Our public member list
AVC has much more members. Here we just list those members who wants to listed public.
C/ Ausias March 1, 4a planta D01 Office: +34-93-675-8015
08195 Sant Cugat del Vallès, Barcelona
Regulatory affairs, EU regulations & EFSA guidelines, strategy, food & feed additive registration, technical writing, novel food registration, nutrition & health claims, training, event chairing & conference presentations.
Via della Divisione Torino 113
F: +39 338 671 53 14
Registration, IT, Regulatory Affairs, Clinical Trials, Safety
6024 6th Line East
N08 18D Ariss Ontario
Consulting in resarch imaging - all species and all modalities, animal welfare regulations Canada and US
Pharmacovigilance, Regulatory Affairs, Quality, Medical writing, MUMS, GMP, Medical Devices, Animal Welfare
Consulting regulatory strategy, market access to Russian/EAEU and African (UEMOA) markets. Market analysis, establishing partnerships and distribution network. Registration of veterinary products and feed additives in Russia/EAEU (full cycle from dossier assessment to obtaining registration certificate). Preparation to Russian GMP inspection. In-house seminars and training of regulatory aspects in Russia/EAEU: Registration of VMPs, Registration of feed additives, Updated regulations for feed and feed additives in EAEU, GMP inspection
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46-54 High Street
Veterinary Medicines & Biologicals Regulatory Affairs, Regulatory Intelligence, Expert Reports (Efficacy, Safety), Pharmacovigilance, Technical Support and Training.
F: +49 51 66 931 9829
Safety and Efficacy trials according to GLP/VICH-GCP for veterinary medicinal products, biologicals, feed additives (own GLP compliant testing facility), pharmacology / toxicology
EMA, FDA: nonclinical product development of human therapeutics (biologicals, small molocueles, gene and cell therapy) regulatory toxicology of human therapeutics Expert reports: safety evaluations, risk mitigation strategies nonclinical program design nonclinical MA dossiers GLP monitoring
3-10-9 Oyamadai, Setagaya-ku,
Lyalin pereulok, 5/1,b.3
CT2 7RL Centerbury, Kent
M: +44 703 458 6969
Bank Barn, How Mill
CA8 9JY Brampton
M: +44 77 99 88 25 25
F: +44 845 123 28 89
Clinical Trials: data management, statistics, QA, Electronic Data Capture & electronic Quality of Life. Vet. Medicine R&D and complete Regulatory Affairs in both VMPs & Biologicals. DACS, QA, Part 2 (CMC), Training, Databases, Toxicology, PV.
The Round House, The Friary, Old Windsor
SL4 2NR Berkshire
F: +44 1753 831 886
Retired Honorary Member
Private Bag West Armidale
2350 New South Wales
F: +61 2 6772 5184
Pen and field Trials, efficacy, tolerance, safety, residue and pharmacokinetic studies in production animals - cattle (incl. dairy), sheep, pigs, goats, poultry - and horses. GLP compliant and GCP studies
68 Macrae Road, Eden Office Park, Ham Green
BS20 0DD Bristol
Regulatory Affairs VMPs and Biologicals, Project Management, Pre-clinical & Clinical development, Expert Reports & DACS (Quality, Safety & Efficacy), Environmental and User Safety Risk Assessments, Pharmacovigilance
F: +34 976 312753
Marketing, Licence/Distribution Agreements, Interim Management, Areas: Feed Additives, Animal Production, Animal Health
122 Allan St. Port Perry
L9L 1E4 Ontario
Product development; project management; GLP/GCP study design and monitoring; quality systems design and implementation; and business development.
M: +49 171 7218954
F: +49 89 58 00 82 77 77
European and global animal health product development incl. all aspects: Project management, regulatory affairs, safety and efficacy studies incl. data management & statistics, Electronic Data Capture, quality assurance for Veterinary Medicinal Products, Feed Additives and other biological and biotechnical products incl. novel therapies. Import, release of VMPs EU GMP compliant. Studies to VICH GCP or GLP. All activities in a quality management system certified to ISO 9001.
Veterinary Drug Registration, EMA procedures, Oral Hearings, Referrals, MUMS, dossier content and List of Questions. VICH global development. DACS, safety & efficacy
Veterinary medicines registration, Part III/IV expert reports, efficacy, tolerance, safety, residue and pharmacokinetic studies, statistical analyses, PK/PD modelling, GCP (VICH) clinical trials.
45 St. Barnabas Road
CB1 2BX Cambridge
Market Dynamics Studies, Veterinary Medicines Registration, Feed Additives Registration, Management of Biotechnology and other Innovations in Animal Health
Valby Overdrev 6
M: +45 40 46 54 60
Regulatory Affairs, Pharmacovigilance, Clinical Trials (GCP), Scientific writing & translations
Devon House, 109 Mayfield Road, Ashbourne,
DE6 1AS Derbyshire
Veterinary medicine R&D: project managing and/or monitoring for Clinical Trials (VICH+GCP), TASS (GL43+GLP), Auditing (GLP and GCP), Training (GCP) and Technical Writing.
CB24 5PW OverCambridge
M: +44 7522 860021
Veterinary Medicine R+D from screening to authorization, Clinical Development, Project Management, Regulatory affairs, Expert reports (efficacy)
F: +34 97 52 14 193
Veterinary Clinical Sciences - Clinical Trials, Veterinary Medicines R&D, Veterinary Medicines Registration, Biostatistics
FK8 3HL Kippen
Research - developing scientifically robust structured questionnaire instruments to measure pain and health related quality of life in non verbal species
34160 Saint Geniès de Mourgues
F: +33 467 86 08 86
Pharmacology-Toxicology, Veterinary Clinical Sciences, Veterinary Medicines R&D, Veterinary Medicines/Feed Additive Registration
YO62 4LW Cawton, York
Scientific & Clinical expertise for Product Development, Specialist in Pharmaceuticals, pharmacology, efficacy, safety, Animal Production
20280 Hondarriba (Gipuzkoa)
M: +34 659 939 586
European Clinical Trials in companion animals and livestock: proof-of concept, pilot and pivotal (VICH-GCP) studies. Clinical development, monitoring, data management (EDC), quality assurance, statistics and regulatory affairs
M: +49 173 200 59 42
F: +49 40 380178 54668
Pharmacology/Toxicology. Veterinary Clinical sciences - Clinical Trials, Laboratory Investigations. Veterinary Drug R&D. Veterinary Drug Registration
5 allée des amaryllis
F-69290 Saint Genis les Ollières
F: +33 956158825
Pharmacovigilance expert including QPPV services, Veterinary Drug Registration (non-clinical & Clinical)
vaccine production, QC, R&D, product manager, technical assistance and regulatory affairs. Support for technical and regulatory affairs for new and existing business. Support for development of new businesses in Brazil for global players.
4 Thorny Way, Highfields Caldecote
CB23 7ZE Cambridge
Clinical trials, Veterinary drug D&D, Veterinary drug registration, Pharmacovigilance, Scientific writing, Marketing and technical support
rue G. Charlier 11/33
Activities: Feed additives/Feed materials registration, Veterinary medicines R&D. Lobbying for AH.
5688JW Spoordonk (Oirschot)
Veterinary RA &RD including: - Complete Pharmaceutical Development (Part 2) - GCP trials (Cats, dogs, horses) - Expert reports Part 2, 3 and 4 - Drug Registration