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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
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
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
IT'SQA Associates Ltd Worldwide Audits - Clinical Study, Audits - Systems, Audits - Vendor , Computing, Good Clinical Practice (GCP), Good Computerised Systems Practice (GCSP), Good Pharmacovigilance Practice (GPVP), ISO:9001, Pharmacovigilance (PV), Quality Management Systems (QMS), Regulatory Mock Inspections, Risk Management, Standard Operating Procedures (SOPs), Training
JW Quality Consulting Limited Europe, United Kingdom, Worldwide Auditing, Audits - CMO, Audits - Company, Audits - For Cause , Audits - Process, Audits - Systems, Audits - Vendor , CAPA Management Systems, Coaching, Compliance Remediation, Due Diligence, Facility inspections, Good Distribution Practice (GDP), Good Manufacturing Practice (GMP), IMP Qualified Person, ISO:9001, Implementation, Improvement, Inspection Preparation, Inspection Support, Mentoring, Microbiology, Mock Inspections, Process, Product Specification File, QA Management, QA Systems, QP Services, Qualification and Evaluation, Quality Control (QC), Quality Management Systems (QMS), Quality Risk Management (QRM), Standard Operating Procedures (SOPs), Steriles, Support & Management, Technical Agreement, Training, cGMP
Julia Vickers Quality Services Consultancy Europe, United Kingdom, Worldwide Advice on all aspects, Auditing, Field Studies, Good Laboratory Practice (Field Studies), Good Laboratory Practice (GLP), Good Research Practice (GRP), Good control Laboratory Practice (GcLP), Inspection Preparation, QA Systems, Research, Standard Operating Procedures (SOPs), Support & Management, Training
Medwork Europe, Worldwide Auditing, Audits - CRO, Audits - Clinical Study, Audits - Company, Audits - For Cause , Audits - Investigator Site , Audits - Phase I-IV , Audits - Process, Audits - Report, Audits - Site , Audits - Sponsor , Audits - Systems, Audits - Vendor , CRO, CRO/Vendor Qualification and Evaluation, Clinical Safety, Coaching, Facility inspections, GCP Auditing, Good Clinical Laboratory Practice (GCLP), Good Distribution Practice (GDP), Good Pharmacovigilance Practice (GPVP), Implementation, Improvement, Inspection Preparation, Support and Management, Inspection Support, Inspection Support and Mentoring, Medical Devices, Mentoring, Non-Regulated Research, Pharmacovigilance (GVP), Pharmacovigilance (PV), Quality Management Systems (QMS), Standard Operating Procedures (SOPs), Support & Management, Training
Mirabilitas Ltd Worldwide Computer System Validation (CSV), Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP), Inspection Support, Non-Regulated Research, Pharmacovigilance (PV)
Omnia Quae Worldwide Archiving, Audit - Clinical Study Reports, Audit - GCLP, Audit - Protocols, Auditing, Auditing Good Pharmacovigilance Practice (GVP), Audits - First in Man, Audits - CRO, Audits - CSR, Audits - Central Laboratories and Due Diligence, Audits - Clinical Study, Audits - Company, Audits - For Cause , Audits - GCP: Investigator Site Audit, Audits - IT, Audits - Investigator Site , 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 - Systems, Audits - Vendor , CAPA Management Systems, CRO, CRO/Vendor Qualification and Evaluation, Clinical Site, Clinical trial audit plans, Computer System Validation (CSV), Computer System Validation Audits, Computerised System/Supplier Audits, Computerised Systems Audits, Computing, Data Centre Audits, Due Diligence, Electronic Data, Facility inspections, GCP Auditing, Good Clinical Practice (GCP), Good Computerised Systems Practice (GCSP), Good control Laboratory Practice (GcLP), Inspection Preparation, Mock Inspections, Preparation for agency inspections, QA Management, QA Systems, Quality Management Systems (QMS), Regulatory Inspection - Preparation & Hosting, Regulatory Mock Inspections, Site, Sponsor, Systems/Internal Process Audits, Vendor
PV Focus Worldwide Pharmacovigilance (PV)
PVCON Consulting Pvt Ltd Africa, Asia, Asia PAC, Europe, Middle East, United Kingdom, Worldwide Auditing, Audits - CRO, Audits - CSR, Audits - Company, Audits - For Cause , Audits - IT, Audits - Investigator Site , Audits - Phase I , Audits - Phase I-IV , Audits - Report, Audits - Site , Audits - Sponsor , Audits - Systems, Audits - Vendor , Clinical Safety, Computer System Validation (CSV), Computing, Contracts, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Good Distribution Practice (GDP), Good Laboratory Practice (Field Studies), Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP), ISO, ISO:19011, ISO:9000, ISO:9001, Implementation, Improvement, Information Security, Inspection Preparation, Medical Devices, Pharmacovigilance (GVP), Quality Management Systems (QMS), Quality Risk Management (QRM), Regulatory Mock Inspections, Research, Risk Management, Standard Operating Procedures (SOPs), Training
Peter Davies Associates Ltd Europe, United Kingdom, Worldwide Good Laboratory Practice (Field Studies), Good Laboratory Practice (GLP), Implementation, Research, Training
Pharma QA Consulting Ltd Europe, United Kingdom, Worldwide Good Clinical Practice (GCP)
Point Consultancy International Ltd Europe, United Kingdom, Worldwide Archiving, Auditing, Audits - CRO, Audits - CSR, Audits - Company, Audits - For Cause , Audits - Investigator Site , Audits - Phase I , Audits - Phase I-IV , Audits - Report, Audits - Site , Audits - Sponsor , Audits - Sponsor , Audits - Systems, Audits - Vendor , Good Clinical Practice (GCP), Inspection Preparation, Inspection Support, Inspection Support and Mentoring, Regulatory Mock Inspections, Standard Operating Procedures (SOPs), Support & Management
QA Insight Ltd Europe, United Kingdom, Worldwide Audits - Process, Audits - Systems, Bioequivalence/Bioavailability Studies, Good Clinical Practice (GCP), ISO:13485, ISO:14155, Mentoring, Quality Management Systems (QMS), Standard Operating Procedures (SOPs), Training
QRC Consultants Ltd Europe, United Kingdom, Worldwide Audit - GCLP, Audit - post marketing PV, Audits - CRO, Audits - Investigator Site , Audits - Vendor , Clinical trial audit plans, Clinical trial audit plans, Good Clinical Laboratory Practice (GCLP), Good Clinical Practice (GCP), Inspection Preparation, Pharmacovigilance (PV), Quality Management Systems (QMS), Training
Qualitas Europe, United Kingdom, Worldwide Good Clinical Practice (GCP)
Qualitus Europe, United Kingdom, Worldwide Good Clinical Practice (GCP), Pharmacovigilance (GVP), Standard Operating Procedures (SOPs), Training
Reumat Consulting Ltd Europe, United Kingdom, Worldwide Auditing, Good Clinical Practice (GCP), Good control Laboratory Practice (GcLP), Mentoring, Pharmacovigilance (PV), QA Staff, Training
Rigg UK Consulting Ltd - Pharmacovigilance QA Services Europe, United Kingdom, Worldwide Audit - Pharmacovigilance (PV), Gap Analysis and Process Mapping, Inspection Preparation, Pharmacovigilance (PV), Risk Planning, Training

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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.