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Buyer's Guide - Education & Training

Klifovet AG

Geyerspergerstr. 27,
D-80689 München,
Germany
Tel: +49-89-5800820
Fax: +49-89-58008215

Contact: Dr. Klaus Hellmann
www.klifovet.com

 

Located in the center of Europe, thinking globally: Klifovet AG is a Munich/ Germany-based veterinary CRO providing the animal health and animal nutrition industry with services covering all aspects of product development of veterinary medicinal products and feed additives:

• Strategic consultancy: partner search and project management for the complete product development phase: from the idea to the market

• SME, MUMS, scientific advice: we assure that you enjoy all justified benefits

• Regulatory consultancy: analyses and strategy, expert reports, negotiations with the authorities, dossier writing, electronic submissions

•  Pharmacovigilance services incl. QPPV and life cycle management

•  Studies: Planning and conduct of EU GLP/GCP-compliant veterinary safety and efficacy studies in all target animal species

•  QA and QM: Quality assurance and management including audits to GCP, GLP and GMP

•  Data entry, data management and statistics

•  Electronic Data Capture: STUDYBASE®, the validated study management software exclusively made for animal studies

•  Import and manufacturing of veterinary medicinal products and clinical study supplies to GMP: re-packaging, labelling, storage, EU QP release

•  EU representation as Qualified Person for GMP (QP) and Qualified Person for Pharmacovigilance (QPPV)

•  Seminars and trainings

KLIFOVET is certified to ISO 9001, holds EU-GMP accreditation and fully complies with VICH GCP. KLIFOVET won the prestigious Animal Pharm Award twice in 2006 (Best Supporting Role) and 2016 (Best CRO), showing our long term excellent performance for our clients.

Veterinary Research Management Ltd

Veterinary Research Management Ltd,
The Mews Studio,
Portland Road,
Malvern, Worcs
WR14 2TA
UK
Tel: +44 1684 568998 or
+44 7968 696683

info@vrm.uk.com
www.vrm.uk.com

Specialists in research management with proven expertise in project delivery. Our services include:

• Project management
• Registration expertise - NCE’s & generics
• Dose optimisation
• GLP/GCPv compliant test facilities
• Dose determination, dose confirmation, safety, efficacy, residues, bioequivalence & pK studies in livestock & companion animals
• Specialist parasitology expertise & parasite supply
• Multi-country field studies
In vitro studies
• Scientific writing - peer reviewed publication, editorials, expert statements, study reports & regulatory defence

VRM also represents Ridgeway Research Ltd (UK), Invetus Pty Ltd (Australia), Northwest Biopharm Ltd (Ireland), Vetspin S.r.l (Italy) and Cyton Biosciences (UK). Affiliations with these other organisations provide VRM with direct access to first-class test facilities across the world and an expert team of interdisciplinary scientists, to draw on as appropriate to deliver your project.

Cyton

Cyton Biosciences Ltd.
68 Macrae Road
Eden Office Park
Bristol
BS20 0DD
UK
Tel: +44 (0)1179 739 036

enquiries@cyton.com
www.cyton.com
Twitter.com/CytonBio
LinkedIn.com/company/Cyton-Biosciences

Expertise in depth

Cyton is a full-service animal health consultancy providing specialist multi-disciplinary technical expertise in quality, safety and efficacy, as well as regulatory affairs for the following product types:

  • Pharmaceuticals

  • Immunologicals

  • Feed additives

 

Our clients include 8 of the top 10 global animal health companies and we have an equally broad base of SME clients and start-up companies, giving us a wealth of varied experience and an appreciation of every client's uniqueness.

Our team

Cyton's veterinarians, chemists, toxicologists and regulatory experts are at liberty to work with any global contract research organisation or contract manufacturer, ensuring that product development projects are delivered to match our clients' specific needs.

Global support

Because we understand the importance of local expertise we work closely with our offices in Germany, the USA and China to fulfil our customers' needs and achieve their product registrations in their target markets.

Contact us

Cyton has the technical and regulatory expertise to negotiate any challenges during product development and registration. Please get in touch for a free initial consultation.

Triveritas

Head office: Bank Barn,
How Mill,
Brampton,
Cumbria,
CA8 9JY
UK
Tel: +44 (0) 845 123 2888

info@triveritas.com
www.triveritas.com

A global CRO offering state of the art technological data management resources in AH clinical studies. Triveritas Electronic Data Capture System, from Prelude Dynamics, is a web-based EDC system compliant with 21 CFR 11. From the input to the output of data, our comprehensive data collection form library offers adaptable solutions for specific study requirements and designs.

Our flexible approach uses innovative strategies to address timelines and budget.

Expertise includes: Full Product Development; VICH GCP Clinical Studies; Regulatory Affairs; Strategic Advice; Quality Assurance (GxP); Training; Project Management and Pharmacovigilance.

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