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During the last 17 year Set- up and monitoring of more than 50 efficacy and mode of action trials for registration purposes was my main occupation. Those studies were set up in broilers, layers, pigs, turkey, dairy cattle and calves, with veterinary and feed additives. The products investigated covered a wide range namely probiotics, ecto- and endo- parasiticides, coccidiostats, antibiotics, organic acids and electrolytes. Further a resistance study monitoring Streptococcus faecium & Streptococcus faecalis sensitivity in pigs and poultry was initiated In feed stability trials and carcass quality trials served an European registration. Market research studies for coccidiostats and antibiotics were completed. Assessment of veterinary registration files and an efficacy expert opinion used in a registration dossier for EFSA were made. Further I was expert for application on efficacy for feed additives. Expert Food safety 5th and 6 th E.U. framework programme. Project technical assistant for 5th E.U. framework programme.


Current Experience

  • owner

    Sint-Gillis-Waas, België
    Since October 2014
    Efficacy trials

    -Advise a veterinary phamaceutical company on 1) possible experts for the completion of a dossier 2) The market for pre and probiotics in poultry for fattening product positioning possibilities. 3) desinfectants

    -Expert opinion on a registration dossier for pigeons

    -Advise for the set up of EU efficacy trials for a probiotic in dogs: gestating and lactating bitches, pups, adult dogs. write up of protocols. 

    -Consultation on the different legislation EU / US for the use and authorisation of micro-organisms in feed  


Past Experience


BrightOwl Assessment :
DependabilityOrganizationDiligenceAuthenticityInterest in knowledgeCuriosityPerspectiveResiliencyOptimism
Self Assessment :
EfficiencyAdaptabilityOptimismCreative thinkingInterest in knowledgeIndependence


BrightOwl Assessment :
EnglishFrenchProject ManagementClinical trial designMonitoring Study ProgressUnderstand how results translate to practiceUnderstand levels of research evidencedutch
Self Assessment :
RespiratoryInfectious diseasesUnderstand levels of research evidenceEnglishPatient Screening and RecruitmentProject ManagementPhase IVPhase IIIClinical trial budgetingMonitoring Study ProgressICH GCP guidelinesEfficacy trialsDeveloping Clinical Trial ProtocolsClinical trial designRandomization and blindingUnderstand how results translate to practiceInterpret clinical trial resultsSearch literature on clinical trials
LinkedIn Assessment :
efficacy trials in animalsSales ManagementRegistrationVeterinaryAnimal HealthPoultryFood SafetyRegulatory affairsAgricultureR&DAnimal NutritionAnimalsDogsscienceSwineBiotechnologyVeterinary MedicinePharmaceutical IndustryToxicologymolecular biologyFEEDIngredientsPetsInfectious diseasesClient EducationFood IndustryVaccinesEfficacyVirologyAnimal WelfareAnimal WorkImmunologyPharmaceutical salesLaboratoryPlant BreedingCattleGood Laboratory Practice (GLP)Regulatory submissionsPharmacokineticsAgribusinessClinical researchLifesciencesDrug DevelopmentClinical DevelopmentMarket researchAnimal HusbandryAnimal BehaviorEpidemiologyPharmacovigilanceClinical trials

Skills and Expertise

BrightOwl Assessment :
Interpret datalifescienceCreates a collaborative team environmentExecute scientific projectscoordinating research projectsCoach staffDirect co-workersGuide staffLiaise with research teamSolve problemsCollaboration
Self Assessment :
Act as the main line of communication between the sponsor and the investigatorAdminister, maintain and co-ordinate the logistical aspects of clinical trialsArchive trial documentation and correspondence.Assemble regulatory applicationsAttend at steering committee meetingsAttend seminars, courses and meetings within and outside the companyCollect data as required by the protocol and complete case report forms and reviews for completeness.Conduct literature searches.Design the studyDiscuss the results of testing with medical statisticiansDevelop protocolsDirect co-workers to achieve resultEnsure all clinical trials are executed in compliance with international GCP guidelines/regulations and SOPsgenerate Clinical Trial Report and manuscript for publicationmarketingSupervise and/or distribute trial supplies, including the trial drug


  • Dr.Med.Vet & Lic Zootechnie in Veterinary Sciences/Veterinary Clinical Sciences, General from Universiteit Gent in 1981
  • in veterinary medicine from Universiteit Gent in 1973

Training and Certification

  • expert EFSA in 2012 Certification
  • expert FAVV in 2006 Certification


BrightOwl Assessment:
Self Assessment:
Professional Proficiency
Professional Proficiency
Professional Proficiency

Work Preferences

  • Notice Period:
    4 weeks
  • Work From Home:
    Yes, 1 to 3 days per week
  • Work Regime:
    BrightOwl freelancer :    32 Hours per week
  • International:


    Expert has 1 publications (Will be avalible with full profile)

Area / Region

De Klinge


Driving License
  • Yes


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