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
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
158-0086 Setagaya-ku, Tokyo
Regulatory consulting : registration of animal medicines, veterinary medical devices, in vitro diagnostic kits and feed addtives in Japan Regulatory affairs: Member of VICH Pharmacovigilance Expert Working Group and Electric File Transfer EWG Designated Marketing Authorization Holder (D-MAH) for Foreign AH manufacturers, Market Research, Strategic Planning, and Lecturer & Writer
ul. Bol'shaya Kosinskaya, office 332
Regulatory advice (including in-house & written) on the circulation of veterinary drugs and vaccines, feed additives in the Russian Federation and the EEU Strategic advice on registration, preclinical and clinical studies, GMP inspections ( the legislation of the RF and the EEU)
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
PO Box 865 Armidale, NSW
Specialist interest in pathobiology and in particular parasitic diseases of production animals. Strategic advice on design and conduct of clinical studies, particularly for conduct in Australia or New Zealand
68 Macrae Road, Eden Office Park, Ham Green
BS20 0DD Bristol
Regulatory Affairs VMPs and Biologicals, Feed Additives, Project Management, Pre-clinical & Clinical development, Expert Reports & DACS (Quality, Safety & Efficacy), MRLs, Toxicology, Environmental and User Safety Risk Assessments, Pharmacovigilance, Chemistry Manufacture Control (CMC), GMP.
Park Farm Buildings Park Lane
GL15 6QX St Briavels
Preclinical and Clinical Studies: data management, statistics, QA, Veterinary medicines, feed additives, diagnostics and biological products. Project management, safety and efficacy studies incl. data management & statistics, for Veterinary Medicinal Products, Feed Additives, diagnostics and other biological and biotechnical products incl. novel therapies. Studies to VICH GCP or GLP. Expert reports or DACS. Scientific writing.
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
We provide assistance and guidance in a wide range of services, with a focus on: -Veterinary product development -Project management -GLP/GCP study design and monitoring -Quality systems design and implementation -Opinion leader recruitment -Business development -US/Canadian agent services for regulatory submissions
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
Regulatory affairs: biomaterials; strategies for establishing novel products. Business strategies: business-to-business links for strategic collaborations, product-finding and in/out-licencing in Europe and Europe to China, Europe to USA. Biotechnology, circular bioeconomy issues (wastes-to-products). Market analysis and routes-to-market for novel products. Chairing and facilitating workshops and seminars.
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.
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
42 chemin des Olivettes
34160 Saint Genies des Mourgues
Study design and management for Veterinary Medicines/Feed Additive Registration Mathematical models in Toxicology, Pharmacodynamics and Pharmacokinetics (PK/PD), Benefit/Risk Assessment (Target Animals, Consumers, Users, Environment)
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 Many thanks to Dr Rudi Scherkl, who will act as AVC representative in future EC/EFSA Bee Health Meetings.
5 allée des amaryllis
F-69290 Saint Genis les Ollières
F: +33 956158825
EU Drug Registration,new Marketing Authorisation Application dossiers - Variations - dossier preparation & submission - safety & efficacy Good distribution practices - Responsible Person GDP Pharmacovigilance: EU-QPPV - LCP (Local Contact Person for Pharmacovigilance) - PV Audits - PSURs - PSMF - post-marketing surveillance
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
Previous expertise in EU regulatory affairs vet.medicines and feed additives Many thanks to Dr Bill Vandaele for attending EFSA Bee Health Meetings as the selected AVC Bee Expert until October 2019, & for his continued support to AVC
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