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List of health conferences, educations - cme : upcoming 1839

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Prise en charge et suivi du patient asthmatique (1 journée)

Ref: 20367 Tuesday September 23rd, 2014 - Saint-Brieuc FR

Objectifs : Faire le point sur la maladie asthmatique et sa prise en charge Maitriser les traitements et les stratégies thérapeutiques Savoir informer et éduquer le patient asthmatique dans le cadre des entretiens pharmaceutiques Programme : Rappels ...

Education: Pharmacy

Prise en charge et suivi du patient sous AVK (1 journée)

Ref: 20375 Tuesday September 23rd, 2014 - Nantes FR

Objectifs : Permettre au stagiaire d'approfondir leurs connaissances sur les AVK Savoir identifier les situations à risque au comptoir Maîtriser la structure de l’entretien pharmaceutique et en faciliter sa mise en place à l'officine Programme : Les AVK : ...

Education: Pharmacy

Live webinar Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR

Ref: 20514 Tuesday September 23rd, 2014 - Houston US

  Use promo code CGO20 to get 20% off if you register before 5th September   DESCRIPTION
Device manufacturers are required to establish and maintain a quality management system, where appropriate and applicable, including design ...

Conference & Seminar: Medicine

Live web conference Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR

Ref: 20521 Tuesday September 23rd, 2014 - Houston US

DESCRIPTION Device manufacturers are required to establish and maintain a quality management system, where appropriate and applicable, including design control.    This webinar is intended to provide guidance on understanding, interpreting, and implementing design control ...

Conference & Seminar: Medicine

Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR

Ref: 20531 Tuesday September 23rd, 2014 - Houston US

  Use promo code CGO20 to get 20% off if you register before 11th September     DESCRIPTION Device manufacturers are required to establish and maintain a quality management system, where appropriate and applicable, including design control. ...

Conference & Seminar: Medicine

Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR

Ref: 20548 Tuesday September 23rd, 2014 - Houston US

DESCRIPTION     Device manufacturers are required to establish and maintain a quality management system, where appropriate and applicable, including design control.    This webinar is intended to provide guidance on understanding, interpreting, and implementing design ...

Conference & Seminar: Medicine

Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR

Ref: 20562 Tuesday September 23rd, 2014 - Houston US

DESCRIPTION     Device manufacturers are required to establish and maintain a quality management system, where appropriate and applicable, including design control.    This webinar is intended to provide guidance on understanding, interpreting, and implementing design ...

Conference & Seminar: Medicine

Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR

Ref: 20571 Tuesday September 23rd, 2014 - Houston US

DESCRIPTION     Device manufacturers are required to establish and maintain a quality management system, where appropriate and applicable, including design control.    This webinar is intended to provide guidance on understanding, interpreting, and implementing design ...

Conference & Seminar: Medicine

Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR

Ref: 20589 Tuesday September 23rd, 2014 - Houston US

DESCRIPTION     Device manufacturers are required to establish and maintain a quality management system, where appropriate and applicable, including design control.    This webinar is intended to provide guidance on understanding, interpreting, and implementing design ...

Conference & Seminar: Medicine, Pharmacy

Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR

Ref: 20596 Tuesday September 23rd, 2014 - Houston US

DESCRIPTION     Device manufacturers are required to establish and maintain a quality management system, where appropriate and applicable, including design control.    This webinar is intended to provide guidance on understanding, interpreting, and implementing design ...

Conference & Seminar: Medicine

Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR

Ref: 20613 Tuesday September 23rd, 2014 - Houston US

DESCRIPTION     Device manufacturers are required to establish and maintain a quality management system, where appropriate and applicable, including design control.    This webinar is intended to provide guidance on understanding, interpreting, and implementing design ...

Conference & Seminar: Medicine

Webinar On The 510(k) Program: Substantial Equivalence In Premarket Notifications

Ref: 20502 Wednesday September 24th, 2014 - Online

This guidance was released on July 28, 2014. FDA developed this document to provide guidance about current review practices for premarket notifications (510(k)) submissions.

Conference & Seminar: Research, Bio-Technologies, Pharmacy

Live web conference Electronic Records & Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20522 Wednesday September 24th, 2014 - Houston US

DESCRIPTION With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records.  After several years of development and industry comments, 21 CFR ...

Conference & Seminar: Medicine, Pharmacy, Bio-Technologies

Electronic Records & Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20532 Wednesday September 24th, 2014 - Houston US

Use promo code CGO20 to get 20% off if you register before 11th September   DESCRIPTION With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance ...

Conference & Seminar: Medicine, Pharmacy, Bio-Technologies

Electronic Records & Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20538 Wednesday September 24th, 2014 - Houston US

DESCRIPTION     With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records.  After several years of development and industry ...

Conference & Seminar: Medicine, Bio-Technologies, Pharmacy

Electronic Records & Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20550 Wednesday September 24th, 2014 - Houston US

DESCRIPTION     With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records.  After several years of development and industry ...

Conference & Seminar: Medicine, Pharmacy, Bio-Technologies

Electronic Records & Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20563 Wednesday September 24th, 2014 - Houston US

DESCRIPTION     With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records.  After several years of development and industry ...

Conference & Seminar: Medicine, Pharmacy, Bio-Technologies

Electronic Records & Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20564 Wednesday September 24th, 2014 - Houston US

DESCRIPTION     With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records.  After several years of development and industry ...

Conference & Seminar: Pharmacy, Medicine, Bio-Technologies

Electronic Records & Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20572 Wednesday September 24th, 2014 - Houston US

DESCRIPTION     With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records.  After several years of development and industry ...

Conference & Seminar: Medicine, Pharmacy, Bio-Technologies

Electronic Records & Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20590 Wednesday September 24th, 2014 - Houston US

DESCRIPTION     With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records.  After several years of development and industry ...

Conference & Seminar: Medicine, Pharmacy, Bio-Technologies

Electronic Records & Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20597 Wednesday September 24th, 2014 - Houston US

DESCRIPTION     With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records.  After several years of development and industry ...

Conference & Seminar: Medicine, Bio-Technologies, Pharmacy

Implementing an FDA-Compliant Medical Device Design Control Including DHF, DHR, and DMR

Ref: 20604 Wednesday September 24th, 2014 - Houston US

DESCRIPTION     Device manufacturers are required to establish and maintain a quality management system, where appropriate and applicable, including design control.    This webinar is intended to provide guidance on understanding, interpreting, and implementing design ...

Conference & Seminar: Medicine

Electronic Records & Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20605 Wednesday September 24th, 2014 - Houston US

DESCRIPTION     With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records.  After several years of development and industry ...

Conference & Seminar: Medicine, Pharmacy, Bio-Technologies

Electronic Signatures, 21 CFR Part 11 , Basic Concept

Ref: 20614 Wednesday September 24th, 2014 - Houston US

DESCRIPTION     With the emerging utilization of computerized technologies in the late 1980s and early 1990s, the pharmaceutical industry asked the FDA for guidance regarding compliance of the resulting electronic records.  After several years of development and industry ...

Conference & Seminar: Medicine, Bio-Technologies, Pharmacy

Live Webinar on FDA Adverse Event Reporting for Drugs and Medical Devices

Ref: 20501 Thursday September 25th, 2014 - Online

This web seminar presents an overview of FDA’s Adverse Event Reporting Systems for Drugs and Medical Devices.

Conference & Seminar: Bio-Technologies, Research, Pharmacy

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