Audits - CRO, Audits - CSR, Audits - Clinical Study, Audits - For Cause , Audits - Investigator Site , Audits - Phase I-IV , Audits - Process, Audits - Sponsor , Audits - Systems, Audits - Vendor , CRO/Vendor Qualification and Evaluation, GCP Auditing, Good Clinical Practice (GCP), Inspection Support, Quality Management Systems (QMS), Standard Operating Procedures (SOPs), Training
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
CM Quality Ltd 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
CMC International Europe, United Kingdom, Worldwide Good Clinical Practice (GCP), Good Laboratory Practice (GLP)
CT4 Consulting United Kingdom, Worldwide Audit - Clinical Study Reports, Clinical Overviews, Protocols, Risk Management Plans, Summary of Clinical Safety Reports
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
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
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
Dove Quality Solutions Asia PAC, Europe, United Kingdom, Worldwide Auditing, Audits - CRO, Audits - CSR, 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 Safety, 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, Standard Operating Procedures (SOPs), Training and Development
Empowerment Quality Engineering Ltd 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)
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)
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
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
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)
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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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.