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Regulations

clinique ovo and ovo r&d offer an extensive training program and continuous certifications to all its employees involved in research and development activities.

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    clinique ovo montreal

    All services offered 8000, boul. Décarie,
    Montreal Qc H4P 2S4
    ovo fertility office 100 & 200
    Monday to Friday 7:30am to 6:00pm
    Weekend on appointment
    fertilite@cliniqueovo.com
    ovo elle bureau 600
    Monday to Friday 8:00am to 4:00pm
    elle@cliniqueovo.com
    ovo cryo Monday to Wed. 8:00am to 5:00pm
    Thursday 8:00am to 6:00pm
    Friday 8:00am to 5:00pm
    Saturday 9:00am to 3:00pm
    Appointments :
    Monday to Friday 9:00am to 3:00pm
    Thursday 9:00am to 4:00pm
    Saturday 9:00am to 2:30pm
    cryo@cliniqueovo.com
    ovo biosurance office 600
    Monday to Friday 8:00am to 4:00pm
    biosurance@cliniqueovo.com
    ovo labo office 600
    Monday to Friday 8:00am to 4:00pm
    labo@cliniqueovo.com
    ovo prenatal office 600
    Monday to Friday 8:00am to 4:00pm
    prenatal@cliniqueovo.com
    ovo r&d office 600
    Monday to Friday 7:15am to 5:00pm
    r-d@cliniqueovo.com

    clinique ovo rive-sud

    3141, boul. Taschereau,
    Greenfield Park Qc J4V 2H2
    ovo fertility - certain services offered office 410
    Call to know our hours
    fertilite@cliniqueovo.com
    ovo prenatal - certain services offered office 420
    Monday to Friday 8:00am to 4:00pm
    prenatal@cliniqueovo.com
    ovo labo - certain services offered office 420
    Monday to Friday 8:00am to 4:00pm
    labo@cliniqueovo.com

    clinique ovo quebec

    ovo prenatal - certain services offered 2600 Boul. Laurier, suite 295,
    Quebec Qc G1V 4T3
    Monday to Friday 8:00am to 4:00pm prenatal@cliniqueovo.com



    clinique ovo rive-nord

    ovo prenatal - Prenatal screening 1000 Montée des Pionniers,
    Terrebonne QC J6V 1S8
    Monday to Thursday 9:00am to 3:00pm
    prenatal@cliniqueovo.com
    Montreal and South-Shore: t. 514.798.2000
    Quebec: t. 418.425.0128
    f. 514.798.2001

GCP: Good Clinical Practice – Quality Norms

All research members, including doctors and personnel, have been trained on Good Clinical Practices and meet these standards daily. A recertification of the GCP is done every 2 years.

Good Clinical Practice (GCP) is an international standard of ethical and scientific quality which applies to the design and implementation of trials involving human subjects and the recording and presentation of data. Respect of such a standard provides public assurance that the rights, safety and welfare of subjects participating in the trials are protected in accordance with the principles derived from the Declaration of Helsinki, and that the clinical data is reliable.

IATA and WHMIS: Handling and Transport of hazardous materials

Many research studies require shipment of biological products and shipment of hazardous materials by courier. In that effect, all research employees participate in a training regarding handling of hazardous materials (WHMIS) and shipping of hazardous materials (IATA).

WHMIS represents the data processing on hazardous materials used Canada-wide. IATA is the International Airport Transport Association. This association emits the norm regarding air transport security. These norms have also been applied to ground shipping in many countries.

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Ethics committee: validation and approval of research studies

Respect and patient safety is crucial in research. For this reason, every studies conducted by ovo r&d are reviewed and approved by an independent Review Board (IRB). This committee is composed of experts in ethics, external members, physicians and employees knowledgeable in the methods or research domains. Oversees the ethical nature of the study, the compliance to the protocol as well as patient safety.

If you are currently participating in a research project and have questions regarding your rights as a participant in a study; if you would like to discuss with someone that has no ties to the research study; or if you would like to form a complaint you can communicate with the person in charge at (514) 798-2000 ext 756. This person will transfer your contact information to the president of the ethics committee.

Health Canada

Every research project involving the use of medication (off-label medication, new dose) has to be submitted and reviewed by Health Canada. Health Canada has the right to visit research study sites that they have approved. Health Canada requirements in regards to documentation and structure are very elevated. Our research and development department aim for the highest quality standards. We develop and regulate all our research projects according to the norms and requirements of Health Canada, whether the studies are of interventional or observational nature.

ovo r&d has been audited by Health Canada in February 2012. Our research and development department has gained recognition and is compliant with Health Canada norms and requirements.