Our public member list

AVC has much more members. Here we just list those members who wants to listed public.

Name

Address

State

Contactdata

Dr. McCartney, Elinor
(President)
Pen & Tec Consulting, S.L
C/ Ausias March 1, 4a planta D01 Office: +34-93-675-8015
08195 Sant Cugat del Vallès, Barcelona
ES
T: +34-93-675-8002
M: +34-699-053-898
F: +34-93-675-8016
http://pentec-consulting.eu/
elinor@pentec-consulting.eu

Regulatory affairs, EU regulations & EFSA guidelines, strategy, food & feed additive registration, technical writing, novel food registration, nutrition & health claims, training, event chairing & conference presentations.
Dr. med. vet. Agostini, Alessandro
(Senior-President)
G.A.B.A. s.r.l.
Via della Divisione Torino 113
00143 Roma
IT
T: +39 6 811 075 20 - 22
F: +39 338 671 53 14
alessandro@gabaregulatory.com

Registration, IT, Regulatory Affairs, Clinical Trials, Safety
Dobson, Howard
(Vice-president)
Imaging Research Consultant
6024 6th Line East
N08 18D Ariss Ontario
Canada

Consulting in resarch imaging - all species and all modalities, animal welfare regulations Canada and US
Dr. Ishimbaeva Ivanov, Rimma
(Treasurer)
989 bis Route de Notre Dame Cidex 49
06330 Roquefort-les-Pins
FR
T: +33695643737
rimmaichi@gmail.com

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
Velletti, Jörg
(Webmaster)
Würmtalstr. 161
81375 München
DE
T: +49 89 44 9000 73
M: ++49 177 30 9 1960
http://www.velletti.de
webmaster@avc-eu.de

If you have questions concerning the webpage, feel free to contact me.
Cooper, Paul
Assentra Ltd
46-54 High Street
Ingatestone, Essex
UK
T: +44 1277 353451
M: +44 7849 438284
http://www.assentra.com/
paul.cooper@assentra.com

Veterinary Medicines & Biologicals Regulatory Affairs, Regulatory Intelligence, Expert Reports (Efficacy, Safety), Pharmacovigilance, Technical Support and Training.
Dr. Schmidt, Holger
BioMedVet Research GmbH
Suedkampen 31
29664 Walsrode
Germany
T: +49 51 66 931 980
F: +49 51 66 931 9829
h.schmidt@biomedvet.de

Safety and Efficacy trials according to GLP/VICH-GCP for veterinary medicinal products, biologicals, feed additives (own GLP compliant testing facility), pharmacology / toxicology
DVM, MS Ujimasa, Yuki
AHRMS, Inc.
3-10-9 Oyamadai,
158-0086 Setagaya-ku, Tokyo
Japan

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
Kiryukhina, Nina
VetRegister, LlC
ul. Bol'shaya Kosinskaya, office 332
105062 Moscow
RU
T: +7-495-700-7054
M: +7 917 555 0431
http://vetregistr.com/
genman@vetregistr.com

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)
O'Rourke, Declan
Ortec Consultancy
Friaryway 1
CT2 7RL Centerbury, Kent
UK
T: +44 1227 764635
M: +44 703 458 6969
http://ortec-consultancy.co.uk
dorourke@ortec-consultancy.co.uk

Braidwood, Julian
Triveritas
Bank Barn, How Mill
CA8 9JY Brampton
UK
T: + 44 845 123 28 88
M: +44 77 99 88 25 25
F: +44 845 123 28 89
http://www.triveritas.com/
julian.braidwood@triveritas.com
Skype: jcb.triveritas

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.
Burch, David G. S.
Octagon Services
The Round House, The Friary, Old Windsor
SL4 2NR Berkshire
UK
T: +44 1753 831 886
F: +44 1753 831 886
D.Burch@Octagon-Services.co.uk

Retired Honorary Member
Chick, Bruce
Bruce Chick Consulting
Burgess Street
PO Box 865 Armidale, NSW
AU
T: +61427007403
bruce@brucechick.com

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
Edwards, Helen
Cyton Biosciences Ltd
68 Macrae Road, Eden Office Park, Ham Green
BS20 0DD Bristol
UK
T: +44 (0) 117 973 9244
HEdwards@cyton.com

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.
Dr Fisher, Maggie
Ridgeway Research Ltd
Park Farm Buildings Park Lane
GL15 6QX St Briavels
UK

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.
Garcia Aranda, Oscar
Paseo de la Gran Vía, primero Izda.
50.006 Zaragoza
ES
T: + 34 685 328512
F: +34 976 312753
o.garcia@colvet.es

Marketing, Licence/Distribution Agreements, Interim Management. Areas: Feed Additives, Animal Production, Animal Health
Hare, Jonathan
Telemark Veterinary Consulting Inc.
122 Allan St. Port Perry
L9L 1E4 Ontario
CA

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
Hellmann, Klaus
KLIFOVET AG
Geyerspergerstrasse 27
80689 München
DE
T: +49 89 58 00 820
M: +49 171 7218954
F: +49 89 58 00 82 77 77
http://www.klifovet.com/
klaus.hellmann@klifovet.com
Skype: Dr.Klaus.Hellmann

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.
Holm, Anja E. H.
Central VetPharma Consultancy
Hauchsvej 7
4180 Soroe
DK

Veterinary Drug Registration, EMA procedures, Oral Hearings, Referrals, MUMS, dossier content and List of Questions. VICH global development. DACS, safety & efficacy
Liège, Philippe
ANISTEME Biosciences
Saint-Christol
34400 Entre-Vignes
FR
T: +33 467 67 24 52
M: +33 683 27 83 51
http://www.anisteme.com/
pliege@anisteme.net

Veterinary medicines registration, Part III/IV expert reports, efficacy, tolerance, safety, residue and pharmacokinetic studies, statistical analyses, PK/PD modelling, GCP (VICH) clinical trials.
Lloyd-Evans, Meredith
BIOBRIDGE Ltd.
45 St. Barnabas Road
CB1 2BX Cambridge
UK

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.
Manniche, Niels-Erik
PHARManniche
Valby Overdrev 6
3200 Helsinge
DK
T: +45 48 39 48 61
M: +45 40 46 54 60
niels-erik@manniche.eu

Regulatory Affairs, Pharmacovigilance, Clinical Trials (GCP), Scientific writing & translations
Nissen, Anne-Kirstine
AK Research & Development Ltd
Devon House, 109 Mayfield Road, Ashbourne,
DE6 1AS Derbyshire
UK

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.
Pobel, Thierry
C/.Los Betetas, 12 - 4° D
42002 Soria
ES
T: +34 97 52 14 876
F: +34 97 52 14 193
thierry.pobel@tpcbiomed.com

Veterinary Clinical Sciences - Clinical Trials, Veterinary Medicines R&D, Veterinary Medicines Registration, Biostatistics
Reid, Jacky
NewMetrica
Fintry Rd
FK8 3HL Kippen
UK

Research - developing scientifically robust structured questionnaire instruments to measure pain and health related quality of life in non verbal species
Richez, Pascal
TransPharm
42 chemin des Olivettes
34160 Saint Genies des Mourgues
FR
T: +33 672 21 17 95
pascal.richez@club-internet.fr

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)
Rowan, Tim
Rowdix Ltd.
Folly Hall
YO62 4LW Cawton, York
UK
M: +44 7825082170
tim_g_rowan@hotmail.com

Scientific & Clinical expertise for Product Development, Specialist in Pharmaceuticals, pharmacology, efficacy, safety, Animal Production
Sarasola, Patxi
ONDAX Scientific SL
Komentutxiki 28
20280 Hondarriba (Gipuzkoa)
ES
T: +34 94 36 46 087
M: +34 659 939 586
http://www.ondax-scientific.com
psarasola@ondax-scientific.com

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
Scherkl, Rudolf
Atillastrasse 150
12105 Berlin
DE
T: +49 30 756 59 498
M: +49 173 200 59 42
F: +49 40 380178 54668
rls@rlscherkl.de

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.
Schirvel, Christian
Vel-Vet Consulting
5 allée des amaryllis
F-69290 Saint Genis les Ollières
FR
T: +33 621652926
F: +33 956158825
christian@velvetconsultinggroup.net

Schwer, Heidi
Vetmedico BV
Gaubergstraat 4
1570 Vollezele
BE

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
Silva, Byron
8411, Morumbi Ave. – 7th Floor – Suite # 71 - Broo
Sao Paulo

T: +55 11 5531-7272
byron.silva@vetaffairs.com.br

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.
Tasker, John
Independent Veterinary Consultant
4 Thorny Way, Highfields Caldecote
CB23 7ZE Cambridge
UK

Clinical trials, Veterinary drug D&D, Veterinary drug registration, Pharmacovigilance, Scientific writing, Marketing and technical support
Vandaele (retired), Bill
BILLSUPPORT
rue G. Charlier 11/33
7500 Tournai
BE
T: +32 475240552
bill@billsupport.be

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
Verhoeve, Peter
Regivet BV
Broekstraat 4c
5688JW Spoordonk (Oirschot)
NL
T: +31(0)499 577 903
peter@regivet.com

Veterinary RA &RD including: - Complete Pharmaceutical Development (Part 2) - GCP trials (Cats, dogs, horses) - Expert reports Part 2, 3 and 4 - Drug Registration